首页> 外文期刊>International Journal of Cancer =: Journal International du Cancer >Distinct profiles of TERT TERT promoter mutations and telomerase expression in head and neck cancer and cervical carcinoma
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Distinct profiles of TERT TERT promoter mutations and telomerase expression in head and neck cancer and cervical carcinoma

机译:表达头部和颈部癌症中的Tert Tert启动子突变和端粒酶表达的明显曲线

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Two recurrent mutations (–124 G??A and ?146 G??A) in the core promoter region of the human telomerase reverse transcriptase ( TERT ) gene create consensus binding sites for ETS transcription factors and cause increased TERT expression in several tumour types. We analyzed TERT promoter mutations and TERT mRNA levels in head and neck cancer, cervical carcinoma and cervical intraepithelial neoplasia (CIN) as well as in C‐4I, CaSki, HeLa and SiHa cervical cell lines. Nucleotide sequence analysis of TERT promoter region showed that 33.3% of oral squamous cell carcinoma (SCC) and 16.8% of cervical SCC harboured mutually exclusive G to A transitions at nucleotide position ?124 or ?146. TERT promoter was mutated at nucleotide ?146 (G??A) in SiHa cell line. Other nucleotide changes creating in some cases putative ETS binding sites were more frequent in oral SCC (26.7%) than in cervical carcinoma (4.8%). The frequency of mutations was independent of human papillomavirus (HPV) tumour status in both cervical and oral cancer. Expression of TERT gene was significantly higher in TERT promoter mutated (–124G??A or ?146G??A) cervical SCC compared to not mutated SCC irrespective of HPV16 E6 and E7 levels. Such hot spot changes were not detected in oropharyngeal SCC, cervical adenocarcinoma and CIN lesions. Our results suggest that TERT promoter mutations play a relevant role in oral SCC as well as in cervical SCC, besides the already known effect of HPV16 E6 protein on TERT expression.
机译:在人端粒酶逆转录酶(TERT)基因的核心启动子区域中,两个复发突变(-124g +&βa和Δαa)基因的核心启动子区域,为ETS转录因子产生共有结合位点并导致高速表达增加在几种肿瘤类型中。我们分析了头部和颈部癌症,宫颈癌和宫颈上皮内肿瘤(CIN)以及C-4I,Caski,Hela和Siha宫颈细胞系中的Tert启动子突变和Tert mRNA水平。 TERT启动子区域的核苷酸序列分析表明,33.3%的口腔鳞状细胞癌(SCC)和16.8%的宫颈SCC在核苷酸位置α1或α146时覆盖相互排他性的G至过渡。 Tert启动子在Siha细胞系中突变在核苷酸β146(g'&g''a)。在某些情况下,在某些情况下产生的其他核苷酸变化在口服SCC(26.7%)中的推定ETS结合位点比宫颈癌(4.8%)更频繁。突变的频率与宫颈和口腔癌中的人乳头瘤病毒(HPV)肿瘤状态无关。 TERT启动子突变的TERT基因的表达显着升高(-124g?a或β146g?a)宫颈SCC与不突变的SCC相比,无论HPV16 E6和E7水平如何。在口咽SCC,宫颈腺癌和CIN病变中未检测到这种热点变化。我们的研究结果表明,除了HPV16 E6蛋白对TERT表达的已知作用外,Tert启动子突变在口服SCC和宫颈SCC中发挥着相关的作用。

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