Classification of small molecule protein kinase inhibitors based upon the structures of their drug-enzyme complexes

R Roskoski Jr - Pharmacological research, 2016 - Elsevier
Because dysregulation and mutations of protein kinases play causal roles in human
disease, this family of enzymes has become one of the most important drug targets over the …

[HTML][HTML] The relationship between COPD and lung cancer

AL Durham, IM Adcock - Lung cancer, 2015 - Elsevier
Both COPD and lung cancer are major worldwide health concerns owing to cigarette
smoking, and represent a huge, worldwide, preventable disease burden. Whilst the majority …

EGFR exon 20 insertion mutations in advanced non-small-cell lung cancer: current status and perspectives

J Hou, H Li, S Ma, Z He, S Yang, L Hao, H Zhou… - Biomarker …, 2022 - Springer
Platinum-based chemotherapy was previously the first-choice treatment for lung cancer. The
discovery of epidermal growth factor receptor (EGFR) gene mutations and the development …

Stress-induced EGFR trafficking: mechanisms, functions, and therapeutic implications

X Tan, PF Lambert, AC Rapraeger, RA Anderson - Trends in cell biology, 2016 - cell.com
Epidermal growth factor receptor (EGFR) has fundamental roles in normal physiology and
cancer, making it a rational target for cancer therapy. Surprisingly, however, inhibitors that …

[PDF][PDF] Actionable activating oncogenic ERBB2/HER2 transmembrane and juxtamembrane domain mutations

KB Pahuja, TT Nguyen, BS Jaiswal, K Prabhash… - Cancer cell, 2018 - cell.com
Deregulated HER2 is a target of many approved cancer drugs. We analyzed 111,176 patient
tumors and identified recurrent mutations in HER2 transmembrane domain (TMD) and …

Dacomitinib: first global approval

M Shirley - Drugs, 2018 - Springer
Dacomitinib (Vizimpro®) is an orally administered, small-molecule irreversible inhibitor of
HER1 (EGFR), HER2 and HER4 that was developed by Pfizer Inc. for the treatment of solid …

Safety and tolerability of epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors in oncology

RR Shah, DR Shah - Drug safety, 2019 - Springer
Tyrosine kinase inhibitors (TKIs) that target epidermal growth factor receptor (EGFR) have
dramatically improved progression-free survival in non-small-cell lung cancer (NSCLC) …

Development of radiohalogenated osimertinib derivatives as imaging probes for companion diagnostics of osimertinib

K Mishiro, R Nishii, I Sawazaki, T Sofuku… - Journal of medicinal …, 2022 - ACS Publications
Osimertinib is an epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor
approved for treating non-small-cell lung cancer (NSCLC) with EGFR mutations. Genetic …

[HTML][HTML] Mutational profiling of colorectal cancers with microsatellite instability

EI Lin, LH Tseng, CD Gocke, S Reil, DT Le, NS Azad… - Oncotarget, 2015 - ncbi.nlm.nih.gov
Microsatellite instability (MSI) is caused by defective mismatch repair in 15–20% of
colorectal cancers (CRCs). Higher mutation loads in tumors with mismatch repair deficiency …

Multifactorial diseases of the heart, kidneys, lungs, and liver and incident cancer: epidemiology and shared mechanisms

C Shi, S de Wit, E Učambarlić… - Cancers, 2023 - mdpi.com
Simple Summary Multifactorial diseases are caused by a combination of genetic and
environmental factors and various risk factors that accumulate with age. Cardiovascular …