Unknown

Dataset Information

0

Recent Advances of Cell-Cycle Inhibitor Therapies for Pediatric Cancer.


ABSTRACT: This review describes the pivotal roles of cell-cycle and checkpoint regulators and discusses development of specific cell-cycle inhibitors for therapeutic use for pediatric cancer. The mechanism of action as well as the safety and tolerability of drugs in pediatric patients, including compounds that target CDK4/CDK6 (palbociclib, ribociclib, and abemaciclib), aurora kinases (AT9283 and MLN8237), Wee1 kinase (MK-1775), KSP (ispinesib), and tubulin (taxanes, vinca alkaloids), are presented. The design of mechanism-based combinations that exploit the cross-talk of signals activated by cell-cycle arrest, as well as pediatric-focused drug development, are critical for the advancement of drugs for rare childhood diseases. Cancer Res; 77(23); 6489-98. ©2017 AACR.

SUBMITTER: Mills CC 

PROVIDER: S-EPMC5712276 | biostudies-literature | 2017 Dec

REPOSITORIES: biostudies-literature

altmetric image

Publications

Recent Advances of Cell-Cycle Inhibitor Therapies for Pediatric Cancer.

Mills Christopher C CC   Kolb E A EA   Sampson Valerie B VB  

Cancer research 20171102 23


This review describes the pivotal roles of cell-cycle and checkpoint regulators and discusses development of specific cell-cycle inhibitors for therapeutic use for pediatric cancer. The mechanism of action as well as the safety and tolerability of drugs in pediatric patients, including compounds that target CDK4/CDK6 (palbociclib, ribociclib, and abemaciclib), aurora kinases (AT9283 and MLN8237), Wee1 kinase (MK-1775), KSP (ispinesib), and tubulin (taxanes, vinca alkaloids), are presented. The d  ...[more]

Similar Datasets

| S-EPMC5138135 | biostudies-literature
| S-EPMC8417143 | biostudies-literature
| S-EPMC7555943 | biostudies-literature
| S-EPMC4042838 | biostudies-literature
| S-EPMC4024386 | biostudies-literature
| S-EPMC5365224 | biostudies-literature
| S-EPMC8428367 | biostudies-literature
| S-EPMC7886057 | biostudies-literature
| S-EPMC7308880 | biostudies-literature
| S-EPMC4404436 | biostudies-literature