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人端粒酶逆转录酶C250T启动子突变和端粒长度作为头颈癌患者癌症进展的分子标志物。

hTERT C250T promoter mutation and telomere length as a molecular markers of cancer progression in patients with head and neck cancer.

作者信息

Barczak Wojciech, Suchorska Wiktoria M, Sobecka Agnieszka, Bednarowicz Karolina, Machczynski Piotr, Golusinski Pawel, Rubis Blazej, Masternak Michal M, Golusinski Wojciech

机构信息

Department of Head and Neck Surgery, Poznan University of Medical Sciences, The Greater Poland Cancer Centre, Garbary, Poznan, Greater Poland Voivodeship 61‑866, Poland.

Radiobiology Lab, The Greater Poland Cancer Centre, Garbary, Poznan, Greater Poland Voivodeship 61‑866, Poland.

出版信息

Mol Med Rep. 2017 Jul;16(1):441-446. doi: 10.3892/mmr.2017.6590. Epub 2017 May 17.

Abstract

Squamous cell carcinoma of the head and neck (HNSCC) is the sixth leading cause of cancer worldwide, representing over half a million incidents every year. Cancer cells, including HNSCC, are characterized by increased telomerase activity. This enzymatic complex is active in ~90% of all cancer types and is responsible for the lengthening of telomeres. Highly recurrent point mutations in the human telomerase reverse transcriptase (hTERT) promoter have recently been reported in a number of human neoplasms. The aim of the present study was to analyze the prevalence of the hTERT promoter C250T mutation and telomere length in the blood leukocytes of 61 patients with HNSCC and 49 healthy individuals. Quantitative polymerase chain reaction identified the hTERT promoter mutation in 36% of patients with HNSCC. To the best of our knowledge this is first report indicating the presence of shorter telomeres in early stage tumors. In addition, the results suggest that the C250T hTERT promoter mutation and telomere length assessment may serve as important molecular markers of HNSCC progression.

摘要

头颈部鳞状细胞癌(HNSCC)是全球第六大癌症死因,每年发病超过50万例。包括HNSCC在内的癌细胞具有端粒酶活性增加的特征。这种酶复合物在所有癌症类型中约90%具有活性,负责端粒的延长。最近在一些人类肿瘤中报道了人类端粒酶逆转录酶(hTERT)启动子中高度复发的点突变。本研究的目的是分析61例HNSCC患者和49名健康个体血液白细胞中hTERT启动子C250T突变的发生率和端粒长度。定量聚合酶链反应在36%的HNSCC患者中检测到hTERT启动子突变。据我们所知,这是首次报告表明早期肿瘤中端粒较短。此外,结果表明C250T hTERT启动子突变和端粒长度评估可能作为HNSCC进展的重要分子标志物。

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