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Identification of new genetic risk factors for prostate cancer

机译:鉴定前列腺癌的新遗传危险因素

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摘要

There is evidence that a substantial part of genetic predisposition to prostate cancer (PCa) may be due to lower penetrance genes which are found by genome-wide association studies. We have recently conducted such a study and seven new regions of the genome linked to PCa risk have been identified. Three of these loci contain candidate susceptibility genes: MSMB, LMTK2 and KLK2/3. The MSMB and KLK2/3 genes may be useful for PCa screening, and the LMTK2 gene might provide a potential therapeutic target. Together with results from other groups, there are now 23 germline genetic variants which have been reported. These results have the potential to be developed into a genetic test. However, we consider that marketing of tests to the public is premature, as PCa risk can not be evaluated fully at this stage and the appropriate screening protocols need to be developed. Follow-up validation studies, as well as studies to explore the psychological implications of genetic profile testing, will be vital prior to roll out into healthcare.
机译:有证据表明,前列腺癌(PCa)遗传易感性的很大一部分可能是由于全基因组关联研究发现的较低的渗透性基因。我们最近进行了这样的研究,并且确定了与PCa风险相关的基因组的七个新区域。这些基因座中的三个含有候选易感基因:MSMB,LMTK2和KLK2 / 3。 MSMB和KLK2 / 3基因可能对PCa筛查有用,而LMTK2基因可能提供潜在的治疗靶点。连同其他研究小组的结果,目前已有23种种系遗传变异的报道。这些结果有可能发展成为基因测试。但是,我们认为向公众推销测试尚为时过早,因为在此阶段无法全面评估PCa风险,需要制定适当的筛查方案。后续验证研究以及探索基因概况测试的心理影响的研究对于将其推广到医疗保健领域至关重要。

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