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Beyond Kinases: Targeting Replication Stress Proteins in Cancer Therapy.
Baillie, Katherine E; Stirling, Peter C.
Afiliação
  • Baillie KE; Terry Fox Laboratory, BC Cancer, Vancouver, BC, Canada.
  • Stirling PC; Terry Fox Laboratory, BC Cancer, Vancouver, BC, Canada; Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada. Electronic address: pstirling@bccrc.ca.
Trends Cancer ; 7(5): 430-446, 2021 05.
Article em En | MEDLINE | ID: mdl-33203609
DNA replication stress describes a state of impaired replication fork progress that triggers a cellular stress response to maintain genome stability and complete DNA synthesis. Replication stress is a common state that must be tolerated in many cancers. One promising therapeutic approach is targeting replication stress response factors such as the ataxia telangiectasia and rad 3-related kinase (ATR) or checkpoint kinase 1 (CHK1) kinases that some cancers depend upon to survive endogenous replication stress. However, research revealing the complexity of the replication stress response suggests new genetic interactions and candidate therapeutic targets. Many of these candidates regulate DNA transactions around reversed replication forks, including helicases, nucleases and alternative polymerases that promote fork stability and restart. Here we review emerging strategies to exploit replication stress for cancer therapy.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Proteínas de Ligação a DNA / Reparo do DNA / Replicação do DNA / Neoplasias Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Proteínas de Ligação a DNA / Reparo do DNA / Replicação do DNA / Neoplasias Idioma: En Ano de publicação: 2021 Tipo de documento: Article