Open AccessIncreased expression of miR‐641 contributes to erlotinib resistance in non‐small‐cell lung cancer cells by targeting NF 1
Author(s) -
Chen Juan,
Cui Jieda,
Guo Xiaotong,
Cao Xia,
Li Qing
Publication year - 2018
Publication title -
cancer medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.403
H-Index - 53
ISSN - 2045-7634
DOI - 10.1002/cam4.1326
Subject(s) - erlotinib , cancer research , lung cancer , gefitinib , epidermal growth factor receptor , medicine , apoptosis , mapk/erk pathway , tyrosine kinase , erlotinib hydrochloride , gene silencing , cell growth , signal transduction , cancer , oncology , biology , receptor , microbiology and biotechnology , biochemistry , gene , genetics
Epidermal growth receptor ( EGFR )‐targeted tyrosine kinase inhibitors ( TKI s) have emerged as first‐line drugs for advanced non‐small‐cell lung cancer ( NSCLC ) patients with EFGR mutations. However, most patients with NSCLC show acquired resistance to EGFR ‐ TKI s, and low expression of NF 1 is a mechanism of EGFR ‐ TKI resistance in lung cancer. However, the mechanism by which NF 1 is downregulated in EGFR ‐ TKI ‐resistant NSCLC is unclear. Here, we found the increased expression of miR‐641 in NSCLC cells and human NSCLC samples with resistance to TKI compared to those with sensitive to TKI . In addition, our in vitro experiments show that overexpression of miR‐641 induces TKI resistance in NSCLC cells. Furthermore, we identified that miR‐641 activates ERK signaling by direct targeting of neurofibromatosis 1 ( NF 1) in NSCLC cells. Our data show that overexpression of NF 1 or silencing of ERK can block miR‐641‐induced resistance of NSCLC cells to erlotinib treatment. Importantly, our animal experiments show that combination of miR‐641 inhibition and erlotinib treatment can significantly inhibit erlotinib‐resistant NSCLC growth, inhibit proliferation and induce apoptosis compared to single‐drug treatment. Our findings suggest that increased expression of miR‐641 significantly contributes to erlotinib resistance development in NSCLC cells through activating ERK signaling by targeting NF 1 and that inhibition of miR‐641 may reverse acquired resistance of NSCLC cells to erlotinib treatment.