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口腔癌中的 Ras 癌基因:过去 20 年的研究进展

Ras oncogenes in oral cancer: the past 20 years.

机构信息

Department of Molecular Cellular Oncology and Microbiology, Tokyo Medical and Dental University, Tokyo, Japan.

出版信息

Oral Oncol. 2012 May;48(5):383-92. doi: 10.1016/j.oraloncology.2011.12.006. Epub 2012 Jan 11.

Abstract

Oral squamous cell carcinoma (OSCC) of head and neck is associated with high morbidity and mortality in both Western and Asian countries. Several risk factors for the development of oral cancer are very well established, including tobacco chewing, betel quid, smoking, alcohol drinking and human papilloma virus (HPV) infection. Apart from these risk factors, many genetic factors such as oncogenes, tumor suppressor genes and regulatory genes are identified to involve in oral carcinogenesis with these risk factors dependent and independent manner. Ras is one of the most frequently genetically deregulated oncogene in oral cancer. In this review, we analyze the past 22years of literature on genetic alterations such as mutations and amplifications of the isoforms of the ras oncogene in oral cancer. Further, we addressed the isoform-specific role of the ras in oral carcinogenesis. We also discussed how targeting the Akt and MEK, downstream effectors of the PI3K/Akt and MAPK pathways, respectively, would probably pave the possible molecular therapeutic target for the ras driven tumorigenesis in oral cancer. Analysis of these ras isoforms may critically enlighten specific role of a particular ras isoform in oral carcinogenesis, enhance prognosis and pave the way for isoform-specific molecular targeted therapy in OSCC.

摘要

头颈部口腔鳞状细胞癌(OSCC)在西方国家和亚洲国家都与高发病率和死亡率相关。有几个口腔癌发生的风险因素已得到很好的确立,包括咀嚼烟草、嚼槟榔、吸烟、饮酒和人乳头瘤病毒(HPV)感染。除了这些风险因素外,许多遗传因素,如癌基因、肿瘤抑制基因和调节基因,已被确定与口腔癌发生有关,这些风险因素以依赖和独立的方式参与其中。Ras 是口腔癌中最常发生遗传失调的癌基因之一。在这篇综述中,我们分析了过去 22 年来有关口腔癌中 ras 癌基因的异构体突变和扩增等遗传改变的文献。此外,我们还探讨了 ras 在口腔癌发生中的亚型特异性作用。我们还讨论了如何针对 Akt 和 MEK,分别作为 PI3K/Akt 和 MAPK 通路的下游效应物,为口腔癌中 ras 驱动的肿瘤发生提供可能的分子治疗靶点。分析这些 ras 异构体可能会批判性地阐明特定 ras 异构体在口腔癌发生中的特定作用,增强预后,并为 OSCC 的异构体特异性分子靶向治疗铺平道路。

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