Suppr超能文献

3p21.3 候选肿瘤抑制基因的筛选及口腔鳞状细胞癌基因启动子甲基化的研究。

Screening of candidate tumor-suppressor genes in 3p21.3 and investigation of the methylation of gene promoters in oral squamous cell carcinoma.

机构信息

Department of Stomatology, Second Xiangya Hospital, Central South University, Changsha, Hunan 410011, PR China.

出版信息

Oncol Rep. 2013 Mar;29(3):1175-82. doi: 10.3892/or.2012.2213. Epub 2012 Dec 28.

Abstract

Oral squamous cell carcinoma (OSCC) is the most common type of head and neck malignant tumor. however, its pathological mechanisms have not yet been elucidated. In the present study, we screened for candidate tumor-suppressor genes (TSGs) related to OSCC among 10 candidate genes located in 3p21.3, a region abundant with TSGs based on previous studies, using semi-quantitative reverse transcription PCR (RT-PCR). Three genes, GNAT1, SEMA3B and AXUD1, with low or no expression in OSCC tissues and the cell line TCA8113 were selected, and the promoter methylation status was further analyzed by methylation-specific PCR (MS-PCR). Hypermethylation in the promoter regions of SEMA3B was found in OSCC tissues, and a significant difference in the frequency of methylation of SEMA3B was observed between OSCC and non-cancerous tissues. Furthermore, TCA8113 cells treated with 5-Aza-Cdc started to re-express SEMA3B at a concentration of 5 µM or higher. Our study confirmed that three candidate TSGs with low expression may be involved in OSCC and that hypermethylation in promoter regions may contribute to the low expression of SEMA3B. These findings offer novel insights for clarifying the molecular mechanisms of tumorigenesis of OSCC as well as for aiding in its clinical diagnosis and therapeutic strategy.

摘要

口腔鳞状细胞癌 (OSCC) 是最常见的头颈部恶性肿瘤。然而,其病理机制尚未阐明。在本研究中,我们使用半定量逆转录聚合酶链反应 (RT-PCR) 筛选了位于富含肿瘤抑制基因 (TSG) 的 3p21.3 上的 10 个候选基因中的与 OSCC 相关的候选 TSG。三个基因 GNAT1、SEMA3B 和 AXUD1 在 OSCC 组织和 TCA8113 细胞系中表达水平较低或无表达,进一步通过甲基化特异性聚合酶链反应 (MS-PCR) 分析了其启动子甲基化状态。在 OSCC 组织中发现 SEMA3B 启动子区域发生高甲基化,并且在 OSCC 和非癌组织之间观察到 SEMA3B 甲基化频率存在显著差异。此外,浓度为 5μM 或更高的 5-Aza-Cdc 处理 TCA8113 细胞开始重新表达 SEMA3B。我们的研究证实,三个低表达的候选 TSG 可能参与 OSCC 的发生,并且启动子区域的高甲基化可能导致 SEMA3B 的低表达。这些发现为阐明 OSCC 肿瘤发生的分子机制以及辅助其临床诊断和治疗策略提供了新的见解。

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