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Putting the brakes on the cell cycle: mechanisms of cellular growth arrest.
Pack, Lindsey R; Daigh, Leighton H; Meyer, Tobias.
Afiliação
  • Pack LR; Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Daigh LH; Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Meyer T; Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA 94305, USA. Electronic address: tobias1@stanford.edu.
Curr Opin Cell Biol ; 60: 106-113, 2019 10.
Article em En | MEDLINE | ID: mdl-31252282
ABSTRACT
Precise regulation of cellular proliferation is critical to tissue homeostasis and development, but misregulation leads to diseases of excess proliferation or cell loss. To achieve precise control, cells utilize distinct mechanisms of growth arrest such as quiescence and senescence. The decision to enter these growth-arrested states or proliferate is mediated by the core cell-cycle machinery that responds to diverse external and internal signals. Recent advances have revealed the molecular underpinnings of these cell-cycle decisions, highlighting the unique nature of cell-cycle entry from quiescence, identifying endogenous DNA damage as a quiescence-inducing signal, and establishing how persistent arrest is achieved in senescence.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ciclo Celular / Pontos de Checagem do Ciclo Celular Idioma: En Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ciclo Celular / Pontos de Checagem do Ciclo Celular Idioma: En Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos