Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/109712
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dc.contributorDepartment of Rehabilitation Sciences-
dc.contributorSchool of Nursing-
dc.contributorCollege of Professional and Continuing Education-
dc.creatorLui, K-
dc.creatorHuang, Y-
dc.creatorSheikh, MS-
dc.creatorCheung, KK-
dc.creatorTam, WY-
dc.creatorSun, KT-
dc.creatorCheng, KM-
dc.creatorNg, WWM-
dc.creatorLoh, AWK-
dc.date.accessioned2024-11-08T06:11:30Z-
dc.date.available2024-11-08T06:11:30Z-
dc.identifier.urihttp://hdl.handle.net/10397/109712-
dc.language.isoenen_US
dc.publisherIvyspring International Publisheren_US
dc.rights© The author(s). This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/).en_US
dc.rightsSee http://ivyspring.com/terms for full terms and conditions.en_US
dc.rightsThe following publication Lui K, Huang Y, Sheikh MS, Cheung KK, Tam WY, Sun KT, Cheng KM, Ng WWM, Loh AWK. The oncogenic potential of Rab-like protein 1A (RBEL1A) GTPase: The first review of RBEL1A research with future research directions and challenges. J Cancer 2023; 14(17):3214-3226 is available at https://doi.org/10.7150/jca.84267.en_US
dc.subjectCanceren_US
dc.subjectGTPaseen_US
dc.subjectOncogeneen_US
dc.subjectRBEL1Aen_US
dc.titleThe oncogenic potential of Rab-like protein 1A (RBEL1A) GTPase : the first review of RBEL1A research with future research directions and challengesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage3214-
dc.identifier.epage3226-
dc.identifier.volume14-
dc.identifier.issue17-
dc.identifier.doi10.7150/jca.84267-
dcterms.abstractResearch on Rab-like protein 1A (RBEL1A) in the past two decades highlighted the oncogenic properties of this gene. Despite the emerging evidence, its importance in cancer biology was underrated. This is the first RBEL1A critical review covering its discovery, biochemistry, physiological functions, and clinical insights. RBEL1A expression at the appropriate levels appears essential in normal cells and tissues to maintain chromosomal stability; however, its overexpression is linked to tumorigenesis. Furthermore, the upstream and downstream targets of the RBEL1A signaling pathways will be discussed. Mechanistically, RBEL1A promotes cell proliferation signals by enhancing the Erk1/2, Akt, c-Myc, and CDK pathways while blunting the apoptotic signals via inhibitions on p53, Rb, and caspase pathways. More importantly, this review covers the clinical relevance of RBEL1A in the cancer field, such as drug resistance and poor overall survival rate. Also, this review points out the bottle-necks of the RBEL1A research and its future research directions. It is becoming clear that RBEL1A could potentially serve as a valuable target of anticancer therapy. Genetic and pharmacological researches are expected to facilitate the identification and development of RBEL1A inhibitors as cancer therapeutics in the future, which could undoubtedly improve the management of human malignancy.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationJournal of cancer, 2023, v. 14, no. 17, p. 3214-3226-
dcterms.isPartOfJournal of cancer-
dcterms.issued2023-
dc.identifier.scopus2-s2.0-85178031915-
dc.identifier.eissn1837-9664-
dc.description.validate202411 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOSen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextFood and Health Bureau, Hong Kong Special Administrative Region (HKSAR); Hong Kong Metropolitan University; College of Professional and Continuing Education, The Hong Kong Polytechnic Universityen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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