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对SRD5AR2基因中A49T和V89L多态性作为与良性前列腺增生和前列腺癌相关的高易感性基因的研究进行全面系统综述。

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.

作者信息

Maharani Revina, Lestari Hotma, Dewa Putra Mahakarya, Yudisthira Dewangga, Amar Nasim, Daryanto Besut

机构信息

Medical Faculty, Universitas Brawijaya, Malang.

Urology Department, Faculty of Medicine Universitas Brawijaya; Dr. Saiful Anwar General Hospital, Malang.

出版信息

Arch Ital Urol Androl. 2025 Mar 28;97(1):13318. doi: 10.4081/aiua.2025.13318. Epub 2025 Feb 17.

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.

摘要

引言与目的

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。近期研究报道,BPH与代谢基因之间的关联仍不一致。与BPH相关的一个基因是SRD5AR2,其多态性A49T和V89L具有不同的酶活性。本系统评价研究了SRD5AR2基因在两个等位基因(A49T和V89L)内的多态性,评估它们作为恶性肿瘤预后指标以及对药物反应的作用。

材料与方法

我们在六个不同的数据库进行了检索,包括PubMed、Scopus、Wiley、ProQuest、Cochrane Central和ScienceDirect,使用关键词串“(BPH)AND [(rs523349)OR(V89L)] AND [(rs9282858)OR(A49T)]”。我们最终筛选出七篇文章进行提取。使用乔安娜·布里格斯研究所的系统评价方法对临床试验进行质量评估。

结果

我们整理了来自不同国家的九项临床研究,这些研究考察了SRDA52多态性及其与BPH和前列腺癌的关联。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”基因型可能会略微增加BPH风险。关于A49T,与“AA”基因型相比,“AT”基因型在前列腺癌发生中往往与较高风险相关。A49T多态性对药物治疗没有任何影响,而V89L在用5α-还原酶抑制剂、α肾上腺素能受体拮抗剂和α阻滞剂治疗时,对BPH的临床进展具有保护作用。

结论

SRD5A2多态性可能是恶性肿瘤预后的良好指标,也是BPH个性化医疗的潜在工具。这些发现强烈支持进一步研究SRD5AR2的建议,以加强其在筛查和预防中的应用,并优化BPH的药物治疗。

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