Literature DB >> 31395352

Poly-ADP ribosylation in DNA damage response and cancer therapy.

Wei-Hsien Hou1, Shih-Hsun Chen2, Xiaochun Yu3.   

Abstract

Poly(ADP-ribosyl)ation (aka PARylation) is a unique protein post-translational modification (PTM) first described over 50 years ago. PARylation regulates a number of biological processes including chromatin remodeling, the DNA damage response (DDR), transcription, apoptosis, and mitosis. The subsequent discovery of poly(ADP-ribose) polymerase-1 (PARP-1) catalyzing DNA-dependent PARylation spearheaded the field of DDR. The expanding knowledge about the poly ADP-ribose (PAR) recognition domains prompted the discovery of novel DDR factors and revealed crosstalk with other protein PTMs including phosphorylation, ubiquitination, methylation and acetylation. In this review, we highlight the current knowledge on PAR-regulated DDR, PAR recognition domain, and PARP inhibition in cancer therapy.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  BRCT domain; DNA damage response; De-PARylation; PAR recognition domain; PARP inhibitor; PARP inhibitor resistance; PARylation; Poly(ADP-ribosyl)ation; Poly(ADP-ribosyl)lation polymerase

Mesh:

Substances:

Year:  2017        PMID: 31395352      PMCID: PMC6690395          DOI: 10.1016/j.mrrev.2017.09.004

Source DB:  PubMed          Journal:  Mutat Res Rev Mutat Res        ISSN: 1383-5742            Impact factor:   5.657


  147 in total

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Authors:  D D'Amours; S Desnoyers; I D'Silva; G G Poirier
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Review 2.  The diverse roles and clinical relevance of PARPs in DNA damage repair: current state of the art.

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Journal:  Biochem Pharmacol       Date:  2012-03-31       Impact factor: 5.858

3.  Genetic interaction between PARP and DNA-PK in V(D)J recombination and tumorigenesis.

Authors:  C Morrison; G C Smith; L Stingl; S P Jackson; E F Wagner; Z Q Wang
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5.  The BRCT domain is a phospho-protein binding domain.

Authors:  Xiaochun Yu; Claudia Christiano Silva Chini; Miao He; Georges Mer; Junjie Chen
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6.  Preclinical selection of a novel poly(ADP-ribose) polymerase inhibitor for clinical trial.

Authors:  Huw D Thomas; Christopher R Calabrese; Michael A Batey; Stacie Canan; Zdenek Hostomsky; Suzanne Kyle; Karen A Maegley; David R Newell; Donald Skalitzky; Lan-Zhen Wang; Stephen E Webber; Nicola J Curtin
Journal:  Mol Cancer Ther       Date:  2007-03       Impact factor: 6.261

7.  Processing of protein ADP-ribosylation by Nudix hydrolases.

Authors:  Luca Palazzo; Benjamin Thomas; Ann-Sofie Jemth; Thomas Colby; Orsolya Leidecker; Karla L H Feijs; Roko Zaja; Olga Loseva; Jordi Carreras Puigvert; Ivan Matic; Thomas Helleday; Ivan Ahel
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9.  CHFR is important for the first wave of ubiquitination at DNA damage sites.

Authors:  Chao Liu; Jiaxue Wu; Sharad C Paudyal; Zhongsheng You; Xiaochun Yu
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10.  A family of macrodomain proteins reverses cellular mono-ADP-ribosylation.

Authors:  Gytis Jankevicius; Markus Hassler; Barbara Golia; Vladimir Rybin; Martin Zacharias; Gyula Timinszky; Andreas G Ladurner
Journal:  Nat Struct Mol Biol       Date:  2013-03-10       Impact factor: 15.369

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2.  Pre-ribosomal RNA reorganizes DNA damage repair factors in nucleus during meiotic prophase and DNA damage response.

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Review 3.  Protein post-translational modifications in the regulation of cancer hallmarks.

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Journal:  Cancer Gene Ther       Date:  2022-04-07       Impact factor: 5.854

Review 4.  Brain on food: The neuroepigenetics of nutrition.

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Review 5.  Mitochondrial Protection by PARP Inhibition.

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Journal:  Int J Mol Sci       Date:  2020-04-16       Impact factor: 5.923

Review 6.  The Enigmatic Function of PARP1: From PARylation Activity to PAR Readers.

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8.  Clinical PARP inhibitors do not abrogate PARP1 exchange at DNA damage sites in vivo.

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9.  mTOR may interact with PARP-1 to regulate visible light-induced parthanatos in photoreceptors.

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Review 10.  A New Twist in Protein Kinase B/Akt Signaling: Role of Altered Cancer Cell Metabolism in Akt-Mediated Therapy Resistance.

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