j 2023

Therapeutic potential of CDK11 in cancer

BLAŽEK, Dalibor

Basic information

Original name

Therapeutic potential of CDK11 in cancer

Edition

CLINICAL AND TRANSLATIONAL MEDICINE, ENGLAND, JOHN WILEY & SONS LTD, 2023, 2001-1326

Other information

Language

English

Type of outcome

Article in a journal (not reviewed)

Field of Study

30204 Oncology

Confidentiality degree

is not subject to a state or trade secret

References:

Impact factor

Impact factor: 7.900

RIV identification code

RIV/00216224:14740/23:00139568

Organization unit

Central European Institute of Technology

UT WoS

000940411100001

Keywords in English

cancer; CDK11; OTS964; pladienolide B; spliceosome; splicing

Tags

Tags

International impact
Changed: 4/4/2025 16:14, Mgr. Eva Dubská

Abstract

In the original language

Human cyclin-dependent kinases (CDKs) direct the progression of the cell cycle and transcription. They are deregulated in tumours, and despite their involvement in the regulation of basic cellular processes, many CDKs are promising targets for cancer therapy. CDK11 is an essential gene for the growth of many malignancies; however, its primary cellular function has been obscure, and the mode-of-action of OTS964, the first CDK11 inhibitor and antiproliferative compound, has been unknown. A recent study has shown that OTS964 prevents spliceosome activation, revealing a key role of CDK11 in the regulation of pre-mRNA splicing. In light of these findings, we discuss the therapeutic potential of CDK11 in cancer.

Links

GA21-19266S, research and development project
Name: Charakterizace kinazové aktivity cyklin dependentní kinázy 11 (CDK11), enzymu nezbytného pro růst nádorů
Investor: Czech Science Foundation, Characterization of kinase activity of cyclin-dependent kinase 11 (CDK11), an essential enzyme for the growth of cancer
GX23-04754X, research and development project
Name: Identifikace a charakterizace nové signální dráhy regulující sestřih pre-mRNA
Investor: Czech Science Foundation, Identification and characterization of a new pathway regulating pre-mRNA splicing