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Current Computer-Aided Drug Design

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ISSN (Print): 1573-4099
ISSN (Online): 1875-6697

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Research Article

Investigation on the Anticancer Activity of [6]-Gingerol of Zingiber officinale and its Structural Analogs against Skin Cancer

Author(s): Monisha Adikesavan, Praveena Athiraja* and Monisha Baby Babu Divakar

Volume 20, Issue 4, 2024

Published on: 03 May, 2023

Page: [367 - 373] Pages: 7

DOI: 10.2174/1573409919666230418095105

Price: $65

Abstract

Introduction: Skin cancer is the most common type of cancer caused by the uncontrolled growth of abnormal cells in the epidermis and the outermost skin layer.

Aim: This study aimed to study the anti-skin cancer potential of [6]-Gingerol and 21 related structural analogs using in vitro and in silico studies.

Methods: The ethanolic crude extract of the selected plant was subjected to phytochemical and GC-MS analysis to confirm the presence of the [6]-gingerol. The anticancer activity of the extract was evaluated by MTT (3-[4, 5-dimethylthiazol-2-y]-2, 5-diphenyl tetrazolium bromide) assay using the A431 human skin adenocarcinoma cell line.

Results: The GC-MS analysis confirmed the presence of [6]-Gingerol compound, and its promising cytotoxicity IC50 was found at 81.46 ug/ml in the MTT assay. Furthermore, the in silico studies used [6]-Gingerol and 21 structural analogs collected from the PubChem database to investigate the anticancer potential and drug-likeliness properties. Skin cancer protein, DDX3X, was selected as a target that regulates all stages of RNA metabolism. It was docked with 22 compounds, including [6]-Gingerol and 21 structural analogs. The potent lead molecule was selected based on the lowest binding energy value.

Conclusion: Thus, the [6]-Gingerol and its structure analogs could be used as lead molecules against skin cancer and future drug development process.

Keywords: Skin cancer, lead compounds, Zingiber officinale, anticancer, molecular docking, [6]-Gingerol.

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[1]
Baba, A.I.; Câtoi, C. Tumor Cell Morphology Bucharest (RO) Comparative Oncology; The Publishing House of the Romanian Academy: Romania, 2007.
[2]
Hassanpour, S.H.; Dehghani, M. Review of cancer from perspective of molecular. J. Cancer Res. Pract., 2017, 4(4), 127-129.
[http://dx.doi.org/10.1016/j.jcrpr.2017.07.001]
[3]
Howell, J.Y.; Ramsey, M.L. Squamous Cell Skin Cancer; StatPearls, 2022.
[4]
Hueng, D.Y.; Tsai, W.C.; Chiou, H.Y.; Feng, S.W.; Lin, C.; Li, Y.F.; Huang, L.C.; Lin, M.H. DDX3X biomarker correlates with poor survival in human Gliomas. Int. J. Mol. Sci., 2015, 16(12), 15578-15591.
[http://dx.doi.org/10.3390/ijms160715578] [PMID: 26184164]
[5]
Mo, J.; Liang, H.; Su, C.; Li, P.; Chen, J.; Zhang, B. DDX3X: Structure, physiologic functions and cancer. Mol. Cancer, 2021, 20(1), 38.
[http://dx.doi.org/10.1186/s12943-021-01325-7] [PMID: 33627125]
[6]
Surh, Y.J.; Lee, E.; Lee, J.M. Chemoprotective properties of some pungent ingredients present in red pepper and ginger. Mutat. Res., 1998, 402(1-2), 259-267.
[http://dx.doi.org/10.1016/S0027-5107(97)00305-9] [PMID: 9675305]
[7]
Eliopoulos, C. Ginger: More than a great spice. Director, 2007, 15(1), 46-47.
[PMID: 19348054]
[8]
Nicoll, R.; Henein, M.Y. Ginger (Zingiber officinale Roscoe): A hot remedy for cardiovascular disease? Int. J. Cardiol., 2009, 131(3), 408-409.
[http://dx.doi.org/10.1016/j.ijcard.2007.07.107] [PMID: 18037515]
[9]
Rahman, G.; Syed Umer, J.; Syed, F.; Samiullah, S.; Nusrat, J. Preliminary phytochemical screening, quantitative analysis of alkaloids, and antioxidant activity of crude plant extracts from Ephedra intermedia indigenous to balochistan. Sci. World J.,, 2017, 2017, 5873648.
[http://dx.doi.org/10.1155/2017/5873648]
[10]
Bryan, CPG.; Elliot, S. C Ancient Egyptian medicine: the Papyrus Ebers; Ares Publishers, 2021.
[11]
Berman, H.M.; Westbrook, J.; Feng, Z.; Gilliland, G.; Bhat, T.N.; Weissig, H.; Shindyalov, I.N.; Bourne, P.E. The protein data bank. Nucleic Acids Res., 2000, 28(1), 235-242.
[http://dx.doi.org/10.1093/nar/28.1.235] [PMID: 10592235]
[12]
Kim, S.; Chen, J.; Cheng, T.; Gindulyte, A.; He, J.; He, S.; Li, Q.; Shoemaker, B.A.; Thiessen, P.A.; Yu, B.; Zaslavsky, L.; Zhang, J.; Bolton, E.E. PubChem in 2021: New data content and improved web interfaces. Nucleic Acids Res., 2021, 49(D1), D1388-D1395.
[http://dx.doi.org/10.1093/nar/gkaa971] [PMID: 33151290]
[13]
Eberhardt, J.; Santos-Martins, D.; Tillack, A.F.; Forli, S. Autodock vina 1.2.0: New docking methods, expanded force field, and python bindings. J. Chem. Inf. Model., 2021, 61(8), 3891-3898.
[http://dx.doi.org/10.1021/acs.jcim.1c00203] [PMID: 34278794]
[14]
Daina, A.; Michielin, O.; Zoete, V. SwissADME: A free web tool to evaluate pharmacokinetics, drug-likeness and medicinal chemistry friendliness of small molecules. Sci. Rep., 2017, 7(1), 42717.
[http://dx.doi.org/10.1038/srep42717] [PMID: 28256516]
[15]
Lee, C.S.; Dias, A.P.; Jedrychowski, M.; Patel, A.H.; Hsu, J.L.; Reed, R. Human DDX3 functions in translation and interacts with the translation initiation factor eIF3. Nucleic Acids Res., 2008, 36(14), 4708-4718.
[http://dx.doi.org/10.1093/nar/gkn454] [PMID: 18628297]
[16]
Park, Y.J.; Wen, J.; Bang, S.; Park, S.W.; Song, S.Y. [6]-Gingerolinduces cell cycle arrest and cell death of mutant p53-expressing pancreatic cancer cells. Yonsei Med. J., 2006, 47(5), 688-697.
[http://dx.doi.org/10.3349/ymj.2006.47.5.688]
[17]
Ortega, S.S.; Cara, L.C.L.; Salvador, M.K. In silico pharmacology for a multidisciplinary drug discovery process. Drug Metabol. Drug Interact., 2012, 27(4), 199-207.
[http://dx.doi.org/10.1515/dmdi-2012-0021] [PMID: 23152402]

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