Changes of the Alternative Splicing Variants of Human Telomerase Reverse Transcriptase during Gastric Carcinogenesis

被引:14
作者
Xu, Jin-Heng [1 ]
Wang, Yu-Chuan [2 ]
Geng, Xin [1 ]
Li, Yan-Yun [1 ]
Zhang, Wei-Ming [1 ]
机构
[1] Tianjin Med Univ, Dept Biochem & Mol Biol, Tianjin, Peoples R China
[2] Tianjin Inst Ophthalmol, Tianjin, Peoples R China
基金
中国国家自然科学基金;
关键词
Alternative splicing; Precancerous lesion; Gastric cancer; Telomerase reverse transcriptase; CATALYTIC SUBUNIT; HTERT; EXPRESSION; ADENOCARCINOMA; CANCER; GENE; PATHOLOGY; DELETION; RECEPTOR;
D O I
10.1159/000178152
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Objective: We attempted to reveal the changes of the human telomerase reverse transcriptase (hTERT) alternative splicing pattern in gastric carcinogenesis. Methods: Three alternative splicing sites (alpha, beta, gamma) were selected and designed PCR primer. The expression of 8 hTERT alternative splicing variants (ASVs) in normal gastric mucosa, precancerous lesions and gastric cancer were detected by seminested RT-PCR. The expression of beta-site remaining ASV (beta(+) ASV) in specimens of precancerous lesions and specimens of gastric cancer was detected by SYBER Green real-time PCR. Results: The positive rate of alpha(+)beta(+)gamma(+) ASV was significantly higher in gastric cancer than in precancerous lesions and normal mucosa (94.7 vs. 40.0% and 0%, p < 0.05). The positive rates of other ASVs were not different among the 3 groups (p > 0.05). The positive rates of beta(+) ASVs (including alpha(+)beta(+)gamma(+) ASV, alpha-deletion ASV, gamma-deletion ASV, alpha gamma-deletion ASV) were 11.1% in normal mucosa, 40.0% in precancerous lesions and 94.7% in gastric cancer (p < 0.05). SYBR Green real-time RT-PCR showed that the expression level of beta(+) ASV was 6.99 times higher in gastric cancer than in precancerous lesions. Conclusion: hTERT alternative splicing pattern is different during gastric carcinogenesis. beta(+) ASV was widely expressed in gastric carcinogenesis and may provide some information for diagnosis of gastric cancer or precancerous lesions. Copyright (C) 2009 S. Karger AG, Basel
引用
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页码:23 / 29
页数:7
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