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dc.contributor.authorSalinee Jantrapiromen_US
dc.contributor.authorLuca Lo Piccoloen_US
dc.contributor.authorDumnoensun Pruksakornen_US
dc.contributor.authorSaranyapin Potikanonden_US
dc.contributor.authorWutigri Nimlamoolen_US
dc.date.accessioned2020-10-14T08:25:46Z-
dc.date.available2020-10-14T08:25:46Z-
dc.date.issued2020-06-01en_US
dc.identifier.issn20726694en_US
dc.identifier.other2-s2.0-85088485114en_US
dc.identifier.other10.3390/cancers12061586en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85088485114&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/70219-
dc.description.abstract© 2020 by the authors. Licensee MDPI, Basel, Switzerland. Ubiquilins or UBQLNs, members of the ubiquitin-like and ubiquitin-associated domain (UBL-UBA) protein family, serve as adaptors to coordinate the degradation of specific substrates via both proteasome and autophagy pathways. The UBQLN substrates reveal great diversity and impact a wide range of cellular functions. For decades, researchers have been attempting to uncover a puzzle and understand the role of UBQLNs in human cancers, particularly in the modulation of oncogene’s stability and nucleotide excision repair. In this review, we summarize the UBQLNs’ genetic variants that are associated with the most common cancers and also discuss their reliability as a prognostic marker. Moreover, we provide an overview of the UBQLNs networks that are relevant to cancers in different ways, including cell cycle, apoptosis, epithelial-mesenchymal transition, DNA repairs and miRNAs. Finally, we include a future prospective on novel ubiquilin-based cancer therapies.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleUbiquilin networking in cancersen_US
dc.typeJournalen_US
article.title.sourcetitleCancersen_US
article.volume12en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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