Cargando…

全基因组芯片筛查非小细胞肺癌组织多药耐药相关基因

BACKGROUND AND OBJECTIVE: The aim of this study is to screen for multi-drug resistance-related genes of human non-small cell lung cancer (NSCLC), and provide the evidences for drug-sensitive predicting genes of different NSCLC patients treated with chemotherapeutic drugs. METHODS: Sensitivity and in...

Descripción completa

Detalles Bibliográficos
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/PMC6000436/
https://www.ncbi.nlm.nih.gov/pubmed/20677558
http://dx.doi.org/10.3779/j.issn.1009-3419.2010.04.10
_version_ 1783331724574326784
collection PubMed
description BACKGROUND AND OBJECTIVE: The aim of this study is to screen for multi-drug resistance-related genes of human non-small cell lung cancer (NSCLC), and provide the evidences for drug-sensitive predicting genes of different NSCLC patients treated with chemotherapeutic drugs. METHODS: Sensitivity and inhibition ratio of five antitumor drugs (NVB, GEM, TAL, DOC, CDDP) on 75 fresh NSCLC samples from different individuals were studied by means of culturing primary tumor cells and MTT assay. After the five chemotherapeutic drugs were used, multi-drug resistance-related genes of NSCLC with cDNA microarry on the samples which were all high sensitive and those resistant were screened. RESULTS: cDNA microarray analysis screened out 212 genes, 168 of which were up-regulated while the other 44 were down-regulated in the group of highly sensitive compared with the group of resistance. CONCLUSION: The multi-drug resistance of NSCLC may be correlative with the 212 genes screened by cDNA microarray; the detailed mechanisms of the genes still need to be detected in the future.
format Online
Article
Text
id pubmed-6000436
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher 中国肺癌杂志编辑部
record_format MEDLINE/PubMed
spelling pubmed-60004362018-07-06 全基因组芯片筛查非小细胞肺癌组织多药耐药相关基因 Zhongguo Fei Ai Za Zhi 临床研究 BACKGROUND AND OBJECTIVE: The aim of this study is to screen for multi-drug resistance-related genes of human non-small cell lung cancer (NSCLC), and provide the evidences for drug-sensitive predicting genes of different NSCLC patients treated with chemotherapeutic drugs. METHODS: Sensitivity and inhibition ratio of five antitumor drugs (NVB, GEM, TAL, DOC, CDDP) on 75 fresh NSCLC samples from different individuals were studied by means of culturing primary tumor cells and MTT assay. After the five chemotherapeutic drugs were used, multi-drug resistance-related genes of NSCLC with cDNA microarry on the samples which were all high sensitive and those resistant were screened. RESULTS: cDNA microarray analysis screened out 212 genes, 168 of which were up-regulated while the other 44 were down-regulated in the group of highly sensitive compared with the group of resistance. CONCLUSION: The multi-drug resistance of NSCLC may be correlative with the 212 genes screened by cDNA microarray; the detailed mechanisms of the genes still need to be detected in the future. 中国肺癌杂志编辑部 2010-04-20 /pmc/articles/PMC6000436/ /pubmed/20677558 http://dx.doi.org/10.3779/j.issn.1009-3419.2010.04.10 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 临床研究
全基因组芯片筛查非小细胞肺癌组织多药耐药相关基因
title 全基因组芯片筛查非小细胞肺癌组织多药耐药相关基因
title_full 全基因组芯片筛查非小细胞肺癌组织多药耐药相关基因
title_fullStr 全基因组芯片筛查非小细胞肺癌组织多药耐药相关基因
title_full_unstemmed 全基因组芯片筛查非小细胞肺癌组织多药耐药相关基因
title_short 全基因组芯片筛查非小细胞肺癌组织多药耐药相关基因
title_sort 全基因组芯片筛查非小细胞肺癌组织多药耐药相关基因
topic 临床研究
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000436/
https://www.ncbi.nlm.nih.gov/pubmed/20677558
http://dx.doi.org/10.3779/j.issn.1009-3419.2010.04.10
work_keys_str_mv AT quánjīyīnzǔxīnpiànshāicháfēixiǎoxìbāofèiáizǔzhīduōyàonàiyàoxiāngguānjīyīn
AT quánjīyīnzǔxīnpiànshāicháfēixiǎoxìbāofèiáizǔzhīduōyàonàiyàoxiāngguānjīyīn
AT quánjīyīnzǔxīnpiànshāicháfēixiǎoxìbāofèiáizǔzhīduōyàonàiyàoxiāngguānjīyīn
AT quánjīyīnzǔxīnpiànshāicháfēixiǎoxìbāofèiáizǔzhīduōyàonàiyàoxiāngguānjīyīn