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hTRT催化功能区基因克隆及其在肿瘤中的表达 被引量:18

Molecular cloning of hTRT catalytic domain and its expression in tumors
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摘要 目的研究端粒酶蛋白hTRT基因在肿瘤中的表达及其意义。方法用RTPCR法检测HeLa细胞与PG细胞的hTRT表达水平;将HeLa细胞的hTRT催化功能区克隆,并进行测序比较;应用原位杂交技术对肿瘤组织中的hTRT和hTR(端粒酶RNA组分)基因进行检测。结果HeLa细胞与PG细胞均有hTRT表达,HeLa细胞hTRT催化功能区cDNA序列与文献报道一致。原位杂交结果显示hTRT与hTR的协同表达率为926%(50/54例),hTRT和hTR在恶性肿瘤中的阳性率分别为826%(38/46例)870%(40/46例),hTRT和hTR在良性肿瘤中均呈阴性。结论HeLa细胞与PG细胞均有hTRT表达,hTRT的催化功能区具有高度保守性,hTRT与hTR在肿瘤中均为高表达,且hTRT与hTR有很大相关性(P<001),原位杂交技术检测hTR与hTRT对恶性肿瘤的诊断具有重要意义。 Objective To study the expression of hTRT gene in tumors and its significance in cancer diagnosis. Methods The expression of hTRT in HeLa cells and PG cells was estimated by RT PCR and the hTRT cDNA encoding the catalytic domain from HeLa cells were cloned and sequenced. Using in situ hybridization (ISH) techniques, the expression of hTRT mRNA in 54 human tumors were observed and compared with the expression of hTR. Results hTRT was detected in both HeLa and PG cells. Sequencing showed that the cloned hTRT catalytic domain cDNA was identical with that reported in the literature. hTRT and hTR expressions were detected in 38/46 and 40/46 malignant tumors respectively, while both hTRT and hTR were not detected in 8 benign tumors. Conclusion hTRT was detected in both HeLa and PG cancer cells. hTRT catalytic domains were highly conservative. The expression of hTRT and hTR were both high in malignant tumors and they were strongly correlated. Our results suggest that detection of hTRT was valuable to clinical oncology diagnosis.
出处 《中华病理学杂志》 CAS CSCD 北大核心 1999年第2期85-88,共4页 Chinese Journal of Pathology
关键词 端粒酶 原位杂交 基因表达 肿瘤 HTRT Telomerase In sita hybridzation Gene expression
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参考文献3

  • 1Beattie T L,Curr Biol,1998年,8卷,177页
  • 2Shang J W,Eur J Cancer,1997年,33卷,787页
  • 3Feng J,Science,1997年,269卷,1236页

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