Suppr超能文献

肝细胞癌中PDCD4基因的高甲基化与表达沉默:一项联合研究

Hypermethylation and Expression Silencing of PDCD4 Gene in Hepatocellular Carcinoma: A Consort Study.

作者信息

Ding Xianglian, Cheng Xifang, Gong Meixia, Chen Xiaojun, Yin Fang, Lai Kailan

机构信息

From the Department of Radiology, The 5th Affiliated Hospital of Sun Yat-Sen University, Zhuhai, China.

出版信息

Medicine (Baltimore). 2016 Feb;95(6):e2729. doi: 10.1097/MD.0000000000002729.

Abstract

Programmed cell death 4 (PDCD4) is a novel tumor suppressor, which is involved in the initiation and progression of cancers. However, the role of PDCD4 in hepatocellular carcinoma (HCC) has not been reported. The aim of this study was to investigate the molecular mechanism and clinical significance of PDCD4 inactivation in HCC.The mRNA levels of PDCD4 in HCC tissues and adjacent nontumor tissues were analyzed by quantitative real-time polymerase chain reaction (qRT-PCR). Bisulfite sequencing PCR was performed to determine the methylation status of PDCD4 promoter. Furthermore, the mRNA expression level and the methylated level of PDCD4 were analyzed with the clinical and pathological characteristics.qRT-PCR analysis showed that PDCD4 mRNA levels in tumor tissues were significantly decreased compared with that in adjacent nontumor tissues. The methylation rate of PDCD4 promoter was significantly higher in HCC tissues than that in adjacent nontumor tissues. PDCD4 mRNA levels and promoter methylation levels were both statistically correlated with metastasis and the degree of differentiation in HCC. In addition, the correlation between PDCD4 hypermethylation, mRNA levels, and overall survival (OS) was statistically significant.Our results indicated that PDCD4 may be a novel candidate of tumor suppressor gene in HCC, and that promoter hypermethylation is an important mechanism for its downregulation and is also a good predictor of OS for HCC.

摘要

程序性细胞死亡4(PDCD4)是一种新型肿瘤抑制因子,参与癌症的发生和发展。然而,PDCD4在肝细胞癌(HCC)中的作用尚未见报道。本研究旨在探讨HCC中PDCD4失活的分子机制及临床意义。通过定量实时聚合酶链反应(qRT-PCR)分析HCC组织和癌旁非肿瘤组织中PDCD4的mRNA水平。采用亚硫酸氢盐测序PCR法检测PDCD4启动子的甲基化状态。此外,分析了PDCD4的mRNA表达水平和甲基化水平与临床病理特征的关系。qRT-PCR分析显示,肿瘤组织中PDCD4的mRNA水平显著低于癌旁非肿瘤组织。HCC组织中PDCD4启动子的甲基化率显著高于癌旁非肿瘤组织。PDCD4的mRNA水平和启动子甲基化水平均与HCC的转移和分化程度具有统计学相关性。此外,PDCD4高甲基化、mRNA水平与总生存期(OS)之间的相关性具有统计学意义。我们的结果表明,PDCD4可能是HCC中一种新型的肿瘤抑制基因候选者,启动子高甲基化是其下调的重要机制,也是HCC患者OS的良好预测指标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fcc/4753909/4e20b394a79e/medi-95-e2729-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验