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Evaluation of RRAS2 and TTP1 promoter mutations in thyroid tumours

dc.contributor.authorLeite, Rúben
dc.contributor.authorDias, Carolina
dc.contributor.authorSoares, Paula
dc.contributor.authorVinagre, João
dc.date.accessioned2024-12-16T15:28:13Z
dc.date.available2024-12-16T15:28:13Z
dc.date.issued2023-05
dc.description.abstractThyroid cancer is the most frequent endocrine neoplasm, being the tenth most prevalent in both genders and it presenting an overall good prognosis [1]. Ras related 2 (R-Ras2), also known as TC21, is a GTP-binding protein that together with R-Ras1 and R-Ras3, is part of the R-Ras GTPase subfamily. Mutations in RRAS2 gene in the long-tailed hotspot Q72L/H block the hydrolysis of guanosine triphosphate (GTP) in Ras superfamily proteins, generating constitutively active proteins that will preferentially bound to GTP [2]. This gene is composed by five exons encoding a member of the Ras superfamily that participates in the RAS-MAPK pathway [3]. The tripeptidyl peptidase 1 promoter (TPP1p) encodes the telomere-binding protein TPP1 that recruits telomerase to the telomeres. This process plays a key role in the telomere stability and length regulation. Mutations in this promoter were reported to create novel transcription factor binding sites as previously presented for telomerase promoter (TERTp) [4]. Co-expression of these two promoters lead to telomere elongation, indicating that mutations in the TPP1 and TERT promoter cooperate for the immortalisation of cancer cells [5]. Our project aimed to evaluate mutations in the Q72L hotspot of the RRAS2 gene and in the TPP1p in thyroid tumours. Upon genotyping of RRas2 and TPP1p, we conclude that the presence of mutations in the Q72L hotspot may not represent an oncogenic event, as we did not detect them. For TPP1p, still under study, although already presented in the literature, at the moment we have not detected them in our series, pointing that they may be a rare event in thyroid tumours.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationLeite, R., Dias, C., Soares, P., & Vinagre, J. (2023). Evaluation of RRAS2 and TTP1 promoter mutations in thyroid tumours. Livro de Resumos do 16º Encontro de Investigação Jovem da U.Porto / Book of Abstracts Young Researchers Meeting of U.Porto, 838–839.pt_PT
dc.identifier.isbn978-989-746-356-3
dc.identifier.urihttp://hdl.handle.net/10400.22/26867
dc.language.isoengpt_PT
dc.publisherUniversidade do Portopt_PT
dc.relationThis study is part of the project "Cancer Research on Therapy Resistance: From Basic Mechanisms to Novel Targets"—NORTE-01-0145-FEDER-000051, and was supported on the context of "The Porto Comprehensive Cancer Center" with the reference NORTE-01-0145-FEDER-072678 - Consórcio PORTO.CCC – Porto.Comprehensive Cancer Center Raquel Seruca, by Norte Portugal Regional Operational Programme (NORTE 2020), under the PORTUGAL 2020 Partnership Agreement, through the European Regional Development Fund (ERDF).pt_PT
dc.relation.publisherversionhttps://www.up.pt/ijup/wp-content/uploads/sites/892/2023/06/Livro-de-Resumos_final.pdfpt_PT
dc.subjectThyroid cancerpt_PT
dc.subjectTumourspt_PT
dc.subjectR-Ras2 genept_PT
dc.subjectQ72L hotspotpt_PT
dc.subjectTelomerase promoter (TERTp)pt_PT
dc.subjectTPP1 promotor (TPP1p)pt_PT
dc.titleEvaluation of RRAS2 and TTP1 promoter mutations in thyroid tumourspt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlacePortopt_PT
oaire.citation.endPage839pt_PT
oaire.citation.startPage838pt_PT
oaire.citation.titleLivro de Resumos do 16.º Encontro de Investigação Jovem da U.Porto / Book of Abstracts Young Researchers Meeting of U.Portopt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typeconferenceObjectpt_PT

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