Prostate Cancer: Advances in Genetic Testing and Clinical Implications

IF 0.4 Q4 MATHEMATICS, APPLIED
A. Abdelrazek, K. Ghoniem, Mohamed E. Ahmed, Vidhu B. Joshi, Ahmed M. Mahmoud, Nader Saeed, N. Khater, M. Elsharkawy, A. Gamal, E. Kwon, A. Kendi
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引用次数: 1

Abstract

The demand for genetic testing (GT) for prostate cancer (PCa) is expanding, but there is limited knowledge about the genetic counseling (GC) needs of men. A strong-to-moderate inherited genetic predisposition causes approximately 5–20% of prostate cancer (PCa). In men with prostate cancer, germline testing may benefit the patient by informing treatment options, and if a mutation is noticed, it may also guide screening for other cancers and have family implications for cascade genetic testing (testing of close relatives for the same germline mutation). Relatives with the same germline mutations may be eligible for early cancer detection strategies and preventive measures. Cascade family testing can be favorable for family members, but it is currently unutilized, and strategies to overcome obstacles like knowledge deficiency, family communication, lack of access to genetic services, and testing expenses are needed. In this review, we will look at the genetic factors that have been linked to prostate cancer, as well as the role of genetic counseling and testing in the early detection of advanced prostate cancer.
前列腺癌:基因检测和临床意义的进展
前列腺癌(PCa)基因检测(GT)的需求正在扩大,但对男性遗传咨询(GC)需求的了解有限。强至中度遗传易感性导致约5-20%的前列腺癌(PCa)。对于患有前列腺癌的男性,生殖系检测可以通过告知治疗方案使患者受益,如果发现突变,它也可以指导其他癌症的筛查,并具有级联基因检测的家庭意义(对近亲进行相同生殖系突变的检测)。具有相同种系突变的亲属可能有资格获得早期癌症检测策略和预防措施。级联家庭检测可能对家庭成员有利,但目前尚未得到利用,需要采取策略克服知识缺乏、家庭沟通、缺乏获得遗传服务的机会和检测费用等障碍。在这篇综述中,我们将探讨与前列腺癌有关的遗传因素,以及遗传咨询和检测在早期发现晚期前列腺癌中的作用。
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
0.80
自引率
20.00%
发文量
67
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