The strange case of CDK4/6 inhibitors: mechanisms, resistance, and combination strategies
ES Knudsen, AK Witkiewicz - Trends in cancer, 2017 - cell.com
Inhibitors of cyclin-dependent kinases (CDKs) 4/6 have emerged as a powerful class of
agents with clinical activity in several malignancies. Targeting the cell cycle represents a …
agents with clinical activity in several malignancies. Targeting the cell cycle represents a …
Recent advances of highly selective CDK4/6 inhibitors in breast cancer
H Xu, S Yu, Q Liu, X Yuan, S Mani, RG Pestell… - Journal of hematology & …, 2017 - Springer
Uncontrolled cell division is the hallmark of cancers. Full understanding of cell cycle
regulation would contribute to promising cancer therapies. In particular, cyclin-dependent …
regulation would contribute to promising cancer therapies. In particular, cyclin-dependent …
CDK4/6 inhibitors impair recovery from cytotoxic chemotherapy in pancreatic adenocarcinoma
B Salvador-Barbero, M Álvarez-Fernández… - Cancer cell, 2020 - cell.com
Inhibition of the cell-cycle kinases CDK4 and CDK6 is now part of the standard treatment in
advanced breast cancer. CDK4/6 inhibitors, however, are not expected to cooperate with …
advanced breast cancer. CDK4/6 inhibitors, however, are not expected to cooperate with …
Integrated proteogenomic characterization of urothelial carcinoma of the bladder
N Xu, Z Yao, G Shang, D Ye, H Wang, H Zhang… - Journal of hematology & …, 2022 - Springer
Background Urothelial carcinoma (UC) is the most common pathological type of bladder
cancer, a malignant tumor. However, an integrated multi-omics analysis of the Chinese UC …
cancer, a malignant tumor. However, an integrated multi-omics analysis of the Chinese UC …
Targeting the Retinoblastoma/E2F repressive complex by CDK4/6 inhibitors amplifies oncolytic potency of an oncolytic adenovirus
J Koch, SJ Schober, SV Hindupur, C Schöning… - Nature …, 2022 - nature.com
Abstract CDK4/6 inhibitors (CDK4/6i) and oncolytic viruses are promising therapeutic agents
for the treatment of various cancers. As single agents, CDK4/6 inhibitors that are approved …
for the treatment of various cancers. As single agents, CDK4/6 inhibitors that are approved …
The renaissance of cyclin dependent kinase inhibitors
T Ettl, D Schulz, RJ Bauer - Cancers, 2022 - mdpi.com
Simple Summary This review provides an overview of the state of knowledge and general
understanding of CDK inhibitors currently under development or clinically approved, with a …
understanding of CDK inhibitors currently under development or clinically approved, with a …
Structure-guided design and development of cyclin-dependent kinase 4/6 inhibitors: a review on therapeutic implications
Abstract Cyclin-dependent kinase 6 (EC 2.7. 11.22) play significant roles in numerous
biological processes and triggers cell cycle events. CDK6 controlled the transcriptional …
biological processes and triggers cell cycle events. CDK6 controlled the transcriptional …
[HTML][HTML] The potent and selective cyclin-dependent kinases 4 and 6 inhibitor ribociclib (LEE011) is a versatile combination partner in preclinical cancer models
S Kim, R Tiedt, A Loo, T Horn, S Delach, S Kovats… - Oncotarget, 2018 - ncbi.nlm.nih.gov
Inhibition of cyclin-dependent kinases 4 and 6 (CDK4/6) is associated with robust antitumor
activity. Ribociclib (LEE011) is an orally bioavailable CDK4/6 inhibitor that is approved for …
activity. Ribociclib (LEE011) is an orally bioavailable CDK4/6 inhibitor that is approved for …
STAT3/5 inhibitors suppress proliferation in bladder cancer and enhance oncolytic adenovirus therapy
SV Hindupur, SC Schmid, JA Koch, A Youssef… - International Journal of …, 2020 - mdpi.com
The JAK-STAT signalling pathway regulates cellular processes like cell division, cell death
and immune regulation. Dysregulation has been identified in solid tumours and STAT3 …
and immune regulation. Dysregulation has been identified in solid tumours and STAT3 …
Abemaciclib is effective against pancreatic cancer cells and synergizes with HuR and YAP1 inhibition
T Dhir, CW Schultz, A Jain, SZ Brown, A Haber… - Molecular Cancer …, 2019 - AACR
Mutation or promoter hypermethylation of CDKN2A is found in over 90% of pancreatic ductal
adenocarcinomas (PDAC) and leads to loss of function of cell-cycle inhibitors p16 (INK4A) …
adenocarcinomas (PDAC) and leads to loss of function of cell-cycle inhibitors p16 (INK4A) …