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喉癌中癌症1中高甲基化的肿瘤抑制基因的表达。

Expression of the tumor suppressor gene hypermethylated in cancer 1 in laryngeal carcinoma.

作者信息

Markowski Jarosław, Sieroń Aleksander L, Kasperczyk Katarzyna, Ciupińska-Kajor Monika, Auguściak-Duma Aleksandra, Likus Wirginia

机构信息

Department of Laryngology, School of Medicine in Katowice, Medical University of Silesia, Katowice 40-027, Poland.

Department of Molecular Biology and Genetics, School of Medicine in Katowice, Medical University of Silesia, Katowice 40-752, Poland ; CoE Research and Teaching of Molecular Biology of Matrix and Nanotechnology, Network of CoE BioMedTech Silesia, Katowice 40-752, Poland.

出版信息

Oncol Lett. 2015 May;9(5):2299-2302. doi: 10.3892/ol.2015.2983. Epub 2015 Feb 25.

Abstract

Hypermethylated in cancer 1 (HIC1) is a putative suppressor gene, cooperating with TP53 in the regulation of apoptosis. The promoter site of this gene contains CpG islands susceptible to methylation. Altered methylation leads to the silencing of HIC1. Persistent loss of HIC1 function reflects the attenuation of proapoptotic characteristics of TP53 and may constitute the background for carcinogenesis. Altered methylation profiles along with diminished expression of HIC1 were documented in a number of solid neoplasms. The aim of this study was to evaluate the expression of the HIC1 gene in laryngeal carcinoma. RNA was extracted from samples of laryngeal cancer and corresponding healthy tissues of 21 patients with advanced laryngeal cancer (T3-T4). The amount of RNA (cDNA) was evaluated using reverse transcription-quantitative polymerase chain reaction with GADPH as the reference gene. Data demonstrated that HIC1 expression was significantly reduced in laryngeal cancer tissues. The relative expression of HIC1 was found to be ~40% lower in tumor samples compared to that in healthy controls. The median tumor/normal tissue ratio for HIC1 was 0.615. These results suggest that low HIC1 expression may be associated with neoplastic transformation in the larynx.

摘要

癌症高甲基化1(HIC1)是一种假定的抑癌基因,在细胞凋亡调控中与TP53协同作用。该基因的启动子区域含有易发生甲基化的CpG岛。甲基化改变导致HIC1沉默。HIC1功能的持续丧失反映了TP53促凋亡特性的减弱,可能构成致癌作用的背景。在许多实体瘤中都记录到甲基化谱改变以及HIC1表达降低。本研究的目的是评估HIC1基因在喉癌中的表达。从21例晚期喉癌(T3 - T4)患者的喉癌样本及相应健康组织中提取RNA。以GADPH作为参照基因,采用逆转录定量聚合酶链反应评估RNA(cDNA)量。数据表明,喉癌组织中HIC1表达显著降低。与健康对照相比,肿瘤样本中HIC1的相对表达量低约40%。HIC1的肿瘤/正常组织中位比值为0.615。这些结果表明,HIC1低表达可能与喉的肿瘤转化有关。

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