American Journal of Cancer Prevention
ISSN (Print): 2328-7314 ISSN (Online): 2328-7322 Website: https://www.sciepub.com/journal/ajcp Editor-in-chief: Nabil Abdel-Hamid
Open Access
Journal Browser
Go
American Journal of Cancer Prevention. 2023, 10(1), 14-20
DOI: 10.12691/ajcp-10-1-4
Open AccessArticle

The Prediagnosis of Prostate Cancer Risk is Possible with the Evaluation of BRCA1 Primary Exons in Men

Haboubacar Elhadji Yaou Moussa1, Maazou Halidou2, Sara Y. Houngue1, Josué Avakoudjo3, Solomon Oladapo Rotimi4 and Callinice D. Capo-Chichi1,

1Laboratory of Molecular Biomarkers in Cancer and Nutrition, Department of Biochemistry and Cellular Biology, University of Abomey Calavi

2Zinder National Hospital, Niger

3National Teaching Hospital (CNHU-HKM) Cotonou, Benin

4Biology Laboratory, Covenant University Ogun State, Nigeria

Pub. Date: July 19, 2023

Cite this paper:
Haboubacar Elhadji Yaou Moussa, Maazou Halidou, Sara Y. Houngue, Josué Avakoudjo, Solomon Oladapo Rotimi and Callinice D. Capo-Chichi. The Prediagnosis of Prostate Cancer Risk is Possible with the Evaluation of BRCA1 Primary Exons in Men. American Journal of Cancer Prevention. 2023; 10(1):14-20. doi: 10.12691/ajcp-10-1-4

Abstract

Prostate cancer is a public health concern among men older than 50 years worldwide and its incidence keep rising as younger men are now diagnosed with this affliction. It is triggered by genomic instability or epigenetic modifications impacting genes and proteins involved in DNA repair, cell growth regulation and tumor suppression. In sub-Saharan African countries, few data are available on prostate cancer and the loss of BRCA1function. Recent studies have associated BRCA1 mutations to prostate cancer. Men with prostate cancer have symptoms like nocturia, poor urinary flow, hematuria, erectile dysfunction all of which affect their familial and social life. The main objective of our study is to assess the association between the instability of BRCA1 primary exons and the occurrence of prostate cancer, with the motivation to contribute to its early prescreening, prevention and treatment. Thus, to assess the functionality of BRCA1 we have investigated the integrity of exon 1,2,3 and 5 in male diagnosed with prostate cancer in three west African countries (Benin, Nigeria and Niger). Materials and methods: Peripheral blood was collected from men diagnosed with prostate cancer in urological service of three hospitals respectively in Benin (n= 20), Nigeria (n= 16) and Niger (n = 20) subsequent to ethical comity authorization (CLERB-UP) and signed informed consent from participants. Control samples (n= 20) were from healthy male students and university professors older than 25 years. Chloroform/isoamyl alcohol method was used to extract DNA before quantification with spectrophotometer. Polymerase chain reaction (PCR) was used to amplify exon 1, 2, 3 and 5 from 50 ng DNA, before migration on 1% agarose gel. Results and discussion: In all samples exon 2 and exon 5 were not amplified in 31.34% and 31.63% respectively; while Exon 1 and exon 3 were not amplified in 17.53% and 19.5% respectively. All of which could be due to deletion or spontaneous mutation. Conclusion: BRCA1 mutation should also be investigate in routine exam for prostate cancer prevention and treatment in sub-Saharan African population to prescribed the proper drug accordingly.

Keywords:
prostate cancer pre-diagnostic BRCA1

Creative CommonsThis work is licensed under a Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

References:

[1]  Rotimi, S.O., O.A. Rotimi, and B. Salhia, A Review of Cancer Genetics and Genomics Studies in Africa. Frontiers in Oncology, 2021. 10(3239).
 
[2]  Organization, W.H., Cancer. February 2022.
 
[3]  Lozano, R., et al., Genetic aberrations in DNA repair pathways: a cornerstone of precision oncology in prostate cancer. British Journal of Cancer, 2021. 124(3): p. 552-563.
 
[4]  Savage, K.I. and D.P. Harkin, BRCA1, a 'complex' protein involved in the maintenance of genomic stability. Febs j, 2015. 282(4): p. 630-46.
 
[5]  Fenichel, P., N. Chevalier, and F. Brucker-Davis. Bisphenol A: an endocrine and metabolic disruptor. in Annales d'endocrinologie. 2013. Elsevier.
 
[6]  Gangkak, G., et al., Immunohistochemical analysis of estrogen receptors in prostate and clinical correlation in men with benign prostatic hyperplasia. Investig Clin Urol, 2017. 58(2): p. 117-126.
 
[7]  Koutros, S., et al., Risk of total and aggressive prostate cancer and pesticide use in the Agricultural Health Study. American journal of epidemiology, 2013. 177(1): p. 59-74.
 
[8]  Multigner, L., et al., Chlordecone exposure and risk of prostate cancer. Journal of clinical oncology, 2010. 28(21): p. 3457-3462.
 
[9]  Benzi, R., et al., Cooperativity flows and shear-bandings: a statistical field theory approach. Soft Matter, 2016. 12(2): p. 514-30.
 
[10]  Chu, L.W., et al., Prostate cancer incidence rates in Africa. Prostate cancer, 2011. 2011.
 
[11]  Bourke, L., et al., Lifestyle changes for improving disease-specific quality of life in sedentary men on long-term androgen-deprivation therapy for advanced prostate cancer: a randomised controlled trial. European urology, 2014. 65(5): p. 865-872.
 
[12]  Desgrandchamps, F. and L. Bastien, Nutrition, dietary supplements and prostate cancer. Progres en Urologie: Journal de L'association Francaise D'urologie et de la Societe Francaise D'urologie, 2010. 20(8): p. 560-565.
 
[13]  Diallo, A., et al., Associations between fruit, vegetable and legume intakes and prostate cancer risk: results from the prospective Supplémentation en Vitamines et Minéraux Antioxydants (SU.VI.MAX) cohort. Br J Nutr, 2016. 115(9): p. 1579-85.
 
[14]  Raimondi, S., et al., Diet and prostate cancer risk with specific focus on dairy products and dietary calcium: a case–control study. The Prostate, 2010. 70(10): p. 1054-1065.
 
[15]  Bonjour, J.P., T. Chevalley, and P. Fardellone, Calcium intake and vitamin D metabolism and action, in healthy conditions and in prostate cancer. Br J Nutr, 2007. 97(4): p. 611-6.
 
[16]  Elmets, C.A., et al., Chemoprevention of nonmelanoma skin cancer with celecoxib: a randomized, double-blind, placebo-controlled trial. J Natl Cancer Inst, 2010. 102(24): p. 1835-44.
 
[17]  Shang, Y., et al., Vasectomy and prostate cancer risk: a meta-analysis of cohort studies. Sci Rep, 2015. 5: p. 9920.
 
[18]  Seo, J.E., et al., Mechanistic Evaluation of Black Cohosh Extract-Induced Genotoxicity in Human Cells. Toxicol Sci, 2021. 182(1): p. 96-106.
 
[19]  Bistulfi, G., et al., Dietary folate deficiency blocks prostate cancer progression in the TRAMP model. Cancer Prevention Research, 2011. 4(11): p. 1825-1834.
 
[20]  Sun, F.V., Q.F. Hu, and G.W. Xia, [Roles of folate metabolism in prostate cancer]. Zhonghua Nan Ke Xue, 2015. 21(7): p. 659-62.
 
[21]  Pernar, C.H., et al., The Epidemiology of Prostate Cancer. Cold Spring Harb Perspect Med, 2018. 8(12).
 
[22]  Rizos, C., et al., Alcohol consumption and prostate cancer: a mini review. Exp Oncol, 2010. 32(2): p. 66-70.
 
[23]  Islami, F., et al., A systematic review and meta-analysis of tobacco use and prostate cancer mortality and incidence in prospective cohort studies. Eur Urol, 2014. 66(6): p. 1054-64.
 
[24]  Lozano, P., et al., U.S. Preventive Services Task Force Evidence Syntheses, formerly Systematic Evidence Reviews, in Lipid Screening in Childhood for Detection of Multifactorial Dyslipidemia: A Systematic Evidence Review for the U.S. Preventive Services Task Force. 2016, Agency for Healthcare Research and Quality (US): Rockville (MD).
 
[25]  FDA, U., FDA grants accelerated approval to rucaparib for BRCA-mutated metastatic castration-resistant prostate cancer (2020).
 
[26]  Couñago, F., et al., Clinical Applications of Molecular Biomarkers in Prostate Cancer. Cancers (Basel), 2020. 12(6).
 
[27]  Munteanu, V.C., et al., PSA Based Biomarkers, Imagistic Techniques and Combined Tests for a Better Diagnostic of Localized Prostate Cancer. Diagnostics (Basel), 2020. 10(10).
 
[28]  Rao, A.R., H.G. Motiwala, and O.M. Karim, The discovery of prostate-specific antigen. BJU Int, 2008. 101(1): p. 5-10.
 
[29]  Ahmad, S., et al. AGEs, RAGEs and s-RAGE; friend or foe for cancer. in Seminars in cancer biology. 2018. Elsevier.
 
[30]  Kim, I.E., Jr., et al., Abrogation of survival disparity between Black and White individuals after the USPSTF's 2012 prostate-specific antigen-based prostate cancer screening recommendation. Cancer, 2020. 126(23): p. 5114-5123.
 
[31]  Lepor, A., W.J. Catalona, and S. Loeb, The Prostate Health Index: Its Utility in Prostate Cancer Detection. Urol Clin North Am, 2016. 43(1): p. 1-6.
 
[32]  Cui, Y., et al., Evaluation of prostate cancer antigen 3 for detecting prostate cancer: a systematic review and meta-analysis. Sci Rep, 2016. 6: p. 25776.
 
[33]  Gargouri, H. and H. Hadj Kacem, Evaluation of alternative DNA extraction protocols for the species determination in turkey salami authentication tests. International Journal of Food Properties, 2018. 21(1): p. 733-745.
 
[34]  Nesbit, M.A., et al., Characterization of GATA3 Mutations in the Hypoparathyroidism, Deafness, and Renal Dysplasia (HDR) Syndrome*. Journal of Biological Chemistry, 2004. 279(21): p. 22624-22634.
 
[35]  Soulié, M., et al., Cancer of the prostate in France: Results of the survey CCAFU-FRANCIM. Progres en Urologie: Journal de L'association Francaise D'urologie et de la Societe Francaise D'urologie, 2001. 11(3): p. 478-485.
 
[36]  Klionsky, D.J., et al., Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)(1). Autophagy, 2021. 17(1): p. 1-382.
 
[37]  Sung, H., et al., Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J Clin, 2021. 71(3): p. 209-249.
 
[38]  Boussios, S., et al., Aberrations of DNA repair pathways in prostate cancer: a cornerstone of precision oncology. Expert Opin Ther Targets, 2021. 25(5): p. 329-333.
 
[39]  Ghose, A., et al., Genetic Aberrations of DNA Repair Pathways in Prostate Cancer: Translation to the Clinic. Int J Mol Sci, 2021. 22(18).
 
[40]  Hanahan, D. and R.A. Weinberg, Hallmarks of cancer: the next generation. Cell, 2011. 144(5): p. 646-74.
 
[41]  Nombela, P., et al., BRCA2 and Other DDR Genes in Prostate Cancer. Cancers (Basel), 2019. 11(3).
 
[42]  Hounnasso Pp, A.J., Aouagbe Behanzin Hg, Tandje Y, Ouake A, Alabi M, Hodonou R, Akpo C, ASPECTS DIAGNOSTIQUES DU CANCER DE LA PROSTATE DANS LE SERVICE D’UROLOGIE DU CNHU-HKM COTONOU. 2015. Uro’Andro - Volume 1 N° 4 Juillet 2015.
 
[43]  Amégbor, K., et al., [Epidemiology and histopronostic of prostatic cancer in Togo: about 202 cases diagnosed at the laboratory of pathology of the Tokoin teaching hospital of Lome]. Prog Urol, 2009. 19(2): p. 112-5.
 
[44]  Ammani, A., Profil épidémiologique du cancer de la prostate dans le service d’urologie de l’hôpital Mohammed V de Rabat. Journal Marocain d'Urologie, 2007. 1(5): p. 11-14.
 
[45]  Popiolek, M., et al., Natural history of early, localized prostate cancer: a final report from three decades of follow-up. Eur Urol, 2013. 63(3): p. 428-35.
 
[46]  Diallo, A., et al., Caractéristiques cliniques du cancer de la prostate en Guinée. Résultats sur la période 2000-2006. African Journal of Urology, 2007. 13(4): p. 280-287.
 
[47]  Manguoğlu, E., et al., Germline mutations of BRCA1 and BRCA2 genes in Turkish breast, ovarian, and prostate cancer patients. Cancer Genet Cytogenet, 2010. 203(2): p. 230-7.
 
[48]  Hu, X., et al., Prevalence and clinical significance of pathogenic germline BRCA1/2 mutations in Chinese non-small cell lung cancer patients. Cancer Biol Med, 2019. 16(3): p. 556-564.
 
[49]  Ling, D.C., J.A. Vargo, and S. Beriwal, Breast, prostate, and rectal cancer: Should 5-5-5 be a new standard of care? International Journal of Radiation Oncology, Biology, Physics, 2020. 108(2): p. 390-393.