亚洲头颈癌的基因组状况:对 1016 个样本的综合荟萃分析

Srikanth S. Manda , Nafisa Arfa , Neha Sharma , Aparna R. Parikh , Thomas J. Roberts , Sewanti Limaye , Venkataraman Ramachandran , Kumar Prabhash , Moni A. Kuriakose , Prashant Kumar
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引用次数: 0

摘要

头颈部癌症(HNC)是一组发生在口腔、咽部和喉部粘膜的多种恶性肿瘤,受吸烟、饮酒和人类乳头瘤病毒(HPV)感染等因素的影响。本研究对包括印度、韩国、日本、中国、新加坡和沙特阿拉伯在内的亚洲队列中的 HNC 基因突变情况进行了全面的荟萃分析。该分析强调了受环境暴露、生活习惯和遗传倾向影响的独特遗传特征。值得注意的是,印度和中国队列中富含的 RAF 家族蛋白是 RAF 抑制剂(如维莫非尼)的潜在治疗靶点。此外,新加坡患者的MET等特定突变可通过克唑替尼等药物得到有效治疗,从而对HNSCC产生快速反应。吸烟者的 CASP8 和 FAT1 基因突变频率较高。包括RYR2和ANK2在内的新驱动基因在吸烟者中出现了显著的突变频率。RAS信号通路被确定为HNC的主要驱动基因,这与全球流行的PIK3CA/MTOR通路形成鲜明对比。这项研究还强调了印度和沙特队列中 HRAS 突变的高患病率。该研究强调,有必要获得特定地区的数据,以了解独特的分子差异并开发有效的疗法。NBEA和ANK2被鉴定为HNC潜在的新型驱动基因,这为针对亚洲HNC患者的遗传特征进行研究和有针对性的治疗干预开辟了新途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genomic landscape of head and neck cancer in Asia: A comprehensive meta-analysis of 1016 samples

Head and neck cancer (HNC) is a diverse group of malignancies arising in the mucosal linings of the oral cavity, pharynx, and larynx, influenced by factors such as tobacco use, alcohol consumption, and human papillomavirus (HPV) infection. This study conducts a comprehensive meta-analysis of the mutational landscape of HNC across Asian cohorts, encompassing India, Korea, Japan, China, Singapore, and Saudi Arabia. The analysis highlights distinct genetic profiles influenced by environmental exposures, lifestyle habits, and genetic predispositions. Notably, the RAF family proteins, enriched in both Indian and Chinese cohorts, present potential therapeutic targets for RAF inhibitors like Vemurafenib. Additionaly, specific mutations like MET in Singaporean patients can be effectively addressed with drugs like Crizotinib, leading to rapid responses in HNSCC. Smokers exhibited high frequencies of CASP8 and FAT1 mutations. Novel driver genes, including RYR2 and ANK2, emerged with significant mutational frequencies in smokers. The RAS signaling pathway was identified as a prominent driver in HNC, contrasting with the globally prevalent PIK3CA/MTOR pathway. This study also underscores the high prevalence of HRAS mutations in Indian and Saudi cohorts. The study emphasizes the necessity for region-specific data to understand the unique molecular differences and develop effective therapies. The identification of NBEA and ANK2 as potential novel driver genes in HNC highlights new avenues for research and targeted therapeutic interventions tailored to the genetic profiles of Asian HNC patients.

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