A comprehensive systematic review of studies on the potential of A49T and V89L polymorphism in SRD5AR2 as high susceptibility gene association with benign prostate hyperplasia and prostate cancer.

IF 1.3 Q3 UROLOGY & NEPHROLOGY
Archivio Italiano di Urologia e Andrologia Pub Date : 2025-03-28 Epub Date: 2025-02-17 DOI:10.4081/aiua.2025.13318
Revina Maharani, Hotma Lestari, Putra Mahakarya Dewa, Dewangga Yudisthira, Nasim Amar, Besut Daryanto
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引用次数: 0

Abstract

Introduction and objectives: Being the most common disease in aged men, the etiology of benign prostatic hyperplasia (BPH) is not fully defined. Recent studies have reported that the association between BPH and metabolic genes is still inconsistent. A gene connected with BPH is SRD5AR2, whose polymorphisms, A49T and V89L, have distinct enzyme activity. This systematic review examines SRD5AR2 polymorphisms within two alleles (A49T and V89L), assessing their roles as prognostic indicators of malignancy, and response to medication.

Materials and methods: We conducted a search on six different databases, including PubMed, Scopus, Wiley, ProQuest, Cochrane Central, and Science Direct using as string of keywords (BPH) AND [(rs523349) OR (V89L)] AND [(rs9282858) OR (A49T)]. We finally selected seven articles to be extracted. Quality appraisal of clinical trials was evaluated using the Joanna Briggs Institute Approach for systematic reviews.

Results: We sorted nine clinical studies from various countries examining SRDA52 polymorphism and its association of BPH and prostate cancer. About V89L we found that the "LL" genotype, indicating reduced 5α-reductase activity, is linked to a lower BPH risk, while the "VV" genotype may slightly increase BPH risk. About A49T, compared to "AA" genotype, "AT" tends to be associated to higher risk in developing prostate cancer. A49T polymorphism does not show any effect on medical treatment while V89L showed a protective effect on the clinical progression of BPH when treated with 5a-reductase inhibitors, aadrenergic receptor antagonists, and alpha blockers.

Conclusions: SRD5A2 polymorphisms could be a good indicator for prognostic malignancy and a potential tool for personalized medicine of BPH. The findings strongly support the recommendation for further study about SRD5AR2 to enhance its use for screening and prevention and to optimize the medical treatment of BPH.

对SRD5AR2中A49T和V89L多态性作为良性前列腺增生和前列腺癌相关高易感基因的研究潜力进行全面系统综述。
简介与目的:良性前列腺增生(BPH)是老年男性最常见的疾病,其病因尚未完全明确。最近的研究报道,前列腺增生与代谢基因之间的关系仍然不一致。与BPH相关的基因是SRD5AR2,其多态性为A49T和V89L,具有不同的酶活性。本系统综述研究了两个等位基因(A49T和V89L)内的SRD5AR2多态性,评估了它们作为恶性肿瘤预后指标的作用以及对药物的反应。材料和方法:我们在PubMed、Scopus、Wiley、ProQuest、Cochrane Central、Science Direct等6个不同的数据库中进行检索,使用关键词字符串(BPH)和[(rss523349) OR (V89L)]和[(rs9282858) OR (A49T)]。我们最终选择了7篇文章进行提取。临床试验的质量评价采用乔安娜布里格斯研究所方法进行系统评价。结果:我们收集了来自各国的9项临床研究,研究了SRDA52多态性及其与BPH和前列腺癌的关系。关于V89L,我们发现“LL”基因型表明5α-还原酶活性降低,与较低的BPH风险相关,而“VV”基因型可能略微增加BPH风险。关于A49T,与“AA”基因型相比,“AT”基因型倾向于患前列腺癌的风险更高。A49T多态性对药物治疗没有任何影响,而V89L在5a-还原酶抑制剂、肾上腺素能受体拮抗剂和α受体阻滞剂治疗时对BPH的临床进展有保护作用。结论:SRD5A2基因多态性可作为判断恶性肿瘤预后的良好指标和BPH个体化治疗的潜在工具。这些发现有力地支持了进一步研究SRD5AR2的建议,以加强其在前列腺增生的筛查和预防中的应用,并优化其医学治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.10
自引率
35.70%
发文量
72
审稿时长
10 weeks
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