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How does caspases regulation play role in cell decisions? apoptosis and beyond.
Ghorbani, Negar; Yaghubi, Roham; Davoodi, Jamshid; Pahlavan, Sara.
Afiliação
  • Ghorbani N; Department of Biochemistry, Institute of Biochemistry and Biophysics, University of Tehran, Tehran, Iran.
  • Yaghubi R; Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran.
  • Davoodi J; Department of Biochemistry, Institute of Biochemistry and Biophysics, University of Tehran, Tehran, Iran. jamshid_davoodi@hotmail.com.
  • Pahlavan S; Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran. sarapahlavan@royaninstitute.org.
Mol Cell Biochem ; 2023 Nov 17.
Article em En | MEDLINE | ID: mdl-37976000
ABSTRACT
Caspases are a family of cysteine proteases, and the key factors behind the cellular events which occur during apoptosis and inflammation. However, increasing evidence shows the non-conventional pro-survival action of apoptotic caspases in crucial processes. These cellular events include cell proliferation, differentiation, and migration, which may appear in the form of metastasis, and chemotherapy resistance in cancerous situations. Therefore, there should be a precise and strict control of caspases activity, perhaps through maintaining the threshold below the required levels for apoptosis. Thus, understanding the regulators of caspase activities that render apoptotic caspases as non-apoptotic is of paramount importance both mechanistically and clinically. Furthermore, the functions of apoptotic caspases are affected by numerous post-translational modifications. In the present mini-review, we highlight the various mechanisms that directly impact caspases with respect to their anti- or non-apoptotic functions. In this regard, post-translational modifications (PTMs), isoforms, subcellular localization, transient activity, substrate availability, substrate selection, and interaction-mediated regulations are discussed.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article