In vitro study on blocking mTOR signaling pathway in EGFR-TKI resistance NSCLC

被引:3
作者
Xiang, Xu-Dong [1 ]
Yu, Jing [2 ]
Li, Gao-Feng [1 ]
Xie, Lin [3 ]
Li, Heng [4 ]
机构
[1] Kunming Med Univ, Affiliated Hosp 3, Dept Thorac Surg, Kunming 650118, Peoples R China
[2] Kunming Med Univ, Affiliated Hosp 3, Dept Gynecol Oncol, Kunming 650118, Peoples R China
[3] Kunming Med Univ, Affiliated Hosp 3, Dept Med Oncol, Kunming 650118, Peoples R China
[4] Kunming Med Univ, Kunming 650118, Peoples R China
关键词
Everolimus; EGFR; mTOR; NSCLC; Targeted therapy; LUNG-CANCER; PTEN; TUMORIGENESIS; INHIBITORS; EXPRESSION; FEATURES; INSULIN; TARGET;
D O I
10.1016/S1995-7645(14)60063-8
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Objective: To investigate the effect and mechanism of inhibitor everolimus on EGFR-TKI resistance NSCLC. Methods: MTT assay was used to detect proliferation of human non small cell lung cancer cell line A549. Flow cytometry was used to detect the changes of apoptosis and cycle distribution in each group after 24 h and 48 h. RT-PCR was used to detect the changes of PTEN and 4EBPI expression levels after 48 h of monotherapy and combination therapy. Results: MTT assay showed that everolimus had dose dependent inhibition against growth of A549 cells. Flow cytometry showed when everolimus could induce apoptosis and induce G0/G1 phase cell cycle arrest, which was time dependent (P<0.05). RT-PCR showed everolimus could increase PTEN and 4EBP1 expression. Conclusions: mTOR inhibitor everolimus has an inhibitory effect on EGFR-TKI resistant NSCLC, which cannot reverse the resistance effect of EGFR-TKI resistant cell line A549. The relationship between EGFR/AKT signaling pathway and the mTOR signaling pathway and the mechanism in non small cell lung cancer need further study.
引用
收藏
页码:394 / 397
页数:4
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