[TEIF蛋白在结直肠肿瘤中的表达及其与中心体异常的关系]。

Ying Gao, Bo Zhang
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引用次数: 7

摘要

背景与目的:本课题组最近发现的端粒酶转录元件相互作用因子(TEIF)基因是一类人端粒酶逆转录酶(hTERT)基因的转录因子,在多种肿瘤组织中表达。本研究旨在评价TEIF蛋白在人类结直肠肿瘤中的表达,并探讨其与中心体异常的关系。方法:采用免疫组化方法检测10例正常肠黏膜组织、30例结直肠癌和54例结直肠腺瘤组织中TEIF的表达。免疫荧光法检测γ -微管蛋白的表达。结果:免疫组化结果显示,正常组与各肿瘤组TEIF蛋白表达差异均有统计学意义(P0.05)。TEIF强阳性率(>或=++)在癌组明显高于腺瘤组和正常组(均P0.05)。免疫荧光结果显示,结直肠癌组中心体扩增阳性率明显高于正常组和腺瘤组(P0.05)。结论:TEIF蛋白及中心体扩增在结直肠肿瘤中普遍存在。TEIF的表达水平与肿瘤组织学分级及恶性程度有关。TEIF蛋白表达与中心体扩增呈高度正相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Expression of TEIF protein in colorectal tumors and its correlation with centrosome abnormality].

Background and objective: Telomerase transcriptional elements-interacting factor (TEIF) gene found recently by our research group is a transcription factor of a kind of human telomerase reverse transcriptase (hTERT) gene, and expresses in many kinds of tumor tissues. This study was to evaluate the expression of TEIF protein in human colorectal tumors and to explore its correlation with centrosome abnormality.

Methods: The expression of TEIF in 10 specimens of normal intestinal mucosa tissue, 30 specimens of colorectal cancer, and 54 specimens of colorectal adenoma was detected by immunohistochemistry. The expression of gamma-tubulin was detected by immunofluorescence.

Results: Immunohistochemistry results showed that the differences of TEIF protein expression between the normal group and each tumor groups were statistically significant (P<0.01), and the difference of TEIF protein expression between the malignant tumor group and the benign group was not significant (P>0.05). TEIF strong positive rate (> or =++) was significantly higher in the carcinoma group than in the adenoma group or normal group (all P<0.001); the differences of TEIF strong positive rate between Grade I adenoma and Grade II or III adenoma were statistically significant (P<0.05), and the difference of TEIF strong positive rate between Grade II adenoma and Grade III adenoma was not statistically significant (P>0.05). Immunofluorescence results showed that centrosome amplification-positive rate was significantly higher in the colorectal cancer group than in the normal group or the adenoma group (both P<0.01); the difference of the centrosome amplification positive rate between Grade I adenoma and Grade III adenoma was statistically significant (P<0.05), and the differences of the centrosome amplification positive rate between Grade II adenoma and Grade I or III adenoma were statistically significant (P>0.05).

Conclusions: TEIF protein and centrosome amplification is commonly found in colorectal tumors. The expression level of TEIF is related to tumor histological grade and malignant degree. TEIF protein expression and centrosome amplification showed a high degree of positive correlation.

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