[HTML][HTML] Combination erlotinib-cisplatin and Atg3-mediated autophagy in erlotinib resistant lung cancer

JG Lee, R Wu - PloS one, 2012 - journals.plos.org
Tyrosine kinase inhibitors such as erlotinib are commonly used as a therapeutic agent
against cancer due to its relatively low side-effect profile and, at times, greater efficacy …

Vorinostat synergizes with EGFR inhibitors in NSCLC cells by increasing ROS via up-regulation of the major mitochondrial porin VDAC1 and modulation of the c-Myc …

A Leone, MS Roca, C Ciardiello… - Free Radical Biology …, 2015 - Elsevier
In non-small-cell lung cancer (NSCLC) patients, the activation of alternative pathways
contributes to the limited efficacy of the epidermal growth factor receptor (EGFR) tyrosine …

[HTML][HTML] Costunolide is a dual inhibitor of MEK1 and AKT1/2 that overcomes osimertinib resistance in lung cancer

X Tian, R Wang, T Gu, F Ma, KV Laster, X Li, K Liu… - Molecular Cancer, 2022 - Springer
EGFR-TKI targeted therapy is one of the most effective treatments for lung cancer patients
harboring EGFR activating mutations. However, inhibition response is easily attenuated by …

20 (S)-ginsenoside Rg3 sensitizes human non-small cell lung cancer cells to icotinib through inhibition of autophagy

XJ Wang, RJ Zhou, N Zhang, Z Jing - European journal of pharmacology, 2019 - Elsevier
Epidermal growth factor receptor tyrosine kinase inhibitors (EGFR–TKIs) have become a
standard therapy for non-small cell lung cancer (NSCLC) patients with sensitive mutations …

[HTML][HTML] Autophagic degradation of epidermal growth factor receptor in gefitinib-resistant lung cancer by celastrol

SW Xu, BYK Law, SWF Mok… - International …, 2016 - spandidos-publications.com
Drug resistance of non-small cell lung cancer (NSCLC) is highly correlated to the mutation of
the epidermal growth factor receptor (EGFR). Although EGFR tyrosine kinase inhibitors …

[HTML][HTML] Transcriptome profiling of acquired gefitinib resistant lung cancer cells reveals dramatically changed transcription programs and new treatment targets

N Wei, Y Song, F Zhang, Z Sun, X Zhang - Frontiers in Oncology, 2020 - frontiersin.org
Background: Targeted therapy for lung cancer with epidermal growth factor receptor (EGFR)
mutations with tyrosine kinase inhibitors (TKIs) represents one of the major breakthroughs in …

[HTML][HTML] JAK2 inhibitor TG101348 overcomes erlotinib-resistance in non-small cell lung carcinoma cells with mutated EGF receptor

F Zhang, W Yang, S Duan, Y Xia, R Zhu, Y Chen - Oncotarget, 2015 - ncbi.nlm.nih.gov
Non-small cell lung cancer (NSCLC) patients with epidermal growth factor receptor (EGFR)
mutations are responsive to EGFR-tyrosine kinase inhibitor (EGFR-TKI). However, NSCLC …

[HTML][HTML] The pan-HDAC inhibitor panobinostat acts as a sensitizer for erlotinib activity in EGFR-mutated and -wildtype non-small cell lung cancer cells

G Greve, I Schiffmann, D Pfeifer, M Pantic, J Schüler… - BMC cancer, 2015 - Springer
Background The receptor tyrosine kinase (RTK) EGFR is overexpressed and mutated in
NSCLC. These mutations can be targeted by RTK inhibitors (TKIs) such as erlotinib …

P21-activated kinase 2-mediated β-catenin signaling promotes cancer stemness and osimertinib resistance in EGFR-mutant non-small-cell lung cancer

Y Yi, P Li, Y Huang, D Chen, S Fan, J Wang, M Yang… - Oncogene, 2022 - nature.com
Osimertinib (AZD9291) is a third-generation epidermal growth factor receptor (EGFR)
tyrosine kinase inhibitor (TKI), used for treating patients with advanced non-small-cell lung …

[HTML][HTML] Cotargeting EGFR and autophagy signaling: A novel therapeutic strategy for non‑small‑cell lung cancer

X Sui, N Kong, M Zhu, X Wang… - Molecular and …, 2014 - spandidos-publications.com
Abstract epidermal growth factor receptor (EGFR) somatic mutations are found in the
majority of non‑small‑cell lung cancers (NSCLCs) and patients with NSCLC who harbor …