[HTML][HTML] Relevance of genetic alterations in squamous and small cell lung cancer

JK Sabari, PK Paik - Annals of Translational Medicine, 2017 - ncbi.nlm.nih.gov
The precision medicine revolution has led to the development and US FDA approval of
multiple targeted therapies in non-squamous non-small cell lung cancers, including tyrosine …

NCAPG2 Maintains Cancer Stemness and Promotes Erlotinib Resistance in Lung Adenocarcinoma

S Jiang, J Huang, H He, Y Liu, L Liang, X Sun, Y Li… - Cancers, 2022 - mdpi.com
Simple Summary This study investigated the relationship between erlotinib resistance and
stemness in lung adenocarcinoma. NCAPG2 was identified as an erlotinib resistance gene …

Acquired BRAF rearrangements induce secondary resistance to EGFR therapy in EGFR-mutated lung cancers

M Vojnic, D Kubota, C Kurzatkowski, M Offin… - Journal of Thoracic …, 2019 - Elsevier
Introduction Multiple genetic mechanisms have been identified in EGFR-mutant lung
cancers as mediators of acquired resistance (AR) to EGFR tyrosine kinase inhibitors (TKIs) …

[HTML][HTML] Acquired nintedanib resistance in FGFR1-driven small cell lung cancer: role of endothelin-A receptor-activated ABCB1 expression

B Englinger, D Loetsch, C Pirker, T Mohr… - Oncotarget, 2016 - ncbi.nlm.nih.gov
Genomically amplified fibroblast growth factor receptor 1 (FGFR1) is an oncogenic driver in
defined lung cancer subgroups and predicts sensibility against FGFR1 inhibitors in this …

[HTML][HTML] Paradoxical functions of ZEB1 in EGFR-mutant lung cancer: tumor suppressor and driver of therapeutic resistance

ZA Yochum, MA Socinski, TF Burns - Journal of Thoracic Disease, 2016 - ncbi.nlm.nih.gov
© Journal of Thoracic Disease. All rights reserved. J Thorac Dis 2016; 8 (11): E1528-E1531
jtd. amegroups. com other miR-200c targets and potentially other ZEB1 target genes or …

Combined EGFR/MEK Inhibition Prevents the Emergence of Resistance in EGFR-Mutant Lung Cancer

EM Tricker, C Xu, S Uddin, M Capelletti, D Ercan… - Cancer discovery, 2015 - AACR
Irreversible pyrimidine-based EGFR inhibitors, including WZ4002, selectively inhibit both
EGFR-activating and EGFR inhibitor–resistant T790M mutations more potently than wild …

Acquired resistance to KRAS G12C small-molecule inhibitors via genetic/nongenetic mechanisms in lung cancer

A Mohanty, A Nam, S Srivastava, J Jones… - Science …, 2023 - science.org
Inherent or acquired resistance to sotorasib poses a substantialt challenge for NSCLC
treatment. Here, we demonstrate that acquired resistance to sotorasib in isogenic cells …

Understanding Lineage Plasticity as a Path to Targeted Therapy Failure in EGFR-Mutant Non-small Cell Lung Cancer

T Shaurova, L Zhang, DW Goodrich… - Frontiers in …, 2020 - frontiersin.org
Somatic alterations in the epidermal growth factor receptor gene (EGFR) result in aberrant
activation of kinase signaling and occur in∼ 15% of non-small cell lung cancers (NSCLC) …

[HTML][HTML] FGFR1 activation is an escape mechanism in human lung cancer cells resistant to afatinib, a pan-EGFR family kinase inhibitor

K Azuma, A Kawahara, K Sonoda, K Nakashima… - Oncotarget, 2014 - ncbi.nlm.nih.gov
Most NSCLC patients with EGFR mutations benefit from treatment with EGFR-TKIs, but the
clinical efficacy of EGFR-TKIs is limited by the appearance of drug resistance. Multiple …

Bruceine H mediates EGFR-TKI drug persistence in NSCLC by notch3-dependent β-catenin activating FOXO3a signaling

J Wu, X He, Z Xiong, L Shi, D Chen, Y Feng… - Frontiers in …, 2022 - frontiersin.org
Tyrosine kinase inhibitors (TKIs) targeting epidermal growth factor receptor (EGFR) protein
serve as a critical pillar in the treatment of non-small cell lung cancer (NSCLC), but …