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RASSF1A启动子甲基化与肺癌风险的关联:一项荟萃分析。

Association of RASSF1A promoter methylation with lung cancer risk: a meta-analysis.

作者信息

Huang Ying-Ze, Wu Wei, Wu Kun, Xu Xiao-Ning, Tang Wen-Ru

机构信息

Lab of Molecular Genetics of Aging and Tumor, Medical Faculty, Kunming University of Science and Technology, Kunming, Yunnan, China E-mail :

出版信息

Asian Pac J Cancer Prev. 2014;15(23):10325-8. doi: 10.7314/apjcp.2014.15.23.10325.

Abstract

RASSF1A, regarded as a candidate tumor suppressor, is frequently silenced and inactivated by methylation of its promoter region in many human tumors. However, the association between RASSF1A promoter methylation and lung cancer risk remains unclear. To provide a more reliable estimate we conducted a meta-analysis of cohort studies to evaluate the potential role of RASSF1A promoter methylation in lung carcinogenesis. Relevant studies were identified by searches of PubMed, Web of Science, ProQest and Medline databasesusing the following key words: 'lung cancer or lung neoplasm or lung carcinoma', 'RASSF1A methylation' or 'RASSF1A hypermethylation'. According to the selection standard, 15 articles were identified and analysised by STATA 12.0 software. Combined odds ratio (OR) and 95% confidence interval (CI) were used to assess the strength of the association between RASSF1A promoter methylation and lung cancer risk. A chi-square-based Q test and sensitivity analyses were performed to test between-study heterogeneity and the contributions of single studies to the final results, respectively. Funnel plots were carried out to evaluate publication bias. Overall, a significant relationship between RASSF1A promoter methylation and lung cancer risk (OR, 16.12; 95%CI, 11.40-22.81; p<0.001) with no between-study heterogeneity. In subgroup analyses, increased risk of RASSF1A methylation in cases than controls was found for the NSCLC group (OR, 13.66, 95%CI, 9.529- 19.57) and in the SCLC group (OR, 314.85, 95%CI, 48.93-2026.2).

摘要

RASSF1A被认为是一种候选肿瘤抑制因子,在许多人类肿瘤中,其启动子区域的甲基化经常使其沉默并失活。然而,RASSF1A启动子甲基化与肺癌风险之间的关联仍不清楚。为了提供更可靠的估计,我们进行了一项队列研究的荟萃分析,以评估RASSF1A启动子甲基化在肺癌发生中的潜在作用。通过搜索PubMed、Web of Science、ProQest和Medline数据库,使用以下关键词识别相关研究:“肺癌或肺肿瘤或肺癌”、“RASSF1A甲基化”或“RASSF1A高甲基化”。根据选择标准,确定了15篇文章,并使用STATA 12.0软件进行分析。合并比值比(OR)和95%置信区间(CI)用于评估RASSF1A启动子甲基化与肺癌风险之间关联的强度。分别进行基于卡方的Q检验和敏感性分析,以检验研究间异质性以及单个研究对最终结果的贡献。绘制漏斗图以评估发表偏倚。总体而言,RASSF1A启动子甲基化与肺癌风险之间存在显著关系(OR,16.12;95%CI,11.40 - 22.81;p<0.001),且无研究间异质性。在亚组分析中,非小细胞肺癌组(OR,13.66,95%CI,9.529 - 19.57)和小细胞肺癌组(OR,314.85,95%CI,48.93 - 2026.2)中,病例组RASSF1A甲基化风险高于对照组。

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