[HTML][HTML] The RB and p53 pathways in cancer

CJ Sherr, F McCormick - Cancer cell, 2002 - cell.com
The life history of cancer cells encompasses a series of genetic missteps in which normal
cells are progressively transformed into tumor cells that invade surrounding tissues and …

Protein kinases as targets for anticancer agents: from inhibitors to useful drugs

D Fabbro, S Ruetz, E Buchdunger… - Pharmacology & …, 2002 - Elsevier
Many components of mitogenic signaling pathways in normal and neoplastic cells have
been identified, including the large family of protein kinases, which function as components …

Specific inhibition of cyclin-dependent kinase 4/6 by PD 0332991 and associated antitumor activity in human tumor xenografts

DW Fry, PJ Harvey, PR Keller, WL Elliott… - Molecular cancer …, 2004 - AACR
PD 0332991 is a highly specific inhibitor of cyclin-dependent kinase 4 (Cdk4)(IC50, 0.011
μmol/L) and Cdk6 (IC50, 0.016 μmol/L), having no activity against a panel of 36 additional …

Discovery of a potent and selective inhibitor of cyclin-dependent kinase 4/6

PL Toogood, PJ Harvey, JT Repine… - Journal of medicinal …, 2005 - ACS Publications
A pharmacological approach to inhibition of cyclin-dependent kinases 4 and 6 (Cdk4/6)
using highly selective small molecule inhibitors has the potential to provide novel cancer …

Proliferation of cancer cells despite CDK2 inhibition

O Tetsu, F McCormick - Cancer cell, 2003 - cell.com
We have investigated the contribution of CDK4 and CDK2 inhibition to G1 arrest in colon
cancers following inhibition of the MEK/MAP kinase pathway. CDK4 inhibition is sufficient to …

3‐alkenyl‐oxindoles: natural products, pharmaceuticals, and recent synthetic advances in tandem/telescoped approaches

A Millemaggi, RJK Taylor - European Journal of Organic …, 2010 - Wiley Online Library
The structures and biological activities of naturally occurring 3‐alkenyl‐oxindoles are
reviewed. Important man‐made3‐alkenyl‐oxindoles are covered, particularly those with …

Molecular mechanisms of indirubin and its derivatives: novel anticancer molecules with their origin in traditional Chinese phytomedicine

G Eisenbrand, F Hippe, S Jakobs… - Journal of cancer research …, 2004 - Springer
Abstract Indirubin, a 3, 2'bisindole isomer of indigo, has originally been identified as the
active principle of a traditional Chinese preparation and has been proven to exhibit …

Cyclin E1 and Rb modulation as common events at time of resistance to palbociclib in hormone receptor-positive breast cancer

C Guarducci, M Bonechi, M Benelli, C Biagioni… - NPJ breast …, 2018 - nature.com
CDK4/6 inhibitors represent a new treatment standard for hormone receptor-positive (HR+),
HER2-negative advanced breast cancer (BC) patients. Although efficacious, resistance to …

Pyrido[2,3-d]pyrimidin-7-ones as Specific Inhibitors of Cyclin-Dependent Kinase 4

SN VanderWel, PJ Harvey, DJ McNamara… - Journal of medicinal …, 2005 - ACS Publications
Inhibition of the cell cycle kinase, cyclin-dependent kinase-4 (Cdk4), is expected to provide
an effective method for the treatment of proliferative diseases such as cancer. The pyrido [2 …

CDK4/6 inhibitors in combination therapies: better in company than alone: a mini review

GL Rampioni Vinciguerra, M Sonego, I Segatto… - Frontiers in …, 2022 - frontiersin.org
The cyclin D-CDK4/6 complexes play a pivotal role in controlling the cell cycle. Deregulation
in cyclin D-CDK4/6 pathway has been described in many types of cancer and it invariably …