Literature DB >> 25088039

Deubiquitinating enzyme inhibitors and their potential in cancer therapy.

Bernat Crosas1.   

Abstract

Deubiquitinating enzymes (or DUBs) attack the ubiquitin-based isopeptide bond, thus counteracting ubiquitinprotein ligase activity in vivo. By disassembling ubiquitin-substrate and ubiquitin-ubiquitin covalent links, deubiquitinating enzymes exert a very powerful control of many signaling processes within the ubiquitin-proteasome system (UPS). Very active research in this field in the last decade shows that deubiquitinating enzymes play important regulatory roles in aspects relevant to cancer, such as proteasome activity, p53 stability, the regulation of fanconi anemia related proteins, tumor cell apoptosis induction, to mention a few. Thus, deubiquitinating enzymes have emerged as interesting drug targets in cancer research. Here, the pharmacological inhibition of DUBs and its potential effect in cancer treatment are reviewed.

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Year:  2014        PMID: 25088039     DOI: 10.2174/1568009614666140725090620

Source DB:  PubMed          Journal:  Curr Cancer Drug Targets        ISSN: 1568-0096            Impact factor:   3.428


  11 in total

Review 1.  Deubiquitinases (DUBs) and DUB inhibitors: a patent review.

Authors:  Pershang Farshi; Rahul R Deshmukh; Joseph O Nwankwo; Richard T Arkwright; Boris Cvek; Jinbao Liu; Q Ping Dou
Journal:  Expert Opin Ther Pat       Date:  2015-06-16       Impact factor: 6.674

2.  IGF-1 promotes the growth and metastasis of hepatocellular carcinoma via the inhibition of proteasome-mediated cathepsin B degradation.

Authors:  Tian Lei; Xie Ling
Journal:  World J Gastroenterol       Date:  2015-09-21       Impact factor: 5.742

Review 3.  The role of deubiquitinating enzymes in cancer drug resistance.

Authors:  Parthasaradhireddy Tanguturi; Kye-Seong Kim; Suresh Ramakrishna
Journal:  Cancer Chemother Pharmacol       Date:  2020-03-07       Impact factor: 3.333

4.  Simultaneous inhibition of deubiquitinating enzymes (DUBs) and autophagy synergistically kills breast cancer cells.

Authors:  Rachel Isaksson Vogel; Kathleen Coughlin; Alessandra Scotti; Yoshie Iizuka; Ravi Anchoori; Richard B S Roden; Mauro Marastoni; Martina Bazzaro
Journal:  Oncotarget       Date:  2015-02-28

Review 5.  Neuroinflammation and J2 prostaglandins: linking impairment of the ubiquitin-proteasome pathway and mitochondria to neurodegeneration.

Authors:  Maria E Figueiredo-Pereira; Patricia Rockwell; Thomas Schmidt-Glenewinkel; Peter Serrano
Journal:  Front Mol Neurosci       Date:  2015-01-13       Impact factor: 5.639

6.  Ataxin-3 like (ATXN3L), a member of the Josephin family of deubiquitinating enzymes, promotes breast cancer proliferation by deubiquitinating Krüppel-like factor 5 (KLF5).

Authors:  Fei Ge; Wenlin Chen; Junying Qin; Zhongmei Zhou; Rong Liu; Linlin Liu; Jing Tan; Tianning Zou; Hongyuan Li; Guosheng Ren; Ceshi Chen
Journal:  Oncotarget       Date:  2015-08-28

7.  Neurotoxic mechanisms by which the USP14 inhibitor IU1 depletes ubiquitinated proteins and Tau in rat cerebral cortical neurons: Relevance to Alzheimer's disease.

Authors:  Magdalena J Kiprowska; Anna Stepanova; Dustin R Todaro; Alexander Galkin; Arthur Haas; Scott M Wilson; Maria E Figueiredo-Pereira
Journal:  Biochim Biophys Acta Mol Basis Dis       Date:  2017-04-01       Impact factor: 5.187

8.  Expression Atlas of the Deubiquitinating Enzymes in the Adult Mouse Retina, Their Evolutionary Diversification and Phenotypic Roles.

Authors:  Mariona Esquerdo; Xavier Grau-Bové; Alejandro Garanto; Vasileios Toulis; Sílvia Garcia-Monclús; Erica Millo; Ma José López-Iniesta; Víctor Abad-Morales; Iñaki Ruiz-Trillo; Gemma Marfany
Journal:  PLoS One       Date:  2016-03-02       Impact factor: 3.240

9.  An OTU deubiquitinating enzyme in Eimeria tenella interacts with Eimeria tenella virus RDRP.

Authors:  Pu Wang; Jianhua Li; Pengtao Gong; Weirong Wang; Yongxing Ai; Xichen Zhang
Journal:  Parasit Vectors       Date:  2018-01-31       Impact factor: 3.876

Review 10.  USP14: Structure, Function, and Target Inhibition.

Authors:  Feng Wang; Shuo Ning; Beiming Yu; Yanfeng Wang
Journal:  Front Pharmacol       Date:  2022-01-05       Impact factor: 5.810

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