Vitamin B6 deficiency cooperates with oncogenic Ras to induce malignant tumors in Drosophila

Pilesi, Eleonora; Tesoriere, Giulia; Ferriero, Angelo; Mascolo, Elisa; Liguori, Francesco; Argirò, Luca; Angioli, Chiara; Tramonti, Angela; Contestabile, Roberto; Volontè, Cinzia; Vernì, Fiammetta

doi:10.1038/s41419-024-06787-3

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Published: 03 June 2024

Vitamin B6 deficiency cooperates with oncogenic Ras to induce malignant tumors in Drosophila

Cell Death & Disease volume 15, Article number: 388 (2024) Cite this article

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Abstract

Vitamin B6 is a water-soluble vitamin which possesses antioxidant properties. Its catalytically active form, pyridoxal 5’-phosphate (PLP), is a crucial cofactor for DNA and amino acid metabolism. The inverse correlation between vitamin B6 and cancer risk has been observed in several studies, although dietary vitamin B6 intake sometimes failed to confirm this association. However, the molecular link between vitamin B6 and cancer remains elusive. Previous work has shown that vitamin B6 deficiency causes chromosome aberrations (CABs) in Drosophila and human cells, suggesting that genome instability may correlate the lack of this vitamin to cancer. Here we provide evidence in support of this hypothesis. Firstly, we show that PLP deficiency, induced by the PLP antagonists 4-deoxypyridoxine (4DP) or ginkgotoxin (GT), promoted tumorigenesis in eye larval discs transforming benign Ras^V12 tumors into aggressive forms. In contrast, PLP supplementation reduced the development of tumors. We also show that low PLP levels, induced by 4DP or by silencing the sgll^PNPO gene involved in PLP biosynthesis, worsened the tumor phenotype in another Drosophila cancer model generated by concomitantly activating Ras^V12 and downregulating Discs-large (Dlg) gene. Moreover, we found that Ras^V12 eye discs from larvae reared on 4DP displayed CABs, reactive oxygen species (ROS) and low catalytic activity of serine hydroxymethyltransferase (SHMT), a PLP-dependent enzyme involved in thymidylate (dTMP) biosynthesis, in turn required for DNA replication and repair. Feeding Ras^V12 4DP-fed larvae with PLP or ascorbic acid (AA) plus dTMP, rescued both CABs and tumors. The same effect was produced by overexpressing catalase in Ras^V12 Dlg^RNAi 4DP-fed larvae, thus allowing to establish a relationship between PLP deficiency, CABs, and cancer. Overall, our data provide the first in vivo demonstration that PLP deficiency can impact on cancer by increasing genome instability, which is in turn mediated by ROS and reduced dTMP levels.

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Introduction

The catalytically active form of vitamin B6, pyridoxal 5′-phosphate (PLP), is an essential cofactor for a wide range of metabolic reactions mostly regulating amino acid biosynthesis and catabolism [1, 2]; in addition, PLP participates, as a cofactor of serine hydroxymethyltransferase (SHMT), to one-carbon (1 C) metabolism, involved in DNA synthesis and methylation processes [3]. Furthermore, vitamin B6 can quench reactive oxygen species (ROS) [4,5,6] and it regulates both abiotic and biotic stress of plants [7]. In animals, PLP is recycled from food in a salvage pathway requiring the action of pyridoxal kinase (PDXK) and pyridoxine 5’-phosphate oxidase (PNPO) enzymes [8]. Vitamin B6 is present in most foods, therefore a primary deficiency is uncommon in developed countries. However, a deficiency of vitamin B6 can develop as a secondary effect of several common pathologies including diabetes, celiac disease and bowel syndrome [8]. In addition, PLP deficiency is a condition often associated with pregnancy and can originate as a side effect of many common drugs including antibiotics such as isoniazid, penicillamine and cycloserine [9].

Vitamin B6 has been inversely associated to the risk and/or survival of several cancers [10]. Reduced serum levels of PLP, as well as impaired functional vitamin B6 status, as evaluated by the 3-hydroxykynurenine: xanthurenic acid ratio (HK:XA), have been for instance related to lung cancer risk [11,12,13]. Consistently, high expression levels of PDXK have been positively correlated to survival of non-small cell lung cancer (NSCLC) patients [14]. Low levels of plasmatic PLP have been related also to colon-rectal cancer (CRC) risk in several studies [15,16,17,18,19], while high levels have been associated with improved survival among CRC patients [20].

In contrast, previous observational studies of dietary or dietary plus supplementary intake of vitamin B6 and CRC risk reported nonsignificant positive or inverse associations [21, 22]. However a recent meta-analysis [23] including new studies [24, 25] resolved this discrepancy.

Works performed in mice and rats have shown that dietary vitamin B6 suppresses colon [26] and mammary tumorigenesis [27], thus indicating that animal models may help overcome limits and bias often associated to human research and, more importantly, can give the possibility to elucidate molecular links.

Based on multiple roles of vitamin B6, several mechanisms have been proposed to explain its impact on cancer. In particular, it is thought that PLP deficiency may compromise DNA synthesis [28], alter methylation pattern [29], promote angiogenesis [30], increase oxidative stress [31], promote inflammation [32] and impair anti-tumor immunity [33]. However, the molecular basis of these mechanisms has yet to be elucidated.

We and other authors have shown that PLP deficiency causes chromosome aberrations (CABs) in yeast, Drosophila and human cells [34, 35]. In particular, we proved that CABs originate from both oxidative stress [35] and impaired SHMT activity which in turn reduces thymidylate (dTMP) biosynthesis [36]. This finding led us to speculate that genome instability may link vitamin B6 with tumors. Consistent with this hypothesis, we also found that two PLP antagonists, 4-deoxypyridoxine (4DP) and ginkgotoxin (GT), induce the development of epithelial cancers on the adult cuticle of flies by promoting the loss of heterozygosity at the tumor suppressor warts (wts) locus [37].

In this work we used Drosophila melanogaster to investigate the possible role of vitamin B6 deficiency in cancer. Drosophila is emerging as a valuable model to study multiple aspects of tumor formation and malignant transformations, due to the conservation of most signaling pathways involved in cancer; in addition, flies are easy to manipulate genetically and have limited genetic redundancy. Most cancer research in Drosophila relied on the MARCM (mosaic analysis with repressible cell marker) strategy [38]. This allows, by mitotic recombination, the generation of clones expressing a constitutively active form of Ras85D (Ras^V12) that are, at the same time, mutants for tumor suppressors and marked with the green florescent protein (GFP), for easy visualization. The Ras^V12 overexpression leads to benign hyperplastic growth [39] thus, seminal works using MARCM method identified mutations in genes involved in apical–basal polarity and in genes with mitochondrial functions or involved in autophagy that cooperate with Ras^V12 to promote malignant traits [40,41,42,43]. In addition, several studies have successfully generated Drosophila models for lung, colorectal, brain and thyroid cancer, and for cancers that have been proven amenable to pharmacologic approaches [44,45,46].

In the present work we exploited the advantages of using flies to study the possible role of vitamin B6 deficiency in tumor onset or development and to identify molecular links mainly correlated to genome stability.

Results

Effect of PLP deficiency on Ras^V12 Drosophila cancer model

We previously demonstrated that Drosophila melanogaster is a suitable model to study the impact of vitamin B6 on human health [35, 47]. Here, we investigated the possible role of vitamin B6 deficiency in transforming benign Ras^V12 in malignant forms of tumor, based on the notion that cancer is a multistep process [48]. Using the MARCM strategy [38] we generated larvae (hereinafter named Ras^V12 larvae) in which clones expressing both Ras^V12 and the green fluorescent protein (GFP) were produced on eye-antennal discs by an eyeless-specific flippase enzyme (ey-FLP) via somatic recombination.

PLP deficiency was induced by feeding Ras^V12 larvae with the PLP antagonist 4-deoxypyridoxine (4DP [49]). As a control, in addition to Ras^V12 larvae reared on a standard medium, we generated larvae expressing only the GFP protein in eye disc clones, to monitor possible effects of 4DP on GFP expression. 4DP feeding leads to a 3-day delay in completion of larval development [47]. Thus, third instar Ras^V12 4DP-fed larvae were examined at 11 days after egg laying (AEL) and compared to Ras^V12 larvae at 8 days AEL. As reported in Fig. S1 older larval age of Ras^V12 4DP larvae did not influence the phenotype. 4DP feeding did not significantly alter GFP expression in control larvae (Fig. 1A, B). In contrast, it stimulated the proliferation of eye disc clones in Ras^V12 larvae, thus increasing the percentage of GFP-positive eye field area/ total body area with respect to control diet (10% vs 6%) (Fig. 1A, B). Accordingly, eye disc cells from Ras^V12 4DP larvae stained for phospho-Histone H3 (pH3), a specific marker for mitotic cells, displayed an increased mitotic index (MI) (Fig. 1E, F).

**Fig. 1: PLP deficiency cooperates with *Ras*^V12 in tumorigenesis.**

Feeding Ras^V12 larvae with gingkotoxin (GT), another PLP antagonist of PLP synthesis [49], yielded the same results (Fig. 1A, B), thus confirming the specificity of the effect. In contrast, PLP administration prevented tumor development (Fig. 1A, B), further reinforcing the role of PLP deficiency in Ras^V12 tumor transformation.

Ras^V12 larvae treated with PLP antagonists displayed secondary tumors far from the cephalic region (Fig. 1A). To quantify them, we analyzed the invasions on the larval brain ventral nerve cord (VNC) according to [41] and found that 4DP feeding caused VNC invasions in 29% of examined brains vs 4.1% in controls. GT treatment yielded VNC invasions (21.7%), whereas, in contrast, PLP supplementation strongly reduced migration (6.4%) (Fig. 1C, D).

We also tested 4DP on a cancer model in which Ras^V12 was expressed in all cells of the eye disc, finding the same results (Fig. S2).

Basement membrane (BM) degradation represents a crucial early step in the onset of cell spreading and metastasis [50]. Thus, to further confirm the association between PLP deficiency and secondary tumors, we assayed the BM integrity in eye discs from Ras^V12 4DP-fed larvae. The immunostaining with an anti-Perlecan antibody which represents a major BM component [51] yielded localized loss of Perlecan (Fig. 2A, B). Moreover, Ras^V12 4DP eye discs displayed an accumulation of Mmp1, a matrix metalloproteinase involved in BM breakdown [50] (Fig. 2C, D and S3), thus suggesting that vitamin B6 deficiency enhances the BM breakdown to facilitate the spreading of transformed cells.

**Fig. 2: PLP deficiency causes basement membrane degradation and promotes GFP-cells migration through hemolymph.**

It has been shown in Drosophila that cancer cells can move from the primary tumor site and travel through the hemolymph (a fluid analogous to blood) to reach secondary sites [52].

Consistently, we found that 54% of Ras^V12 4DP-fed larvae displayed GFP cells into the hemolymph (Fig. 2E, F). In contrast, GFP cells were found only in the hemolymph of 8% of Ras^V12 larvae reared on a control diet and never found in control larvae (expressing only the GFP) reared on 4DP or on a control diet. By considering that not all the cells floating in the hemolymph are able to settle in distant sites [52] these results are in line with those of VNC invasions (Fig. 1C, D) and suggest that 4DP feeding can favor the migration of GFP cells through the hemolymph, allowing those who find suitable conditions to colonize distant sites.

PLP deficiency exacerbates the cancer phenotype of Ras ^V12 Dlg ^RNAi tumors

To confirm the role of vitamin B6 deficiency in cancer, we used also another fly cancer model (Ras^V12 Dlg^RNAi), in which the expression of Ras^V12 in the entire eye-antennal disc, combined with the RNAi-induced silencing of Discs large (Dlg) polarity gene, produces neoplastic tumors able to metastasize [41]. 4DP feeding further enlarged the cephalic area of Ras^V12 Dlg^RNAi larvae compared to control diet (13.4% vs 10%) (Fig. 3A, B) and produced VNC invasions in 85% of brains (vs 48.6%) (Fig. 3C, D). 4DP induced a more aggressive phenotype compared to the control diet, yielding a higher percentage of severe (Type 3) VNC invasions (Fig. 3C). In contrast, PLP feeding significantly reduced the phenotype (Fig. 3 A, B, D) In addition, we genetically induced PLP deficiency by silencing the sgll^PNPO gene involved in PLP biosynthesis [53]. Consistent with the effect produced by 4DP, we found an increased cephalic area (13.8%) and VNC invasion in 66.6% of brains (Fig. 3D).

**Fig. 3: PLP deficiency increases proliferation and malignancy of *Ras*^V12Dlg^RNAi tumors.**

Overall, these data indicate that PLP deficiency also impacts on this second cancer model, by specifically increasing the malignancy of Ras^V12Dlg^RNAi tumors and triggering tumor progression.

PLP deficiency causes chromosome damage in Ras ^V12 eye discs

PLP depletion causes chromosome aberrations (CABs) in Drosophila, yeast, and human cells [35, 34, 54]. As CABs are well-known hallmarks of tumor initiation and progression [55], genome instability could play a major role in cancer induced by PLP deficiency. To test the validity of this hypothesis, we firstly examined eye discs from Ras^V12 4DP-fed larvae for the presence of chromosome damage in DAPI-stained preparations, finding 10.2% of CABs vs 1.4% in untreated Ras^V12 larvae (Fig. 4A, B). Of note, 4DP treatment combined to Ras^V12 expression produced a higher effect (10.2%) than the sum of the individual conditions (4DP 3%; Ras^V12 1,4%) (Chi square test, P < 0.001), thus suggesting that chromosome damage in Ras^V12 4DP discs may result from a synergistic interaction between PLP deficiency and the activated Ras (Fig. 4B). CABs were also found in Ras^V12Dlg^RNAi eye discs from larvae reared in 4DP and were rescued by PLP (Fig. 4A, B).

**Fig. 4: PLP deficiency causes CABs and accumulation of γ-H2Av foci in *Ras*^V12 and *Ras*^V12Dlg^RNAi eye discs.**

Consistent with the notion that CABs result from improperly repaired DNA double strand breaks (DSBs) [56], 4DP treatment produced an accumulation γ-H2Av, a marker of DSBs [57], in both Ras^V12 and Ras^V12Dlg^RNAi tumor cells (Fig. 4 C, D).

PLP treatment in addition to rescue tumor development (Figs. 1 and 3) also rescued CABs in eye discs from Ras^V12 and Ras^V12Dlg^RNAi 4DP-fed larvae (Fig. 4 A, B). More interestingly, overexpression of Catalase involved in endogenous ROS scavenging [58] rescued 4DP-induced CABs, DSBs and tumors in the Ras^V12Dlg^RNAi model (Fig. 4 and S4), thus providing robust indication that CABs may play a causative role in tumors induced by PLP depletion.

PLP deficiency causes ROS accumulation and reduced activity of SHMT in Ras ^V12 eye discs

We previously demonstrated in Drosophila that CABs resulting from PLP deficiency derive in part from ROS accumulation and in part from decreased dTMP availability, in turn caused by reduced SHMT catalytic activity [35, 36]. This is consistent with the role of vitamin B6 as antioxidant molecule [59,60,61,62] and with its role as a cofactor of SHMT, whose reaction yields 1 C units that ultimately produce thymidylate (dTMP) required for DNA synthesis and repair [3]. To investigate if the origin of CABs was the same also in PLP deficient Ras^V12 cells, we examined eye discs from Ras^V12 4DP-fed larvae by evaluating ROS accumulation and measuring the catalytic activity of SHMT. As shown in Fig. 5 A, B, dihydroethidium (DHE) staining revealed that eye discs from Ras^V12 4DP-fed larvae accumulated, in GFP-labeled clones, more ROS compared to Ras^V12 discs from larvae reared on a control diet. In contrast, feeding Ras^V12 4DP-treated larvae with the antioxidant ascorbic acid (AA) or PLP counteracted the formation of ROS (Fig. 5A, B). In addition, eye discs from 4DP-fed Ras^V12 larvae displayed a reduced catalytic activity of SHMT, compared to discs from Ras^V12 larvae fed a standard diet (Fig. 5D and S5). Given the role of SHMT in folate cycle this result suggests that discs from Ras^V12 4DP-fed larvae undergo a reduced biosynthesis of dTMP (Fig. 5C).

**Fig. 5: PLP deficiency causes ROS formation and reduced activity of SHMT in *Ras*^V12 eye discs.**

Role of oxidative stress and reduced activity of SHMT in tumors induced by PLP deficiency

To better correlate the oxidative stress and the reduced activity of SHMT with tumors induced by PLP deficiency and to shed light on their relative contributes, we fed flies with AA and dTMP alone or in combination, finding a complete rescue of both CABs and primary tumors, which further confirmed the role of CABs in 4DP-induced cancers (Fig. 6A-C and S6). CAB frequency decreased from 9.92% to 0.59% (Fig. 6C), the percentage of GFP-labeled area decreased from 9.25% to 4.42% (Fig. 6A, B), and the frequency of VNC invasions decreased from 29% to 7.7% (Fig. 6D).

**Fig. 6: The combined effect of ROS accumulation and dTMP depletion promotes both genome instability and cancer development in *Ras*^V12 4DP eye discs.**

Feeding Ras^V12 4DP larvae with AA yielded a complete rescue of both chromosome damage (CABs=0.54%) (Fig. 6C and S6), primary and secondary tumors (cephalic area=4.71%; VNC invasions= 8.0%) (Fig. 6A, B, D). The same effect was obtained with alpha-lipoic acid, another strong antioxidant (Fig. S7). Supplementation with dTMP produced a less pronounced rescue of CABs with respect to AA (2.45%) (Fig. 6C and S6), and a reduction of the area occupied by primary (6.6%) (Fig. 6A, B) and secondary tumors (VNC invasions =10.2%) (Fig. 6D).

Taken together these results suggested that both SHMT depletion and ROS accumulation may have a role in CAB production induced by PLP deficiency in Ras^V12, and also that they may synergize to increase the genome instability, thus predisposing cells to malignant transformation. Since dTMP is involved in DNA metabolism, its depletion may compromise the repair of lesions caused by ROS. Furthermore, in agreement with previous studies indicating that the knockout of SHMT2 increases ROS production in human cancer cells [63], dTMP supplementation reduced DHE staining of about 50% (Fig. 6E, F) in eye discs from Ras^V12 4DP-fed larvae, thus suggesting that under PLP deficiency dTMP depletion, may also contribute to increase the oxidative stress, besides compromising repair (Fig. 6G).

In conclusion, altogether, these results provide robust evidence that vitamin B6 deficiency can impact on Ras^V12 cancers and that this effect may be mediated by increased genome instability, in turn produced by the concerted action of ROS accumulation and decreased dTMP biosynthesis.

Discussion

Our study, carried out in Drosophila, provides the first compelling evidence that vitamin B6 deficiency affects cancer by promoting genome instability. In addition, it identifies two main mechanisms by which genome damage is produced in PLP deficient cells: increased ROS formation and reduced SHMT activity.

Several studies inversely correlated micronutrient plasma levels and human cancer risk. However, although many micronutrients are potential cancer promoting candidates because of their functional and biochemical properties, the establishing of a precise cause-effect relationship between diet and cancer in both observational epidemiological studies and intervention trials has proved challenging [64]. Using animal models may enable not only to establish these relationships more clearly, but also to identify underlying molecular mechanisms.

Among the animal cancer models, the common fruit fly is emerging as a precious resource for cancer biology and metabolic studies [65], since it offers a valuable toolkit with various advantages including high genetic conservation of major metabolic and cancer pathways and similar drug response to mammals.

Here we have shown that PLP deficiency, induced by 4DP feeding, is able to transform benign Ras^V12 cancers in more aggressive forms capable of generating secondary tumors as demonstrated by (i) migration of GFP cells into the brain VNC, (ii) membrane basement degradation, (iii) accumulation of Mmp1, and (iv) presence of GFP cells into the hemolymph of Ras^V12 4DP-fed larvae. The finding that even ginkgotoxin (GT), another antagonist of PLP [66], is able to transform Ras^V12 tumors further corroborates our results.

In addition, we have shown that PLP deficiency can also impact on the Ras^V12 Dlg^RNAi cancers, worsening their aggressiveness. Interestingly, the specific depletion of Sgll^/PNPO in Ras^V12Dlg^RNAi eye discs displayed the same effect as 4DP feeding, allowing us to exclude a major role of systemic effects of 4DP on cancer phenotypes.

Although several studies were focused on the involvement of vitamin B6 in cancer [10, 22], the underlying mechanisms are still elusive. We and other authors have previously demonstrated that PLP deficiency yields CABs and micronuclei in Drosophila and human cells, respectively, thus suggesting that genome instability may mediate the role of PLP in cancer [35, 54]. CABs can, indeed, provide growth benefits to precancerous cells or promote cancer progression by impacting on the formation of hybrid genes or the deletion of tumor suppressor genes [67, 68]. Here we have shown that eye discs from Ras^V12 4DP-fed larvae displayed CABs, accumulated ROS and exhibited a reduced SHMT catalytic activity, in line with previous studies indicating that CABs originate from oxidative stress and reduced dTMP biosynthesis in PLP deficient cells [35, 36]. Additionally, we provided robust evidence that CABs represent a major cause of tumors in PLP deficient larvae. By acting on the mechanisms that generate CABs in PLP depleted cells (such as ROS accumulation and dTMP depletion), we fed larvae with a diet made of AA+dTMP, finding a rescue of both CABs and tumors. Furthermore, overexpressing the Catalase gene in Ras^V12Dlg^RNAi tumor cells we also found that both 4DP-induced CABs and tumors were strongly reduced.

To investigate the relative roles of ROS accumulation and SHMT depletion in 4DP-induced tumors, we have supplied AA and dTMP separately. The complete rescue obtained with AA diet suggests that dTMP works downstream to ROS or, alternatively, that dTMP biosynthesis plays only a modest role. However, the finding that dTMP diet can rescue CABs and tumors would favor the first hypothesis. Thus, based on the role of dTMP in DNA synthesis and repair and on our finding that dTMP diet decreases ROS accumulation, we propose the following model that links, PLP deficiency, CABs, and cancer together (Fig. 5G).

Due to the ability of PLP to scavenge ROS both directly and indirectly [8], in PLP-deficient cells, weakened cellular antioxidant defenses, would increase the production of ROS, which attack DNA leading to the formation of DSBs, thus predisposing cells to cancer. Meanwhile, a reduced availability of PLP cofactor would reduce the biosynthesis of dTMP by affecting the catalytic activity of SHMT, thus amplifying the oxidative stress by both altering the repair of DNA ROS-induced lesions and increasing the production of ROS. Regarding the effect of dTMP depletion on the ROS increase, we do not have a molecular explanation, however our results are consistent with studies showing that inhibitors of thymidylate synthase, the enzyme directly involved in dTMP biosynthesis (Fig. 5C), can increase intracellular ROS by activating the enzyme NADPH oxidase and promoting apoptosis [69]. Similarly, the mitochondrial SHMT2 knockdown in bladder cancer cells leads to ROS accumulation and apoptosis [63]. We can, therefore, hypothesize that, in our model, 4DP treatment causes a less severe reduction of dTMP synthesis compared to SHMT knockdown or to a TS inhibition, thus allowing some cells with DNA damage to escape apoptosis and go towards cancer transformation.

Although we did not examine secondary tumors for chromosome damage, the finding that AA and dTMP diets alone or in combination rescue the phenotype may anyhow suggest that genome instability triggered by the concerted action of dTMP depletion and ROS increase may also contribute to the spread of tumor cells.

In this work, we considered only CABs and DSBs as genome damage endpoint, however we expect that a part of genome instability depends also on mutations due to DNA base oxidation (such as 8-oxo-2’-deoxyguanosine, 8 oxo-dG) and erroneous incorporation of dUTP into DNA. In line with this hypothesis, vitamin B6 in mice significantly suppressed colon cancer induced by azoxymethane (AOM) by decreasing levels of oxidative stress markers including 8 oxo-dG [31]. Moreover, cytosolic SHMT1 knockdown increased dUTP incorporation in lung cancer cells [70].

Finally, we can also hypothesize that the decreased catalytic activity of SHMT due to PLP deficiency may also alter the chromatin methylation patterns, thus contributing to Ras^V12 transformation [71]; this hypothesis will be tested in future studies.

In conclusion, we were able to demonstrate, for the first time, that PLP deficiency triggers cancer development in Drosophila and more importantly, we identified genome instability as an important player. Although vitamin B6 is present in most foods and hence an overt deficiency of this vitamin is rare, reduced PLP levels are associated with several common pathologies including diabetes and malabsorption syndromes [8]. Thus, applied to humans, our results may suggest the importance of evaluating the genome integrity as a biomarker of cancer risk factor in all the contexts of reduced availability of vitamin B6.

Materials and methods

Fly stocks

y,w eyFlp; Act > y + > Gal4 UAS GFP; FRT82B, Tub Gal80 was kindly provided by T. Xu lab (Yale School of Medicine).

UAS Ras^V12/ UAS Ras^V12; FRT82B/ FRT82B was kindly provided by Hirabayashi lab (London, Institute of Medical Science).

eyflp; UAS-Ras^V12, UAS-Dlg^RNAi/CyO, Gal80; act > CD2>Gal4, UAS-GFP and eyflp; Sp/CyO,Gal80; act4 > CD2>Gal4, UAS-GFP stocks were obtained by K. Basler (Institute of Molecular Life Sciences, University of Zurich, Switzerland). The sgll RNAi line (# 105941) was obtained by VDRC stock center (Vienna). The stockw[1]; P{w[+mC]=UAS-Cat.A}2 (Bl #24621) was obtained by Bloomington Indiana Stock Center.

Oregon-R was used as control wild type stock.

The balancers used in this work and the genetic markers are described in detail on FlyBase (http://flybase.bio.indiana.edu/).

Genetic Crosses

To generate larvae with clonal Ras^V12 tumors in eye-antennal discs we crossed:

y,w eyFlp; Act > y + > Gal4 UAS GFP; FRT82B, Tub Gal80 females to UAS Ras^V12/ UAS Ras^V12; FRT82B/ FRT82B males.
To generate control larvae expressing in clonal way only the GFP in the eye discs we crossed y,w eyFlp; Act > y + >Gal4 UAS GFP; FRT82B, Tub Gal80 females to Cy/Sco; FRT82B/TM6B,Tb males.
To generate larvae carrying Ras^V12 Dlg^RNAi tumors we crossed

eyflp; UAS-Ras^V12, UAS-Dlg ^RNAi/CyO, Gal80; act > CD2>Gal4, UAS-GFP females to Oregon-R males.
To test the effect of sgll^PNPO silencing on Ras^V12 Dlg^RNAi tumors, we crossed:

eyflp; UAS-Ras^V12, UAS-Dlg ^RNAi/CyO, Gal80; act > CD2>Gal4, UAS-GFP females to males from the sgll RNAi line (VDRC # 105941).
Control larvae expressing GFP in the entire eye-antennal disc were obtained by crossing:

eyflp; Sp/CyO,Gal80; act4 > CD2>Gal4, UAS-GFP females to Oregon-R males.
Control larvae to test the effect of Sgll depletion on GFP expression were obtained by crossing eyflp; Sp/CyO,Gal80; act4 > CD2>Gal4, UAS-GFP females to sgll RNAi males.
To generate larvae expressing Ras^V12 in the entire eye discs we crossed eyflp; Sp/CyO,Gal80; act4 > CD2>Gal4, UAS-GFP females to UAS Ras^V12V/ UAS Ras^V12 males.
To generate Ras^V12Dlg^RNAi larvae overexpressing Catalase we crossed:

eyflp; UAS-Ras^V12, UAS-Dlg ^RNAi/CyO, Gal8 ; act > CD2>Gal4, UAS-GFP females to w[1]; P{w[+mC]=UAS-Cat.A}2 males.
To obtain control larvae expressing Catalase in a non-tumor background we crossed eyflp; Sp/CyO,Gal80; act4 > CD2>Gal4, UAS-GFP females to w[1]; P{w[+mC]=UAS-Cat.A}2 males.

Treatments

All stocks were maintained and crossed at 25 °C on a standard medium containing in 100 mL: 0.68 g agar, 6.52 g yeast, 3 g flour, 600 µL propionic acid, and 5.13 g sucrose.

PLP antagonists such as 4-deoxypyridoxine (4DP, Sigma Cat. No. D0501) and ginkgotoxin (GT, Sigma Cat. No. 89960), as well as pyridoxal 5’phosphate (PLP, Sigma Cat. No. P9255), were dissolved in the standard medium at 2 mM, 0.2 mM and 0.5 mM final concentrations, respectively. 4DP and PLP concentrations were chosen according to [35]; GT concentration according to [72].

Deoxythymidine monophosphate (dTMP, Merck Cat. No. T7004‐100MG) was dissolved in the standard medium at 200 μM concentration. This concentration was established by adapting the concentration used in in vitro experiments to the oral administration [36]. Ascorbic acid (Sigma Cat. No. A 5960) was dissolved to standard medium at a final concentration of 40 mM according to [73].

Alpha-lipoic acid (ALA, Sigma Cat. No. T1395) was added to medium at 2 mM concentration according to [35].

Analysis of larvae

Larvae were immobilized by keeping them for at least 4 hours in PBS at 4 °C, and then examined under the fluorescence microscope (Carl Zeiss -Thornwood, NY) equipped with an HBO100W mercury lamp and a cooled charged‐coupled device (CCD camera; Photometrics CoolSnap HQ). The GFP-labeled area measurements were performed on the acquired pictures using imageJ software.

Larvae from at least 5 independent experiments have been examined.

Analysis of isolated brains

Brains from wandering third-instar larvae were dissected in PBS, and the distribution patterns of GFP clones were examined in optical lobes and ventral nerve cords (VNCs) under the fluorescence microscope (Carl Zeiss). The invasions of GFP clones from their original sites (eye-antennal discs and optical lobes) to VNCs were considered secondary tumors. Brains from 3 independent experiments have been analyzed.

Chromosome cytology

To analyze chromosome aberrations (CABs), eye discs from third instar larvae were dissected in saline (NaCl 0.7%). Metaphases were exposed to colchicine (final concentration 10^-5M) for 1 hr. The eye discs were then incubated in the hypotonic solution (sodium citrate 0.5%) for 7 minutes, squashed in 45% acetic acid, frozen in liquid nitrogen and mounted in Vectashield H‐1200 with 4,6 diamidino‐2‐phenylindole (DAPI; Vector Laboratories, Burlingame, CA). Observations were carried out using a Zeiss Axioplan fluorescence microscope equipped with CCD camera (Photometrics CoolSnap HQ).

To assay the effect of AA, dTMP or AA+dTMP in vitro, eye discs dissected from Ras^V12 4DP third instar larvae were incubated in 2 ml of saline supplemented with 10% fetal bovine serum (FBS, Gibco BRL) for 4 hours with addition of 50 µM dTMP according to [36] or 5 mM AA. One hour before fixation colchicine (final concentration, 10⁻⁵ M) was added to the saline/FBS to collect metaphases. Discs were then fixed with the standard procedure above described.

To calculate the percentage of CABs we arbitrarily assigned only five CABs to each cell with multifragmented chromosomes.

Immunofluorescence

Eye imaginal discs from third instar larvae were dissected in PBS and fixed in a 4% formaldehyde solution for 30 minutes on a rotating wheel at RT. Fixed tissues were then washed twice in a PBS 0,3% Triton (PBT) solution for 10 minutes and blocked in a PBT 5% Normal Donkey Serum (NDS) solution for 45 minutes. Samples were incubated overnight at 4 °C with primary antibody solution.

The day after, eye discs were washed twice in PBT and then incubated for 3 hours in the dark with. After two 10-minutes washes, samples were incubated in a DAPI solution for 30 minutes to stain nuclei. Finally, once removed tissue debris, samples were mounted onto microscope slides in FluoroMount (Sigma, F4680) medium and then sealed with nail polish.

The primary antibodies were: rabbit anti-Perlecan (1:1000 diluted in PBT 1% NDS, a gift of L. Pierre, Institute Curie, Paris, France); mouse anti Mmp1 (a cocktail of antibodies against Mmp1 catalytic domain #3B8D12 and #5H7B11, from Developmental Studies Hybridoma Bank, 1:50 diluted in PBT 1% NDS, a gift of T. Vaccari, Università degli studi di Milano, Italy).

The secondary antibodies were: donkey anti-rabbit Alexa-555-conjugated (1:600 diluted in PBT 1% NDS, Thermo Fisher Scientific Cat. No. A31572); donkey anti-mouse Alexa Fluor 555-conjugated (1:600 diluted in PBT 1% NDS, Thermo Fisher Scientific Cat. No. A32773) and donkey anti-rabbit Alexa Fluor 647-conjugated (1:600 diluted in PBT 1% NDS, Thermo Fisher Scientific Cat. No. A32795).

Immunofluorescence analysis was performed through a confocal laser scanning microscope (LSM800, Zeiss, Jena, Germany) equipped with four laser lines: 405 nm, 488 nm, 561 nm, and 639 nm. For each imaginal disc at least ten slices were acquired through Z-stack technology. The brightness and contrast of the digital images were adjusted using Zeiss Zen software 3.0 blue edition (Zeiss, Jena, Germany) and Adobe Photoshop CS6 (Adobe, San Jose, CA, USA).

The rate of BM damage was measured by analyzing each slice of each imaginal disc, scoring 120 images for each experimental condition. Fluorescence intensity of Mmp1 on eye discs was measured using the Image J software.

Immunostaining for pH3 and γ-H2Av was performed on eye discs from third instar larvae dissected and fixed as described in [74]. After several rinses in phosphate buffered saline 0.1% Triton (PBS-T) eye disc preparations were incubated overnight at 4 °C with primary antibodies diluted in PBT. After two rinses in PBT primary antibodies were detected by incubation for 1 h with the appropriate secondary antibody. We used the following primary antibodies: rabbit anti-phospho-Histone H3 (pSer10) Sigma-Aldrich Cat. No. 06570 (1:50, a gift of M. Gatti, Sapienza University of Rome, Italy) and rabbit anti-Histone H2AvD pS137 (1:100; Rockland Cat. No. 600-401-914). Secondary antibody was Alexa Fluor 555-conjugated anti-rabbit (1:300 in PBT; Thermo Fisher Scientific Cat. No. A31572). Immunostained preparations were mounted in Vectashield H-1200. Observations were carried out using a Zeiss Axioplan fluorescence microscope equipped with CCD camera (Photometrics CoolSnap HQ). The γ-H2AV positive cells were quantified on the acquired pictures using Adobe Photoshop 2022 version 23.5.5.

Dihydroethidium (DHE) staining

To evaluate ROS accumulation, third instar larval eye-antennal imaginal discs were dissected in Schneiders medium (Gibco, Cat. No. 21720024) and incubated in 30uM Dihydroethidium (DHE) (Thermo Fisher Cat. No. D23107) in PBS dye solution for 5 minutes in a dark chamber, on orbital shaker at room temperature. DHE is oxidized by superoxide radical to form 2-hydroxyethidium which intercalates with DNA and provides signal at 550 nm in cells where ROS are produced [75]. After 3 washes in Schneiders medium and 1 wash in PBS on an orbital shaker at room temperature, discs were immediately mounted in DAPI Vectashield. Images were immediately captured using the confocal microscope. Quantification was performed by using ImageJ/Fiji plugin to count spots (Spot Counter Plug-in version 0.14) and was expressed as DHE positive puncta/eye disc area.

Analysis of GFP cells into the hemolymph

Hemolymph was extracted from 20 larvae as described in [76]. 20 µL of hemolymph was mixed on a slide with 5 µL of DAPI and examined under the fluorescence microscope at 20x magnification. GFP cells were counted on acquired pictures using Photoshop software (2022 v23.5.5).

SHMT activity measurement

Measurement of SHMT activity was performed using a radioisotope assay based on the ability of SHMT to catalyze the exchange of the pro‐2 S proton of glycine with solvent [77]. Protein extracts obtained from about 100 discs in 20 mM K‐phosphate, pH 7.2, containing 150 mM NaCl, 0.1% NP‐40 and 5 mM 2‐mercapto ethanol, were incubated with tritiated [23H] glycine (23 nmol/L) at 30 °C for 4 h and treated as previously described [78]. The experiment was repeated four times, duplicates were used each time and the radioactivity was normalized to total protein content, determined with Bradford’s assay.

Statistical analysis

All data are expressed as mean ± standard error of the mean (SEM) from at least three independent experiments. Statistical significance was performed using the unpaired two-tailed t-test or the Chi square test as indicated in each figure legend. P < 0.05 was considered significant. Statistical parameters of individual experiments (value of n, mean, SEM, P values) are reported in each figure legend.

Data availability

All data reported in this paper will be shared upon request.

References

Parra M, Stahl S, Hellmann H. Vitamin B₆ and its role in cell metabolism and physiology. Cells. 2018;7:84.
Article PubMed PubMed Central Google Scholar
Stach K, Stach W, Augoff K. Vitamin B6 in health and disease. Nutrients. 2021;13:3229.
Article CAS PubMed PubMed Central Google Scholar
Ducker GS, Rabinowitz JD. One-carbon metabolism in health and disease. Cell Metab. 2017;25:27–42.
Article CAS PubMed Google Scholar
Kannan K, Jain SK. Effect of vitamin B6 on oxygen radicals, mitochondrial membrane potential, and lipid peroxidation in H2O2-treated U937 monocytes. Free Radic Biol Med. 2004;36:423–8.
Article CAS PubMed Google Scholar
Stocker P, Lesgards J-F, Vidal N, Chalier F, Prost M. ESR study of a biological assay on whole blood: antioxidant efficiency of various vitamins. Biochim Biophys Acta. 2003;1621:1–8.
Article CAS PubMed Google Scholar
Knöckel J, Müller IB, Butzloff S, Bergmann B, Walter RD, Wrenger C. The antioxidative effect of de novo generated vitamin B6 in Plasmodium falciparum validated by protein interference. Biochem J. 2012;443:397–405.
Article PubMed Google Scholar
Havaux M, Ksas B, Szewczyk A, Rumeau D, Franck F, Caffarri S, et al. Vitamin B6 deficient plants display increased sensitivity to high light and photo-oxidative stress. BMC Plant Biol. 2009;9:130.
Article PubMed PubMed Central Google Scholar
Contestabile R, di Salvo ML, Bunik V, Tramonti A, Vernì F. The multifaceted role of vitamin B(6) in cancer: Drosophila as a model system to investigate DNA damage. Open Biol. 2020;10:200034.
Article CAS PubMed PubMed Central Google Scholar
Clayton PT. B6-responsive disorders: a model of vitamin dependency. J Inherit Metab Dis. 2006;29:317–26.
Article CAS PubMed Google Scholar
Galluzzi L, Vacchelli E, Michels J, Garcia P, Kepp O, Senovilla L, et al. Effects of vitamin B6 metabolism on oncogenesis, tumor progression and therapeutic responses. Oncogene. 2013;32:4995–5004.
Article CAS PubMed Google Scholar
Johansson M, Relton C, Ueland PM, Vollset SE, Midttun Ø, Nygård O, et al. Serum B vitamin levels and risk of lung cancer. JAMA. 2010;303:2377–85.
Article CAS PubMed Google Scholar
Zuo H, Ueland PM, Midttun Ø, Tell GS, Fanidi A, Zheng W, et al. Vitamin B6 catabolism and lung cancer risk: results from the Lung Cancer Cohort Consortium (LC3). Ann Oncol Off J Eur Soc Med Oncol. 2019;30:478–85.
Article CAS Google Scholar
Theofylaktopoulou D, Midttun Ø, Ueland PM, Meyer K, Fanidi A, Zheng W, et al. Impaired functional vitamin B6 status is associated with increased risk of lung cancer. Int J Cancer. 2018;142:2425–34.
Article CAS PubMed PubMed Central Google Scholar
Galluzzi L, Vitale I, Senovilla L, Olaussen KA, Pinna G, Eisenberg T, et al. Prognostic impact of vitamin B6 metabolism in lung cancer. Cell Rep. 2012;2:257–69.
Article CAS PubMed Google Scholar
Wei EK, Giovannucci E, Selhub J, Fuchs CS, Hankinson SE, Ma J. Plasma vitamin B6 and the risk of colorectal cancer and adenoma in women. J Natl Cancer Inst. 2005;97:684–92.
Article CAS PubMed Google Scholar
Le Marchand L, White KK, Nomura AMY, Wilkens LR, Selhub JS, Tiirikainen M. et al. Plasma levels of B vitamins and colorectal cancer risk: the multiethnic cohort study. Cancer Epidemiol Biomarkers Prev. 2009;18:2195–201.
Article PubMed PubMed Central Google Scholar
Lee JE, Li H, Giovannucci E, Lee I-M, Selhub J, Stampfer M, et al. Prospective study of plasma vitamin B6 and risk of colorectal cancer in men. Cancer Epidemiol Biomarkers Prev. 2009;18:1197–202.
Article CAS PubMed PubMed Central Google Scholar
Larsson SC, Orsini N, Wolk A. Vitamin B6 and risk of colorectal cancer: a meta-analysis of prospective studies. JAMA. 2010;303:1077–83.
Article CAS PubMed Google Scholar
Gylling B, Myte R, Schneede J, Hallmans G, Häggström J, Johansson I, et al. Vitamin B-6 and colorectal cancer risk: a prospective population-based study using 3 distinct plasma markers of vitamin B-6 status. Am J Clin Nutr. 2017;105:897–904.
Article CAS PubMed Google Scholar
Holowatyj AN, Ose J, Gigic B, Lin T, Ulvik A, Geijsen AJMR, et al. Higher vitamin B6 status is associated with improved survival among patients with stage I-III colorectal cancer. Am J Clin Nutr. 2022;116:303–13.
Article CAS PubMed PubMed Central Google Scholar
Zhang X-H, Ma J, Smith-Warner SA, Lee JE, Giovannucci E. Vitamin B6 and colorectal cancer: current evidence and future directions. World J Gastroenterol. 2013;19:1005–10.
Article CAS PubMed PubMed Central Google Scholar
Mocellin S, Briarava M, Pilati P. Vitamin B6 and cancer risk: a field synopsis and meta-analysis. J Natl Cancer Inst. 2017;109:1–9.
Article PubMed Google Scholar
Lai J, Guo M, Wang D, Liu K, Hu D, Li J. Association between Vitamin B6 and the risk of colorectal cancer: a meta-analysis of observational studies. Nutr Cancer. 2023;75:1281–94.
Article CAS PubMed Google Scholar
Huang C-Y, Abulimiti A, Zhang X, Feng X-L, Luo H, Chen Y-M, et al. Dietary B vitamin and methionine intakes and risk for colorectal cancer: a case-control study in China. Br J Nutr. 2020;123:1277–89.
Article CAS PubMed Google Scholar
Xu L, Fang Y-J, Che M-M, Abulimiti A, Huang C-Y, Zhang C-X. Association of serum pyridoxal-5’-phosphate, pyridoxal, and PAr with colorectal cancer risk: a large-scale case-control study. Nutrients. 2022;14:2389.
Article CAS PubMed PubMed Central Google Scholar
Komatsu S, Yanaka N, Matsubara K, Kato N. Antitumor effect of vitamin B6 and its mechanisms. Biochim Biophys Acta. 2003;1647:127–30.
Article CAS PubMed Google Scholar
Shimada D, Fukuda A, Kawaguchi H, Kato N, Yoshida H, Kanouchi H, et al. Effect of high dose of pyridoxine on mammary tumorigenesis. Nutr Cancer. 2005;53:202–7.
Article CAS PubMed Google Scholar
Ames BN. DNA damage from micronutrient deficiencies is likely to be a major cause of cancer. Mutat Res. 2001;475:7–20.
Article CAS PubMed Google Scholar
Selhub J. Folate, vitamin B12 and vitamin B6 and one carbon metabolism. J Nutr Health Aging. 2002;6:39–42.
CAS PubMed Google Scholar
Matsubara K, Komatsu S, Oka T, Kato N. Vitamin B6-mediated suppression of colon tumorigenesis, cell proliferation, and angiogenesis (review). J Nutr Biochem. 2003;14:246–50.
Article CAS PubMed Google Scholar
Komatsu S-I, Watanabe H, Oka T, Tsuge H, Kat N. Dietary vitamin B6 suppresses colon tumorigenesis, 8-hydroxyguanosine, 4-hydroxynonenal, and inducible nitric oxide synthase protein in azoxymethane-treated mice. J Nutr Sci Vitaminol (Tokyo). 2002;48:65–8.
Article CAS PubMed Google Scholar
Shen J, Lai C-Q, Mattei J, Ordovas JM, Tucker KL. Association of vitamin B-6 status with inflammation, oxidative stress, and chronic inflammatory conditions: the Boston Puerto Rican Health Study. Am J Clin Nutr. 2010;91:337–42.
Article CAS PubMed Google Scholar
Bargiela D, Cunha PP, Veliça P, Foskolou IP, Barbieri L, Rundqvist H, et al. Vitamin B6 metabolism determines T cell anti-tumor responses. Front Immunol. 2022;13:837669.
Article CAS PubMed PubMed Central Google Scholar
Kanellis P, Gagliardi M, Banath JP, Szilard RK, Nakada S, Galicia S, et al. A screen for suppressors of gross chromosomal rearrangements identifies a conserved role for PLP in preventing DNA lesions. PLoS Genet. 2007;3:e134.
Article PubMed PubMed Central Google Scholar
Marzio A, Merigliano C, Gatti M, Vernì F. Sugar and chromosome stability: clastogenic effects of sugars in vitamin B6-deficient cells. PLoS Genet. 2014;10:e1004199.
Article PubMed PubMed Central Google Scholar
Pilesi E, Angioli C, Graziani C, Parroni A, Contestabile R, Tramonti A, et al. A gene-nutrient interaction between vitamin B6 and serine hydroxymethyltransferase (SHMT) affects genome integrity in Drosophila. J Cell Physiol. 2023;238:1558–66.
Article CAS PubMed Google Scholar
Gnocchini E, Pilesi E, Schiano L, Vernì F. Vitamin B6 deficiency promotes loss of heterozygosity (LOH) at the Drosophila warts (wts) locus. Int J Mol Sci. 2022;23:1–11.
Article Google Scholar
Lee T, Luo L. Mosaic analysis with a repressible cell marker for studies of gene function in neuronal morphogenesis. Neuron. 1999;22:451–61.
Article CAS PubMed Google Scholar
Karim FD, Rubin GM. Ectopic expression of activated Ras1 induces hyperplastic growth and increased cell death in Drosophila imaginal tissues. Development. 1998;125:1–9.
Article CAS PubMed Google Scholar
Brumby AM, Goulding KR, Schlosser T, Loi S, Galea R, Khoo P, et al. Identification of novel Ras-cooperating oncogenes in Drosophila melanogaster: a RhoGEF/Rho-family/JNK pathway is a central driver of tumorigenesis. Genetics. 2011;188:105–25.
Article CAS PubMed PubMed Central Google Scholar
Pagliarini RA, Xu T. A genetic screen in Drosophila for metastatic behavior. Science. 2003;302:1227–31.
Article CAS PubMed Google Scholar
Ohsawa S, Sato Y, Enomoto M, Nakamura M, Betsumiya A, Igaki T. Mitochondrial defect drives non-autonomous tumour progression through Hippo signalling in Drosophila. Nature. 2012;490:547–51.
Article CAS PubMed Google Scholar
Manent J, Banerjee S, de Matos Simoes R, Zoranovic T, Mitsiades C, Penninger JM, et al. Autophagy suppresses Ras-driven epithelial tumourigenesis by limiting the accumulation of reactive oxygen species. Oncogene. 2017;36:5576–92.
Article CAS PubMed PubMed Central Google Scholar
Levine BD, Cagan RL. Drosophila lung cancer models identify trametinib plus statin as candidate therapeutic. Cell Rep. 2016;14:1477–87.
Article CAS PubMed PubMed Central Google Scholar
Bangi E, Ang C, Smibert P, Uzilov AV, Teague AG, Antipin Y, et al. A personalized platform identifies trametinib plus zoledronate for a patient with KRAS-mutant metastatic colorectal cancer. Sci Adv. 2019;5:eaav6528.
Article CAS PubMed PubMed Central Google Scholar
Munnik C, Xaba MP, Malindisa ST, Russell BL, Sooklal SA. Drosophila melanogaster: a platform for anticancer drug discovery and personalized therapies. Front Genet. 2022;13:949241.
Article CAS PubMed PubMed Central Google Scholar
Merigliano C, Mascolo E, La Torre M, Saggio I, Vernì F. Protective role of vitamin B6 (PLP) against DNA damage in Drosophila models of type 2 diabetes. Sci Rep. 2018;8:11432.
Article PubMed PubMed Central Google Scholar
Vogelstein B, Kinzler KW. The multistep nature of cancer. Trends Genet. 1993;9:138–41.
Article CAS PubMed Google Scholar
Kästner U, Hallmen C, Wiese M, Leistner E, Drewke C. The human pyridoxal kinase, a plausible target for ginkgotoxin from Ginkgo biloba. FEBS J. 2007;274:1036–45.
Article PubMed Google Scholar
Deryugina EI, Quigley JP. Matrix metalloproteinases and tumor metastasis. Cancer Metastasis Rev. 2006;25:9–34.
Article CAS PubMed Google Scholar
Murdoch AD, Dodge GR, Cohen I, Tuan RS, Iozzo RV. Primary structure of the human heparan sulfate proteoglycan from basement membrane (HSPG2/perlecan). A chimeric molecule with multiple domains homologous to the low density lipoprotein receptor, laminin, neural cell adhesion molecules, and epidermal grow. J Biol Chem. 1992;267:8544–57.
Article CAS PubMed Google Scholar
Hirabayashi S, Baranski TJ, Cagan RL. Transformed Drosophila cells evade diet-mediated insulin resistance through wingless signaling. Cell. 2013;154:664–75.
Article CAS PubMed PubMed Central Google Scholar
Mascolo E, Amoroso N, Saggio I, Merigliano C, Vernì F. Pyridoxine/pyridoxamine 5’-phosphate oxidase (Sgll/PNPO) is important for DNA integrity and glucose homeostasis maintenance in Drosophila. J Cell Physiol. 2020;235:504–12.
Article CAS PubMed Google Scholar
Wu X, Xu W, Zhou T, Cao N, Ni J, Zou T, et al. The role of genetic polymorphisms as related to one-carbon metabolism, vitamin B6, and gene-nutrient interactions in maintaining genomic stability and cell viability in Chinese breast cancer patients. Int J Mol Sci. 2016;17:1003.
Article PubMed PubMed Central Google Scholar
Solomon E, Borrow J, Goddard AD. Chromosome aberrations and cancer. Science. 1991;254:1153–60.
Article CAS PubMed Google Scholar
Natarajan AT, Obe G. Molecular mechanisms involved in the production of chromosomal aberrations. III. Restriction endonucleases. Chromosoma. 1984;90:120–7.
Article CAS PubMed Google Scholar
Merigliano C, Marzio A, Renda F, Somma MP, Gatti M, Vernì F. A role for the twins protein phosphatase (PP2A-B55) in the maintenance of drosophila genome integrity. Genetics. 2017;205:1151–67.
Article CAS PubMed Google Scholar
Park SY, Kim Y-S, Yang D-J, Yoo M-A. Transcriptional regulation of the Drosophila catalase gene by the DRE/DREF system. Nucleic Acids Res. 2004;32:1318–24.
Article CAS PubMed PubMed Central Google Scholar
Cabrini L, Bergami R, Fiorentini D, Marchetti M, Landi L, Tolomelli B. Vitamin B6 deficiency affects antioxidant defences in rat liver and heart. Biochem Mol Biol Int. 1998;46:689–97.
CAS PubMed Google Scholar
Ohta BK, Foote CS. Characterization of endoperoxide and hydroperoxide intermediates in the reaction of pyridoxine with singlet oxygen. J Am Chem Soc. 2002;124:12064–5.
Article CAS PubMed Google Scholar
Matxain JM, Padro D, Ristilä M, Strid A, Eriksson LA. Evidence of high *OH radical quenching efficiency by vitamin B6. J Phys Chem USA. 2009;113:9629–32.
Sbodio JI, Snyder SH, Paul BD. Regulators of the transsulfuration pathway. Br J Pharmacol. 2019;176:583–93.
Article CAS PubMed Google Scholar
Zhang Y, Liu Z, Wang X, Jian H, Xiao H, Wen T. SHMT2 promotes cell viability and inhibits ROS-dependent, mitochondrial-mediated apoptosis via the intrinsic signaling pathway in bladder cancer cells. Cancer Gene Ther. 2022;29:1514–27.
Article CAS PubMed Google Scholar
Mayne ST, Playdon MC, Rock CL. Diet, nutrition, and cancer: past, present and future. Nat Rev Clin Oncol. 2016;13:504–15.
Article PubMed Google Scholar
Jiang H, Kimura T, Hai H, Yamamura R, Sonoshita M. Drosophila as a toolkit to tackle cancer and its metabolism. Front Oncol. 2022;12:982751.
Article CAS PubMed PubMed Central Google Scholar
Salamon N, Gurgui C, Leistner E, Drewke C. Influence of antivitamins ginkgotoxin 5’-phosphate and deoxypyridoxine 5’-phosphate on human pyridoxine 5’-phosphate oxidase. Planta Med. 2009;75:563–7.
Article CAS PubMed Google Scholar
Bonassi S, Znaor A, Norppa H, Hagmar L. Chromosomal aberrations and risk of cancer in humans: an epidemiologic perspective. Cytogenet Genome Res. 2004;104:376–82.
Article CAS PubMed Google Scholar
Heng HHQ, Bremer SW, Stevens J, Ye KJ, Miller F, Liu G, et al. Cancer progression by non-clonal chromosome aberrations. J Cell Biochem. 2006;98:1424–35.
Article PubMed Google Scholar
Ozer U, Barbour KW, Clinton SA, Berger FG. Oxidative Stress and Response to Thymidylate Synthase-Targeted Antimetabolites. Mol Pharmacol. 2015;88:970–81.
Article CAS PubMed PubMed Central Google Scholar
Paone A, Marani M, Fiascarelli A, Rinaldo S, Giardina G, Contestabile R, et al. SHMT1 knockdown induces apoptosis in lung cancer cells by causing uracil misincorporation. Cell Death Dis. 2014;5:e1525.
Article CAS PubMed PubMed Central Google Scholar
Sharma S, Kelly TK, Jones PA. Epigenetics in cancer. Carcinogenesis. 2010;31:27–36.
Article CAS PubMed Google Scholar
Gnocchini E, Pilesi E, Schiano L, Vernì F. Vitamin B6 Deficiency Promotes Loss of Heterozygosity (LOH) at the Drosophila warts (wts) Locus. Int J Mol Sci. 2022;23:6087.
Article CAS PubMed PubMed Central Google Scholar
Bahadorani S, Bahadorani P, Phillips JP, Hilliker AJ. The effects of vitamin supplementation on Drosophila life span under normoxia and under oxidative stress. J Gerontol A Biol Sci Med Sci. 2008;63:35–42.
Article PubMed Google Scholar
Bonaccorsi S, Giansanti MG, Gatti M. Spindle assembly in Drosophila neuroblasts and ganglion mother cells. Nat Cell Biol. 2000;2:54–6.
Article CAS PubMed Google Scholar
Zhao H, Kalivendi S, Zhang H, Joseph J, Nithipatikom K, Vásquez-Vivar J, et al. Superoxide reacts with hydroethidine but forms a fluorescent product that is distinctly different from ethidium: potential implications in intracellular fluorescence detection of superoxide. Free Radic Biol Med. 2003;34:1359–68.
Article CAS PubMed Google Scholar
Musselman LP, Fink JL, Narzinski K, Ramachandran PV, Hathiramani SS, Cagan RL, et al. A high-sugar diet produces obesity and insulin resistance in wild-type Drosophila. Dis Model Mech. 2011;4:842–9.
Article CAS PubMed PubMed Central Google Scholar
Stover PJ, Chen LH, Suh JR, Stover DM, Keyomarsi K, Shane B. Molecular cloning, characterization, and regulation of the human mitochondrial serine hydroxymethyltransferase gene. J Biol Chem. 1997;272:1842–8.
Article CAS PubMed Google Scholar
Tramonti A, Cuyàs E, Encinar JA, Pietzke M, Paone A, Verdura S, et al. Metformin is a Pyridoxal-5’-phosphate (PLP)-competitive inhibitor of SHMT2. Cancers (Basel). 2021;13:4009.
Article CAS PubMed Google Scholar

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Acknowledgements

We are grateful to Prof. T. Xu, Prof. S. Hirabayashi, Prof. K. Basler. Prof. L. Pierre, Prof. M. Gatti and Prof. T. Vaccari for generous sharing of fly stocks and antibodies. We acknowledge BDSC and VDRC for fly stocks.

Funding

This research was supported by grants from Sapienza University of Rome: RP120172838CFF6C to FV, RM12117A610B653E to RC, RM122181618E2878 to RC, AR1221814CAC1326 to EP.

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These authors contributed equally: Eleonora Pilesi, Giulia Tesoriere.

Authors and Affiliations

Dept. of Biology and Biotechnology “Charles Darwin”, Sapienza University of Rome, 00185, Rome, Italy
Eleonora Pilesi, Giulia Tesoriere, Angelo Ferriero, Elisa Mascolo, Luca Argirò, Chiara Angioli & Fiammetta Vernì
Experimental Neuroscience and Neurological Disease Models, IRCCS Santa Lucia Foundation, 00143, Rome, Italy
Francesco Liguori & Cinzia Volontè
CNR, Institute for Systems Analysis and Computer Science, 00185, Rome, Italy
Francesco Liguori & Cinzia Volontè
Institute of Molecular Biology and Pathology, 00185, Rome, Italy
Angela Tramonti
Department of Biochemical Sciences “A. Rossi Fanelli”, Sapienza, University of Rome, 00185, Rome, Italy
Roberto Contestabile
Istituto Pasteur-Fondazione Cenci Bolognetti, Sapienza, University of Rome, 00185, Rome, Italy
Roberto Contestabile

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Eleonora Pilesi
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Giulia Tesoriere
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Angelo Ferriero
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Elisa Mascolo
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Francesco Liguori
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Luca Argirò
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Chiara Angioli
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Angela Tramonti
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Roberto Contestabile
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Cinzia Volontè
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Fiammetta Vernì
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Contributions

EP, GT, AF, EM, LA, and CA performed the experiments. FL and AT performed the experiments, analyzed, and interpreted the data. RC and CV analyzed and interpreted the data. FV designed the project, analyzed the data, and wrote the paper. All authors read and approved the final paper.

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Correspondence to Fiammetta Vernì.

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Pilesi, E., Tesoriere, G., Ferriero, A. et al. Vitamin B6 deficiency cooperates with oncogenic Ras to induce malignant tumors in Drosophila. Cell Death Dis 15, 388 (2024). https://doi.org/10.1038/s41419-024-06787-3

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Received: 20 December 2023
Revised: 26 May 2024
Accepted: 28 May 2024
Published: 03 June 2024
DOI: https://doi.org/10.1038/s41419-024-06787-3

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Vitamin B6 deficiency produces metabolic alterations in Drosophila
- Giulia Tesoriere
- Eleonora Pilesi
- Fiammetta Vernì
Metabolomics (2025)

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Introduction

Results

Effect of PLP deficiency on RasV12 Drosophila cancer model

PLP deficiency exacerbates the cancer phenotype of Ras V12 Dlg RNAi tumors

PLP deficiency causes chromosome damage in Ras V12 eye discs

PLP deficiency causes ROS accumulation and reduced activity of SHMT in Ras V12 eye discs

Role of oxidative stress and reduced activity of SHMT in tumors induced by PLP deficiency

Discussion

Materials and methods

Fly stocks

Genetic Crosses

Treatments

Analysis of larvae

Analysis of isolated brains

Chromosome cytology

Immunofluorescence

Dihydroethidium (DHE) staining

Analysis of GFP cells into the hemolymph

SHMT activity measurement

Statistical analysis

Data availability

References

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Funding

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Vitamin B6 deficiency produces metabolic alterations in Drosophila

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ZnT7 RNAi favors Raf^GOFscrib^−/−-induced tumor growth and invasion in Drosophila through JNK signaling pathway

Effect of PLP deficiency on Ras^V12 Drosophila cancer model

PLP deficiency exacerbates the cancer phenotype of Ras ^V12 Dlg ^RNAi tumors

PLP deficiency causes chromosome damage in Ras ^V12 eye discs

PLP deficiency causes ROS accumulation and reduced activity of SHMT in Ras ^V12 eye discs