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 …
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 …
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
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 …
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 …
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 …
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 …
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 …
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
Lung cancer remains a major health problem despite the considerable research into
prevention and treatment methods. Through a deeper understanding of tumors, patient …
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 …
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 …
it an attractive therapeutic target. However, the success of targeted therapy using γ …