[HTML][HTML] Targeting cyclin-dependent kinases in human cancers: from small molecules to peptide inhibitors

M Peyressatre, C Prével, M Pellerano, MC Morris - Cancers, 2015 - mdpi.com
Cyclin-dependent kinases (CDK/Cyclins) form a family of heterodimeric kinases that play
central roles in regulation of cell cycle progression, transcription and other major biological …

Molecular connections between cancer cell metabolism and the tumor microenvironment

CR Justus, EJ Sanderlin, LV Yang - International journal of molecular …, 2015 - mdpi.com
Cancer cells preferentially utilize glycolysis, instead of oxidative phosphorylation, for
metabolism even in the presence of oxygen. This phenomenon of aerobic glycolysis …

Chemically induced degradation of CDK9 by a proteolysis targeting chimera (PROTAC)

CM Robb, JI Contreras, S Kour, MA Taylor… - Chemical …, 2017 - pubs.rsc.org
Cyclin-dependent kinase 9 (CDK9), a member of the cyclin-dependent protein kinase (CDK)
family, is involved in transcriptional elongation of several target genes. CDK9 is ubiquitously …

Cyclin dependent kinase 9 inhibitors for cancer therapy: miniperspective

YA Sonawane, MA Taylor, JV Napoleon… - Journal of medicinal …, 2016 - ACS Publications
Cyclin dependent kinase (CDK) inhibitors have been the topic of intense research for nearly
2 decades due to their widely varied and critical functions within the cell. Recently CDK9 has …

The emerging role of cyclin-dependent kinases (CDKs) in pancreatic ductal adenocarcinoma

B García-Reyes, AL Kretz, JP Ruff… - International journal of …, 2018 - mdpi.com
The family of cyclin-dependent kinases (CDKs) has critical functions in cell cycle regulation
and controlling of transcriptional elongation. Moreover, dysregulated CDKs have been …

Mechanisms of the CDK4/6 inhibitor palbociclib (PD 0332991) and its future application in cancer treatment

M Liu, H Liu, J Chen - Oncology reports, 2018 - spandidos-publications.com
An uncontrolled cell cycle is an obvious marker of tumor cells. The G1‑S phase is an
important restriction point in the normal cell cycle, but in cancer cells the restriction function …

Discovery of 4-((7H-Pyrrolo[2,3-d]pyrimidin-4-yl)amino)-N-(4-((4-methylpiperazin-1-yl)methyl)phenyl)-1H-pyrazole-3-carboxamide (FN-1501), an FLT3- and CDK …

Y Wang, Y Zhi, Q **, S Lu, G Lin, H Yuan… - Journal of Medicinal …, 2018 - ACS Publications
A series of 1-H-pyrazole-3-carboxamide derivatives have been designed and synthesized
that exhibit excellent FLT3 and CDK inhibition and antiproliferative activities. A structure …

[HTML][HTML] Cyclin-dependent kinase inhibitors as marketed anticancer drugs: where are we now? A short survey

G Mariaule, P Belmont - Molecules, 2014 - mdpi.com
In the early 2000s, the anticancer drug imatinib (Glivec®) appeared on the market, exhibiting
a new mode of action by selective kinase inhibition. Consequently, kinases became a …

Neurophysiological and neuropathological characterization of new murine models of chemotherapy-induced chronic peripheral neuropathies

VA Carozzi, A Canta, N Oggioni, B Sala… - Experimental …, 2010 - Elsevier
Cisplatin, paclitaxel and bortezomib belong to some of the most effective families of
chemotherapy drugs for solid and haematological cancers. Epothilones represent a new …

[HTML][HTML] Insights on structural characteristics and ligand binding mechanisms of CDK2

Y Li, J Zhang, W Gao, L Zhang, Y Pan, S Zhang… - International journal of …, 2015 - mdpi.com
Cyclin-dependent kinase 2 (CDK2) is a crucial regulator of the eukaryotic cell cycle.
However it is well established that monomeric CDK2 lacks regulatory activity, which needs …