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实时荧光定量PCR检测人肺腺癌细胞Anip973、Anip973/NVB中hTERT mRNA的表达

BACKGROUND AND OBJECTIVE: Human telomerase reverse transcriptase is the catalytic subunit of telomerase, and its activity is correlated with cell's sensitivity to chemotherapy. The aim of this study is to investigate the differential expression of human telomerase reverse transcriptase (hTERT)...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000433/
https://www.ncbi.nlm.nih.gov/pubmed/20677553
http://dx.doi.org/10.3779/j.issn.1009-3419.2010.04.05
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collection PubMed
description BACKGROUND AND OBJECTIVE: Human telomerase reverse transcriptase is the catalytic subunit of telomerase, and its activity is correlated with cell's sensitivity to chemotherapy. The aim of this study is to investigate the differential expression of human telomerase reverse transcriptase (hTERT) mRNA in human lung adenocarcinoma cell line Anip973 and Anip973/NVB, and to observe the correlation between hTERT mRNA and drug-resistance. METHODS: The real-time fluorescence quantitative RT-PCR was used to detect the change of hTERT mRNA in human lung adenocarcinoma drug-resistant cell Anip973/NVB and parental cell Anip973 treated by NVB. RESULTS: In the control group, the expression of hTERT mRNA showed no significant difference between drug-resistant cell Anip973/NVB and parental cell Anip973. After been treated by NVB, the expression of hTERT mRNA in parental cell was significantly decreased (P < 0.01), and drug-resistant cell Anip973/ NVB had no evidently variant (P > 0.05). The down-regulated hTERT mRNA in Anip973 cell was higher than that in Anip973/ NVB cell. CONCLUSION: Telomerase correlates with the drug-resistant cell A973/NVB, and telomerase may be a new target for multi-drug resistant inversion.
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spelling pubmed-60004332018-07-06 实时荧光定量PCR检测人肺腺癌细胞Anip973、Anip973/NVB中hTERT mRNA的表达 Zhongguo Fei Ai Za Zhi 基础研究 BACKGROUND AND OBJECTIVE: Human telomerase reverse transcriptase is the catalytic subunit of telomerase, and its activity is correlated with cell's sensitivity to chemotherapy. The aim of this study is to investigate the differential expression of human telomerase reverse transcriptase (hTERT) mRNA in human lung adenocarcinoma cell line Anip973 and Anip973/NVB, and to observe the correlation between hTERT mRNA and drug-resistance. METHODS: The real-time fluorescence quantitative RT-PCR was used to detect the change of hTERT mRNA in human lung adenocarcinoma drug-resistant cell Anip973/NVB and parental cell Anip973 treated by NVB. RESULTS: In the control group, the expression of hTERT mRNA showed no significant difference between drug-resistant cell Anip973/NVB and parental cell Anip973. After been treated by NVB, the expression of hTERT mRNA in parental cell was significantly decreased (P < 0.01), and drug-resistant cell Anip973/ NVB had no evidently variant (P > 0.05). The down-regulated hTERT mRNA in Anip973 cell was higher than that in Anip973/ NVB cell. CONCLUSION: Telomerase correlates with the drug-resistant cell A973/NVB, and telomerase may be a new target for multi-drug resistant inversion. 中国肺癌杂志编辑部 2010-04-20 /pmc/articles/PMC6000433/ /pubmed/20677553 http://dx.doi.org/10.3779/j.issn.1009-3419.2010.04.05 Text en 版权所有©《中国肺癌杂志》编辑部2010 https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) License. See: https://creativecommons.org/licenses/by/3.0/
spellingShingle 基础研究
实时荧光定量PCR检测人肺腺癌细胞Anip973、Anip973/NVB中hTERT mRNA的表达
title 实时荧光定量PCR检测人肺腺癌细胞Anip973、Anip973/NVB中hTERT mRNA的表达
title_full 实时荧光定量PCR检测人肺腺癌细胞Anip973、Anip973/NVB中hTERT mRNA的表达
title_fullStr 实时荧光定量PCR检测人肺腺癌细胞Anip973、Anip973/NVB中hTERT mRNA的表达
title_full_unstemmed 实时荧光定量PCR检测人肺腺癌细胞Anip973、Anip973/NVB中hTERT mRNA的表达
title_short 实时荧光定量PCR检测人肺腺癌细胞Anip973、Anip973/NVB中hTERT mRNA的表达
title_sort 实时荧光定量pcr检测人肺腺癌细胞anip973、anip973/nvb中htert mrna的表达
topic 基础研究
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000433/
https://www.ncbi.nlm.nih.gov/pubmed/20677553
http://dx.doi.org/10.3779/j.issn.1009-3419.2010.04.05
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