Deubiquitinating enzymes as cancer biomarkers: new therapeutic opportunities?


Journal

BMB reports
ISSN: 1976-670X
Titre abrégé: BMB Rep
Pays: Korea (South)
ID NLM: 101465334

Informations de publication

Date de publication:
Mar 2019
Historique:
received: 10 01 2019
pubmed: 15 2 2019
medline: 2 7 2019
entrez: 15 2 2019
Statut: ppublish

Résumé

Cancer remains a life-threatening disease and accounts for the major mortality rates worldwide. The practice of using biomarkers for early detection, staging, and customized therapy may increase cancer patients' survival. Deubiquitinating enzymes (DUBs) are a family of proteases that remove ubiquitin tags from proteins of interest undergoing proteasomal degradation. DUBs play several functional roles other than deubiquitination. One of the important roles of DUBs is regulation of tumor progression. Several reports have suggested that the DUB family members were highly-elevated in various cancer cells and tissues in different stages of cancer. These findings suggest that the DUBs could be used as drug targets in cancer therapeutics. In this review, we recapitulate the role of the DUB family members, including ubiquitinspecific protease, otubain protease, and important candidates from other family members. Our aim was to better understand the connection between DUB expression profiles and cancers to allow researchers to design inhibitors or gene therapies to improve diagnosis and prognosis of cancers. [BMB Reports 2019; 52(3): 181-189].

Identifiants

pubmed: 30760385
pii: 4539
pmc: PMC6476481

Substances chimiques

Biomarkers, Tumor 0
Ubiquitin 0
Endopeptidases EC 3.4.-
Peptide Hydrolases EC 3.4.-
Deubiquitinating Enzymes EC 3.4.19.12

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

181-189

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Auteurs

Naresh Poondla (N)

Graduate School of Biomedical Science and Engineering, Department of Biomedical Science, Hanyang University, Seoul 04763, Korea.

Arun Pandian Chandrasekaran (AP)

Graduate School of Biomedical Science and Engineering, Department of Biomedical Science, Hanyang University, Seoul 04763, Korea.

Kye-Seong Kim (KS)

Graduate School of Biomedical Science and Engineering, Department of Biomedical Science, Hanyang University, Seoul 04763; College of Medicine, Hanyang University, Seoul 04763, Korea.

Suresh Ramakrishna (S)

Graduate School of Biomedical Science and Engineering, Department of Biomedical Science, Hanyang University, Seoul 04763; College of Medicine, Hanyang University, Seoul 04763, Korea.

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Classifications MeSH