Suppr超能文献

口腔鳞状细胞癌中促凋亡基因的表观遗传下调。

Epigenetic downregulation of the proapoptotic gene in oral squamous cell carcinoma.

作者信息

Chen Ying-Ju, Liao Shin-Wei, Lai Yen-Ling, Li Yu-Fen, Lu Yin-Che, Tai Chien-Kuo

机构信息

Department of Biomedical Sciences, National Chung Cheng University, Chia‑Yi 62102, Taiwan, R.O.C.

Department of Public Health, China Medical University, Taichung 40402, Taiwan, R.O.C.

出版信息

Mol Med Rep. 2025 Mar;31(3). doi: 10.3892/mmr.2024.13421. Epub 2024 Dec 20.

Abstract

Homeobox A5 () has been identified as a tumor suppressor gene in breast cancers, but its role in oral squamous cell carcinoma (OSCC) has not been confirmed. The Illumina GoldenGate Assay for methylation identified that DNA methylation patterns differ between tumorous and normal tissues in the oral cavity and that is one of the genes that are hypermethylated in oral tumor tissues. The present study obtained more‑complete information on the methylation status of by using the Illumina Infinium MethylationEPIC BeadChip and bisulfite sequencing assays. The results indicated that hypermethylation has great potential as a biomarker for detecting OSCC. Comparing RNA expression between normal oral tissue and OSCC tissue samples indicated that its median level was 2.06‑fold higher in normal tissues that in OSCC tissues. Moreover, treatment using the demethylating agent 5‑aza‑2'‑deoxycytidine can upregulate expression in OSCC cell lines, verifying that the silencing of is primarily regulated by its hypermethylation. It was also found that upregulation of expression can not only increase OSCC cell death but that it can also enhance the therapeutic effect of cisplatin both and , suggesting that is an epigenetically downregulated proapoptotic gene in OSCC.

摘要

同源盒A5(HOXA5)已被确定为乳腺癌中的一种肿瘤抑制基因,但其在口腔鳞状细胞癌(OSCC)中的作用尚未得到证实。用于甲基化检测的Illumina GoldenGate分析法确定,口腔肿瘤组织和正常组织之间的DNA甲基化模式存在差异,且HOXA5是口腔肿瘤组织中发生高甲基化的基因之一。本研究通过使用Illumina Infinium MethylationEPIC BeadChip和亚硫酸氢盐测序分析法,获得了关于HOXA5甲基化状态更完整的信息。结果表明,HOXA5高甲基化作为检测OSCC的生物标志物具有很大潜力。比较正常口腔组织和OSCC组织样本中HOXA5的RNA表达情况,结果显示其在正常组织中的中位水平比OSCC组织中高2.06倍。此外,使用去甲基化剂5-氮杂-2'-脱氧胞苷进行治疗可上调OSCC细胞系中HOXA5的表达,证实HOXA5的沉默主要由其高甲基化调控。研究还发现,HOXA5表达上调不仅可以增加OSCC细胞死亡,而且还能增强顺铂在体内和体外的治疗效果,表明HOXA5是OSCC中一个表观遗传下调的促凋亡基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e068/11683450/013bdd7ff314/mmr-31-03-13421-g00.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