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Association between single-nucleotide polymorphisms in growth factor genes and quality of life in men with prostate cancer and the general population

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Abstract

Purpose

Improved survival for men with prostate cancer has led to increased attention to factors influencing quality of life (QOL). As protein levels of vascular endothelial growth factor (VEGF) and insulin-like growth factor 1 (IGF-1) have been reported to be associated with QOL in people with cancer, we sought to identify whether single-nucleotide polymorphisms (SNPs) of these genes were associated with QOL in men with prostate cancer.

Methods

Multiple linear regression of two data sets (including approximately 750 men newly diagnosed with prostate cancer and 550 men from the general population) was used to investigate SNPs of VEGF and IGF-1 (10 SNPs in total) for associations with QOL (measured by the SF-36v2 health survey).

Results

Men with prostate cancer who carried the minor ‘T’ allele for IGF-1 SNP rs35767 had higher mean Role-Physical scale scores (≥0.3 SD) compared to non-carriers (p < 0.05). While this association was not identified in men from the general population, one IGF-1 SNP rs7965399 was associated with higher mean Bodily Pain scale scores in men from the general population that was not found in men with prostate cancer. Men from the general population who carried the rare ‘C’ allele had higher mean Bodily Pain scale scores (≥0.3 SD) than non-carriers (p < 0.05).

Conclusions

Through identifying SNPs that are associated with QOL in men with prostate cancer and men from the general population, this study adds to the mapping of complex interrelationships that influence QOL and suggests a role for IGF-I in physical QOL outcomes. Future research may identify biomarkers associated with increased risk of poor QOL that could assist in the provision of pre-emptive support for those identified at risk.

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Acknowledgments

The authors thank the many patients and control subjects for participating; the great contribution made by Diana Battistutta to this project; the members of the Cancer Council Queensland, particularly Megan Ferguson and Andrea Kittila; the hospitals that participated in recruitment for the ProsCan study: Greenslopes Private, Royal Brisbane, Mater Adults, Princess Alexandra, Ipswich, QEII, Redlands and Redcliffe Hospitals, Townsville General Hospital and Mackay Base Hospital; the QUT Prostate Cancer Program, particularly Patricia Vanden Bergh, Soulmaz Rostami, Naomi Richardson and Robert Smith, members from the QIMR Berghofer Molecular Cancer Epidemiology Laboratory and XiaoQing Chen and Jonathan Beesley from QIMR Berghofer. This research was funded by National Health and Medical Research Council (NHMRC) Grants 390130, 290456, 614296, 1009458. A number of authors are supported by NHMRC fellowships (J. Clements: NHMRC Principal Research Fellowship, M. Spurdle: NHMRC Senior Research Fellowship, J. Batra: NHMRC Early Career Fellowship and Institute of Health and Biomedical Innovation (IHBI) Fellowship and F. Lose: PCFA Funding, S. Chambers: NHMRC Career Development Award). K. Alexander was supported by an Australian Postgraduate Award and T. O’Mara was supported by an Australian Postgraduate Award, Queensland Government PhD Award and IHBI PhD Award.

Conflict of interest

The authors declare they have no conflict of interest.

Ethical Standards

The authors declare that the above research was approved by the Queensland University of Technology (QUT), QIMR Berghofer Medical Research Institute, Mater Hospital (for Brisbane Private Hospital), Royal Brisbane Hospital, Princess Alexandra Hospital and the Cancer Council Queensland Human Research Ethics Committees. All participants gave informed consent prior to the inclusion in this study.

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Correspondence to Kimberly E. Alexander.

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Alexander, K.E., Chambers, S., Spurdle, A.B. et al. Association between single-nucleotide polymorphisms in growth factor genes and quality of life in men with prostate cancer and the general population. Qual Life Res 24, 2183–2193 (2015). https://doi.org/10.1007/s11136-015-0950-6

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  • DOI: https://doi.org/10.1007/s11136-015-0950-6

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