Zelic R, Fiano V, Grasso C, Zugna D, Pettersson A, Gillio-Tos A, Merletti F, Richiardi L
Cancer Epidemiology Unit-CERMS, Department of Medical Sciences, University of Turin, and CPO-Piemonte, Turin, Italy.
Clinical Epidemiology Unit, Department of Medicine, Solna, Karolinska Institutet, Stockholm, Sweden.
Prostate Cancer Prostatic Dis. 2015 Mar;18(1):1-12. doi: 10.1038/pcan.2014.45. Epub 2014 Nov 11.
The role of global DNA methylation in prostate cancer (PCa) remains largely unknown. Our aim was to summarize evidence on the role of global DNA hypomethylation in PCa development and progression.
We searched PubMed through December 2013 for all studies containing information on global methylation levels in PCa tissue and at least one non-tumor comparison tissue and/or studies reporting association between global methylation levels in PCa tissue and survival, disease recurrence or at least one clinicopathological prognostic factor. We summarized results using non-parametric comparisons and P-value summary methods.
We included 15 studies in the review: 6 studies with both diagnostic and prognostic information, 5 studies with only diagnostic information and 4 studies with only prognostic information. Quantitative meta-analysis was not possible because of the large heterogeneity in molecular techniques, types of tissues analyzed, aims and study designs. Summary statistical tests showed association of DNA hypomethylation with PCa diagnosis (P<0.006) and prognosis (P<0.001). Restriction to studies assessing 5-methylcytosine or long interspersed nucleotide element-1 revealed results in the same direction. Analyses restricted to specific clinicopathological features showed association with the presence of metastasis and tumor stage in all tests with P<0.03, and no association with Gleason score (all tests P>0.1 except for the weighted Z-test, P=0.05).
DNA hypomethylation was associated with PCa development and progression. However, due to the heterogeneity and small sample sizes of the included studies, along with the possibility of publication bias, this association requires additional assessment.
全基因组DNA甲基化在前列腺癌(PCa)中的作用仍不清楚。我们的目的是总结全基因组DNA低甲基化在PCa发生发展中的作用的相关证据。
我们检索了截至2013年12月的PubMed数据库,查找所有包含PCa组织和至少一种非肿瘤对照组织的全基因组甲基化水平信息的研究,以及/或者报告PCa组织全基因组甲基化水平与生存、疾病复发或至少一种临床病理预后因素之间关联的研究。我们使用非参数比较和P值汇总方法总结结果。
我们纳入了15项综述研究:6项研究同时包含诊断和预后信息,5项研究仅包含诊断信息,4项研究仅包含预后信息。由于分子技术、分析的组织类型、研究目的和研究设计存在很大异质性,无法进行定量荟萃分析。汇总统计检验显示DNA低甲基化与PCa诊断(P<0.006)和预后(P<0.001)相关。仅限于评估5-甲基胞嘧啶或长散在核苷酸元件-1的研究也得出了相同方向的结果。限于特定临床病理特征的分析显示,在所有检验中,DNA低甲基化与转移的存在和肿瘤分期相关(P<0.03),与Gleason评分无关联(除加权Z检验P=0.05外,所有检验P>0.1)。
DNA低甲基化与PCa的发生发展相关。然而,由于纳入研究的异质性、样本量小以及存在发表偏倚的可能性,这种关联需要进一步评估。