[HTML][HTML] Repurposing sertraline sensitizes non–small cell lung cancer cells to erlotinib by inducing autophagy

X Jiang, W Lu, X Shen, Q Wang, J Lv, M Liu, F Cheng… - JCI insight, 2018 - ncbi.nlm.nih.gov
Lung cancer patients treated with tyrosine kinase inhibitors (TKIs) often develop resistance.
More effective and safe therapeutic agents are urgently needed to overcome TKI resistance …

[HTML][HTML] Combining EGFR-TKI with SAHA overcomes EGFR-TKI-acquired resistance by reducing the protective autophagy in non-small cell lung cancer

P Cao, Y Li, R Shi, Y Yuan, H Gong, G Zhu… - Frontiers in …, 2022 - frontiersin.org
At present, lung cancer is the cancer with the highest mortality rate in the world. The
emergence of EGFR tyrosine kinase inhibitors (TKIs) has greatly improved the survival of …

[HTML][HTML] MERTK activation drives osimertinib resistance in EGFR-mutant non–small cell lung cancer

D Yan, JM Huelse, D Kireev, Z Tan… - The Journal of …, 2022 - Am Soc Clin Investig
JCI - MERTK activation drives osimertinib resistance in EGFR-mutant non–small cell lung
cancer Go to JCI Insight About Editors Consulting Editors For authors Publication ethics Alerts …

[HTML][HTML] YAP1 synergize with YY1 transcriptional co-repress DUSP1 to induce osimertinib resistant by activating the EGFR/MAPK pathway and abrogating autophagy …

Y Ning, H Zheng, Y Yang, H Zang, W Wang… - … Journal of Biological …, 2023 - ncbi.nlm.nih.gov
YAP1 is a well-known core effector of the Hippo pathway in tumors, but its potential role in
osimertinib resistance remained unexplored. Our study provides evidence that YAP1 acts as …

[HTML][HTML] The autophagy inhibitor chloroquine overcomes the innate resistance of wild-type EGFR non-small-cell lung cancer cells to erlotinib

Y Zou, YH Ling, J Sironi, EL Schwartz… - Journal of Thoracic …, 2013 - Elsevier
Introduction The epidermal growth factor receptor (EGFR) inhibitor erlotinib is much less
effective in non–small-cell lung cancer (NSCLC) tumors with wild-type EGFR, than in tumors …

Targeting AKR1B1 inhibits glutathione de novo synthesis to overcome acquired resistance to EGFR-targeted therapy in lung cancer

KR Zhang, YF Zhang, HM Lei, YB Tang… - Science translational …, 2021 - science.org
Acquired resistance represents a bottleneck to molecularly targeted therapies such as
epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) treatment in lung …

Targeting acetylcholine signaling modulates persistent drug tolerance in EGFR-mutant lung cancer and impedes tumor relapse

M Nie, N Chen, H Pang, T Jiang… - The Journal of …, 2022 - Am Soc Clin Investig
Although first-line epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI)
therapy is effective for treating EGFR-mutant non–small cell lung cancer (NSCLC), it is now …

EGFR tyrosine kinase inhibitors activate autophagy as a cytoprotective response in human lung cancer cells

W Han, H Pan, Y Chen, J Sun, Y Wang, J Li, W Ge… - PloS one, 2011 - journals.plos.org
Epidermal growth factor receptor tyrosine kinase inhibitors gefitinib and erlotinib have been
widely used in patients with non-small-cell lung cancer. Unfortunately, the efficacy of EGFR …

miR-147b-mediated TCA cycle dysfunction and pseudohypoxia initiate drug tolerance to EGFR inhibitors in lung adenocarcinoma

WC Zhang, JM Wells, KH Chow, H Huang, M Yuan… - Nature …, 2019 - nature.com
Drug tolerance is an acute defence response preceding a fully drug-resistant state and
tumour relapse; however, there are few therapeutic agents targeting drug tolerance in the …

Protective autophagy decreases osimertinib cytotoxicity through regulation of stem cell-like properties in lung cancer

L Li, Y Wang, L Jiao, C Lin, C Lu, K Zhang, C Hu, J Ye… - Cancer Letters, 2019 - Elsevier
Osimertinib, a third-generation epidermal growth factor receptor-tyrosine kinase inhibitor
(EGFR-TKI), shows great efficacy in EGFR-mutant non-small cell lung cancer (NSCLC); …