Telomere Dysfunction in Nonalcoholic Fatty Liver Disease and Cryptogenic Cirrhosis

端粒 非酒精性脂肪肝 肝硬化 端粒酶逆转录酶 端粒酶 肝细胞癌 生物 衰老 内科学 荧光原位杂交 脂肪肝 逆转录酶 实时聚合酶链反应 癌症研究 胃肠病学 内分泌学 病理 疾病 聚合酶链反应 医学 遗传学 基因 染色体
作者
Ido Laish,Batya Mannasse-Green,Ruth Hadary,Tal Biron‐Shental,Fred M. Konikoff,Aliza Amiel,Yona Kitay‐Cohen
标识
DOI:10.1159/000454654
摘要

Nonalcoholic fatty liver disease (NAFLD) and cryptogenic cirrhosis (CC) are considered preneoplastic conditions that might progress to hepatocellular carcinoma. We evaluated parameters of telomere dysfunction in these patient groups to study the correlation between telomere length and the progression of NAFLD. We analyzed peripheral lymphocytes from 22 patients with NAFLD, 20 patients with CC, and 20 healthy, age-matched controls. Telomere length was analyzed using quantitative fluorescence in situ hybridization, and cellular senescence was evaluated by the percentage of cells with senescence-associated heterochromatin foci. The expression of telomerase reverse transcriptase (hTERT) mRNA was measured using polymerase chain reaction, and telomere capture (TC) was assessed with 2 Cytocell probes, 15qter and 13qter. Shorter telomere length and increased cellular senescence was demonstrated in patients with NAFLD, compared to the CC patients and healthy controls. While hTERT mRNA was significantly decreased, TC was increased in CC patients, compared to the NAFLD group and healthy individuals. Thus, there is a correlation between hTERT mRNA expression and telomere length in patients with NAFLD, which might be related to associated metabolic disorders and the risk of malignant transformation. Patients with CC, on the contrary, elongate their telomeres through the TC mechanism.

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