[HTML][HTML] Therapeutic potential of flavonoids in cancer: ROS-mediated mechanisms

H Slika, H Mansour, N Wehbe, SA Nasser… - Biomedicine & …, 2022 - Elsevier
Cancer is a leading cause of morbidity and mortality around the globe. Reactive oxygen
species (ROS) play contradicting roles in cancer incidence and progression. Antioxidants …

Inhibitors of cyclin-dependent kinases as cancer therapeutics

SR Whittaker, A Mallinger, P Workman… - Pharmacology & …, 2017 - Elsevier
Over the past two decades there has been a great deal of interest in the development of
inhibitors of the cyclin-dependent kinases (CDKs). This attention initially stemmed from …

Cyclin-dependent kinase pathways as targets for cancer treatment

GI Shapiro - Journal of clinical oncology, 2006 - ascopubs.org
Cyclin-dependent kinases (cdks) are critical regulators of cell cycle progression and RNA
transcription. A variety of genetic and epigenetic events cause universal overactivity of the …

Targeting the cell cycle: a new approach to cancer therapy

GK Schwartz, MA Shah - Journal of clinical oncology, 2005 - ascopubs.org
The cell cycle represents a series of tightly integrated events that allow the cell to grow and
proliferate. Critical parts of the cell cycle machinery are the cyclin-dependent kinases …

Phase II trial of veliparib in patients with previously treated BRCA-mutated pancreas ductal adenocarcinoma

MA Lowery, DP Kelsen, M Capanu, SC Smith… - European Journal of …, 2018 - Elsevier
Purpose BRCA-associated cancers have increased sensitivity to poly (ADP-ribose)
polymerase inhibitors (PARPis). This single arm, non-randomised, multicentre phase II trial …

The CDK inhibitors in cancer research and therapy

J Cicenas, M Valius - Journal of cancer research and clinical oncology, 2011 - Springer
Chemical compounds that interfere with an enzymatic function of kinases are useful for
gaining insight into the complicated biochemical processes in mammalian cells. Cyclin …

Flavopiridol administered using a pharmacologically derived schedule is associated with marked clinical efficacy in refractory, genetically high-risk chronic …

JC Byrd, TS Lin, JT Dalton, D Wu, MA Phelps, B Fischer… - Blood, 2007 - ashpublications.org
Despite promising preclinical studies with the cyclin-dependent kinase inhibitor flavopiridol
in chronic lymphocytic leukemia (CLL) and other diseases, previous clinical trials with this …

CAK—cyclin-dependent activating kinase: a key kinase in cell cycle control and a target for drugs?

G Lolli, LN Johnson - Cell cycle, 2005 - Taylor & Francis
The Cyclin-dependent kinase (CDK) Activating Kinase (CAK) is responsible for the
activating phosphorylation of CDK1, CDK2, CDK4 and CDK6 and regulation of the cell …

Phase II study of flavopiridol in relapsed chronic lymphocytic leukemia demonstrating high response rates in genetically high-risk disease

TS Lin, AS Ruppert, AJ Johnson, B Fischer… - Journal of Clinical …, 2009 - ascopubs.org
Purpose Patients with chronic lymphocytic leukemia (CLL) with high-risk genomic features
achieve poor outcomes with traditional therapies. A phase I study of a pharmacokinetically …

Clinical potential of novel therapeutic targets in breast cancer: CDK4/6, Src, JAK/STAT, PARP, HDAC, and PI3K/AKT/mTOR pathways

SR Hosford, TW Miller - Pharmacogenomics and personalized …, 2014 - Taylor & Francis
Breast cancers expressing estrogen receptor α, progesterone receptor, or the human
epidermal growth factor receptor 2 (HER2) proto-oncogene account for approximately 90 …