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Signal Transduction Pathways Regulating the Alternative Splicing of Tumor Related RAC1b

dc.contributor.authorGonçalves, Vânia
dc.contributor.authorMatos, Paulo
dc.contributor.authorJordan, Peter
dc.date.accessioned2020-06-07T17:00:17Z
dc.date.available2020-06-07T17:00:17Z
dc.date.issued2019-10-19
dc.description.abstractDistinct genetic subtypes have been described in colon cancer, one of which involves overexpression of RAC1b, a variant generated by alternative splicing. Aberrant splicing is known to occur in cancer and can be caused by mutation in a gene or splicing factor but also represents a dynamic response to oncogene-induced cellular signaling and in this case it may be pharmacologically targeted. Here we explore how signaling pathways are involved in the deregulation of alternative RAC1b splicing in colorectal tumor cells. HT29 cells represent serrated colorectal tumors with BRAF gene mutation V600E in one allele and RAC1b overexpression. Cells were transfected with shRNA vectors directed against target candidate protein kinase transcripts and their effects on RAC1b levels analyzed 24h later by Western Blot and qRT-PCR. Treatment with kinase inhibitors or anti-inflammatory drugs was performed 24h and 48h prior to cell lysis. Two kinases, SRPK1 and GSK3β, were found required to sustain RAC1b levels and both were shown to act upon the phosphorylation of splicing factor SRSF1, which binds to and promotes the inclusion of the alternative exon in RAC1b. SRPK1 knockdown or pharmacological inhibition reduced SRSF1 phosphorylation decreasing its nuclear translocation and concomitantly RAC1b splicing. The same regulatory pathway was also found to be controlled by GSK3β. Interestingly, GSK3β phosphorylation was identified to serve as target for the anti-inflammatory drug ibuprofen, which inhibits RAC1b overexpression. Together, our results demonstrate that alternative splicing is deregulated by oncogenic signal transduction pathways and it may be drug revertable.pt_PT
dc.description.sponsorshipFCT PTDC/BIA-MOL/28386/2017pt_PT
dc.description.versionN/Apt_PT
dc.identifier.urihttp://hdl.handle.net/10400.18/6945
dc.language.isoengpt_PT
dc.subjectAlternative Splicingpt_PT
dc.subjectRAC1bpt_PT
dc.subjectColrectal Cancerpt_PT
dc.subjectVias de Transdução de Sinal e Patologias Associadaspt_PT
dc.titleSignal Transduction Pathways Regulating the Alternative Splicing of Tumor Related RAC1bpt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceFaro, Portugalpt_PT
oaire.citation.title10th Meeting on Signal Transduction SINAL 2019, 18-19 outubro 2019pt_PT
rcaap.rightsembargoedAccesspt_PT
rcaap.typeconferenceObjectpt_PT

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