Publication
Alternative Splicing: Expanding the Landscape of Cancer Biomarkers and Therapeutics
| dc.contributor.author | Bessa, Cláudia | |
| dc.contributor.author | Matos, Paulo | |
| dc.contributor.author | Jordan, Peter | |
| dc.contributor.author | Gonçalves, Vânia | |
| dc.date.accessioned | 2021-03-06T15:23:01Z | |
| dc.date.available | 2021-03-06T15:23:01Z | |
| dc.date.issued | 2020-11-27 | |
| dc.description | This article belongs to the Special Issue Targeting Dysregulated RNA Processing in Cancer | pt_PT |
| dc.description.abstract | Alternative splicing (AS) is a critical post-transcriptional regulatory mechanism used by more than 95% of transcribed human genes and responsible for structural transcript variation and proteome diversity. In the past decade, genome-wide transcriptome sequencing has revealed that AS is tightly regulated in a tissue- and developmental stage-specific manner, and also frequently dysregulated in multiple human cancer types. It is currently recognized that splicing defects, including genetic alterations in the spliced gene, altered expression of both core components or regulators of the precursor messenger RNA (pre-mRNA) splicing machinery, or both, are major drivers of tumorigenesis. Hence, in this review we provide an overview of our current understanding of splicing alterations in cancer, and emphasize the need to further explore the cancer-specific splicing programs in order to obtain new insights in oncology. Furthermore, we also discuss the recent advances in the identification of dysregulated splicing signatures on a genome-wide scale and their potential use as biomarkers. Finally, we highlight the therapeutic opportunities arising from dysregulated splicing and summarize the current approaches to therapeutically target AS in cancer. | pt_PT |
| dc.description.sponsorship | Work in the authors’ laboratory was supported by Fundação para a Ciência e a Tecnologia (FCT), Portugal (through grant UID/MULTI/04046/2019 to Research Unit BioISI since January 2019 and grant PTDC/BIA-MOL/28386/2017 to V.G. since October 2018) and by the Portuguese association Maratona da Saúde—Cancro 2014 to P.J. since January 2016. | pt_PT |
| dc.description.version | info:eu-repo/semantics/publishedVersion | pt_PT |
| dc.identifier.citation | Int J Mol Sci. 2020 Nov 27;21(23):9032. doi: 10.3390/ijms21239032. | pt_PT |
| dc.identifier.doi | 10.3390/ijms21239032 | pt_PT |
| dc.identifier.issn | 1661-6596 | |
| dc.identifier.uri | http://hdl.handle.net/10400.18/7342 | |
| dc.language.iso | eng | pt_PT |
| dc.peerreviewed | yes | pt_PT |
| dc.publisher | MDPI | pt_PT |
| dc.relation.publisherversion | https://www.mdpi.com/1422-0067/21/23/9032 | pt_PT |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | pt_PT |
| dc.subject | Alternative Splicing | pt_PT |
| dc.subject | Cancer | pt_PT |
| dc.subject | Cancer Progression | pt_PT |
| dc.subject | Biomarkers | pt_PT |
| dc.subject | Mutation | pt_PT |
| dc.subject | Pre-messenger RNA | pt_PT |
| dc.subject | Signal Transduction | pt_PT |
| dc.subject | Splicing Factor | pt_PT |
| dc.subject | Therapeutic Target | pt_PT |
| dc.subject | Tumor Biology | pt_PT |
| dc.subject | Vias de Transdução de Sinal e Patologias Associadas | pt_PT |
| dc.title | Alternative Splicing: Expanding the Landscape of Cancer Biomarkers and Therapeutics | pt_PT |
| dc.type | journal article | |
| dspace.entity.type | Publication | |
| oaire.awardURI | info:eu-repo/grantAgreement/FCT/5876/UID%2FMulti%2F04046%2F2013/PT (2019) | |
| oaire.citation.issue | 23 | pt_PT |
| oaire.citation.startPage | 9032 | pt_PT |
| oaire.citation.title | International Journal of Molecular Sciences | pt_PT |
| oaire.citation.volume | 21 | pt_PT |
| oaire.fundingStream | 5876 | |
| project.funder.identifier | http://doi.org/10.13039/501100001871 | |
| project.funder.name | Fundação para a Ciência e a Tecnologia | |
| rcaap.embargofct | Acesso de acordo com política editorial da revista. | pt_PT |
| rcaap.rights | openAccess | pt_PT |
| rcaap.type | article | pt_PT |
| relation.isProjectOfPublication | 0dbd968f-ea65-4a2a-9b40-008aff7adbeb | |
| relation.isProjectOfPublication.latestForDiscovery | 0dbd968f-ea65-4a2a-9b40-008aff7adbeb |
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