期刊
BIOMEDICINE & PHARMACOTHERAPY
卷 77, 期 -, 页码 1-6出版社
ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.biopha.2015.10.018
关键词
TGF-beta 1; Erlotinib; TKI resistance; NSCLC
资金
- National Natural Science Foundation of China [81101705, 81272532]
- Jiangsu Province Clinical Science and Technology Projects (Clinical Research Center) [BL2012008]
- Priority Academic Program Development of Jiangsu Higher Education Institutions [JX10231801]
- Natural Science Foundation of Jiangsu Province [BK2011852]
Background: TKI-acquired resistance is a tough obstacle for effectively treating NSCLC patients with EGFR mutant characteristics. T790M mutations and MET amplifications account for 70% of the acquired resistance, but the causes for the remaining 30% need elucidation. Methods: We detected TGF-beta 1 and PTEN expression levels in 51 NSCLC patients undergoing EGFR-TKI treatment using Immunohistochemistry (IHC) assay. We examined erlotinib sensitivity, apoptosis rate, and invasion ability in PC-9 cells and PC-9/TGF-beta 1 cells with CCK-8, flow cytometry, and trans-well assays. We examined and analyzed the AKT and ERK pathways' expression levels using western blot. Results: High TGF-beta 1 and low PTEN expression levels were correlated with poor EGFR-TKI sensitivity and overall survival in 51 NSCLC samples. In vitro analysis revealed that TGF-b1 could reduce erlotinib sensitivity, increase anti-apoptosis ability and invasive characteristic in TKI-sensitive PC-9 cell lines by down-regulating PTEN and activating the Akt and ERK pathways. Conclusions: The results suggest that TGF-beta 1 demonstrated another acquired erlotinib resistance by down-regulating PTEN expression. (C) 2015 Published by Elsevier Masson SAS.
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