Exploiting S-nitrosylation for cancer therapy: facts and perspectives.


Journal

The Biochemical journal
ISSN: 1470-8728
Titre abrégé: Biochem J
Pays: England
ID NLM: 2984726R

Informations de publication

Date de publication:
16 10 2020
Historique:
received: 26 05 2020
revised: 02 09 2020
accepted: 07 09 2020
entrez: 5 10 2020
pubmed: 6 10 2020
medline: 24 2 2021
Statut: ppublish

Résumé

S-nitrosylation, the post-translational modification of cysteines by nitric oxide, has been implicated in several cellular processes and tissue homeostasis. As a result, alterations in the mechanisms controlling the levels of S-nitrosylated proteins have been found in pathological states. In the last few years, a role in cancer has been proposed, supported by the evidence that various oncoproteins undergo gain- or loss-of-function modifications upon S-nitrosylation. Here, we aim at providing insight into the current knowledge about the role of S-nitrosylation in different aspects of cancer biology and report the main anticancer strategies based on: (i) reducing S-nitrosylation-mediated oncogenic effects, (ii) boosting S-nitrosylation to stimulate cell death, (iii) exploiting S-nitrosylation through synthetic lethality.

Identifiants

pubmed: 33017470
pii: 226585
doi: 10.1042/BCJ20200064
doi:

Substances chimiques

Nitric Oxide 31C4KY9ESH

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

3649-3672

Informations de copyright

© 2020 The Author(s). Published by Portland Press Limited on behalf of the Biochemical Society.

Auteurs

Salvatore Rizza (S)

Redox Signaling and Oxidative Stress Group, Danish Cancer Society Research Center, 2100 Copenhagen, Denmark.

Giuseppe Filomeni (G)

Redox Signaling and Oxidative Stress Group, Danish Cancer Society Research Center, 2100 Copenhagen, Denmark.
Center for Healthy Aging, Copenhagen University, Copenhagen, Denmark.
Department of Biology, Tor Vergata University, 00133 Rome, Italy.

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Classifications MeSH