Protein tyrosine kinase inhibitor resistance in malignant tumors: molecular mechanisms and future perspective

Y Yang, S Li, Y Wang, Y Zhao, Q Li - Signal transduction and targeted …, 2022 - nature.com
Protein tyrosine kinases (PTKs) are a class of proteins with tyrosine kinase activity that
phosphorylate tyrosine residues of critical molecules in signaling pathways. Their basal …

[PDF][PDF] Acquired resistance to third-generation EGFR-TKIs and emerging next-generation EGFR inhibitors

X Du, B Yang, Q An, YG Assaraf, X Cao, J Xia - The Innovation, 2021 - cell.com
The discovery that mutations in the EGFR gene are detected in up to 50% of lung
adenocarcinoma patients, along with the development of highly efficacious epidermal …

Single-cell transcriptional changes associated with drug tolerance and response to combination therapies in cancer

AF Aissa, AB Islam, MM Ariss, CC Go, AE Rader… - Nature …, 2021 - nature.com
Tyrosine kinase inhibitors were found to be clinically effective for treatment of patients with
certain subsets of cancers carrying somatic mutations in receptor tyrosine kinases. However …

Coregulation of pathways in lung cancer patients with EGFR mutation: therapeutic opportunities

R Rosell, AF Cardona, O Arrieta, A Aguilar… - British Journal of …, 2021 - nature.com
Epidermal growth factor receptor (EGFR) mutations in lung adenocarcinoma are a frequent
class of driver mutations. Single EGFR tyrosine kinase inhibitor (TKI) provides substantial …

Targeting the ALK–CDK9-Tyr19 kinase cascade sensitizes ovarian and breast tumors to PARP inhibition via destabilization of the P-TEFb complex

YY Chu, MK Chen, Y Wei, HH Lee, W Xia, YN Wang… - Nature Cancer, 2022 - nature.com
Abstract Poly (ADP-ribose) polymerase (PARP) inhibitors have demonstrated promising
clinical activity in multiple cancers. However, resistance to PARP inhibitors remains a …

PKCα and PKCδ: friends and rivals

JD Black, T Affandi, AR Black, ME Reyland - Journal of Biological Chemistry, 2022 - ASBMB
PKC comprises a large family of serine/threonine kinases that share a requirement for
allosteric activation by lipids. While PKC isoforms have significant homology, functional …

Suppression of EGFR/PKC-δ/NF-κB signaling associated with imipramine-inhibited progression of non-small cell lung cancer

PF Yueh, YH Lee, IT Chiang, WT Chen, KL Lan… - Frontiers in …, 2021 - frontiersin.org
Background Anti-depressants have been reported to own anti-tumor potential types of
cancers; however, the role of imipramine in non-small cell lung cancer (NSCLC) has not …

Highly mimetic ex vivo lung‐cancer spheroid‐based physiological model for clinical precision therapeutics

MY Shie, HY Fang, KW Kan, CC Ho, CY Tu… - Advanced …, 2023 - Wiley Online Library
Lung cancer remains a major health problem despite the considerable research into
prevention and treatment methods. Through a deeper understanding of tumors, patient …

TGFβ2-mediated epithelial–mesenchymal transition and NF-κB pathway activation contribute to osimertinib resistance

X Jiang, Y Xu, L Yuan, L Zhang, M Huang… - Acta Pharmacologica …, 2021 - nature.com
Osimertinib (AZD9291) has been widely used for the treatment of EGFR mutant non-small
cell lung cancer. However, resistance to osimertinib is inevitable. In this study we elucidated …

Proteomics of resistance to Notch1 inhibition in acute lymphoblastic leukemia reveals targetable kinase signatures

G Franciosa, JGA Smits, S Minuzzo… - Nature …, 2021 - nature.com
Notch1 is a crucial oncogenic driver in T-cell acute lymphoblastic leukemia (T-ALL), making
it an attractive therapeutic target. However, the success of targeted therapy using γ …