Lam Dilys, Clark Susan, Stirzaker Clare, Pidsley Ruth
Epigenetics Research Laboratory, Genomics and Epigenetics Division, Garvan Institute of Medical Research, Sydney, NSW 2010, Australia.
St. Vincent's Clinical School, University of New South Wales, Sydney, NSW 2010, Australia.
Cancers (Basel). 2020 Oct 15;12(10):2993. doi: 10.3390/cancers12102993.
There is a major clinical need for accurate biomarkers for prostate cancer prognosis, to better inform treatment strategies and disease monitoring. Current clinically recognised prognostic factors, including prostate-specific antigen (PSA) levels, lack sensitivity and specificity in distinguishing aggressive from indolent disease, particularly in patients with localised intermediate grade prostate cancer. There has therefore been a major focus on identifying molecular biomarkers that can add prognostic value to existing markers, including investigation of DNA methylation, which has a known role in tumorigenesis. In this review, we will provide a comprehensive overview of the current state of DNA methylation biomarker studies in prostate cancer prognosis, and highlight the advances that have been made in this field. We cover the numerous studies into well-established candidate genes, and explore the technological transition that has enabled hypothesis-free genome-wide studies and the subsequent discovery of novel prognostic genes.
对于前列腺癌预后的准确生物标志物存在重大临床需求,以便更好地指导治疗策略和疾病监测。目前临床上公认的预后因素,包括前列腺特异性抗原(PSA)水平,在区分侵袭性疾病和惰性疾病方面缺乏敏感性和特异性,尤其是在局限性中级前列腺癌患者中。因此,主要集中在识别能够为现有标志物增加预后价值的分子生物标志物,包括对在肿瘤发生中具有已知作用的DNA甲基化的研究。在本综述中,我们将全面概述前列腺癌预后中DNA甲基化生物标志物研究的现状,并强调该领域取得的进展。我们涵盖了对成熟候选基因的众多研究,并探讨了使无假设全基因组研究以及随后发现新的预后基因成为可能的技术转变。