Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/107660
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dc.contributor.authorLima, Ana Rita-
dc.contributor.authorSantos, Liliana-
dc.contributor.authorCorreia, Marcelo-
dc.contributor.authorSoares, Paula-
dc.contributor.authorSobrinho-Simões, Manuel-
dc.contributor.authorMelo, Miguel-
dc.contributor.authorMáximo, Valdemar-
dc.date.accessioned2023-07-26T09:57:35Z-
dc.date.available2023-07-26T09:57:35Z-
dc.date.issued2018-02-21-
dc.identifier.issn2073-4425pt
dc.identifier.urihttps://hdl.handle.net/10316/107660-
dc.description.abstractMitochondrial dynamics are known to have an important role in so-called age-related diseases, including cancer. Mitochondria is an organelle involved in many key cellular functions and responds to physiologic or stress stimuli by adapting its structure and function. Perhaps the most important structural changes involve mitochondrial dynamics (fission and fusion), which occur in normal cells as well as in cells under dysregulation, such as cancer cells. Dynamin-related protein 1 (DRP1), a member of the dynamin family of guanosine triphosphatases (GTPases), is the key component of mitochondrial fission machinery. Dynamin-related protein 1 is associated with different cell processes such as apoptosis, mitochondrial biogenesis, mitophagy, metabolism, and cell proliferation, differentiation, and transformation. The role of DRP1 in tumorigenesis may seem to be paradoxical, since mitochondrial fission is a key mediator of two very different processes, cellular apoptosis and cell mitosis. Dynamin-related protein 1 has been associated with the development of distinct human cancers, including changes in mitochondrial energetics and cellular metabolism, cell proliferation, and stem cell maintenance, invasion, and promotion of metastases. However, the underlying mechanism for this association is still being explored. Herein, we review the published knowledge on the role of DRP1 in cancer, exploring its interaction with different biological processes in the tumorigenesis context.pt
dc.language.isoengpt
dc.publisherMDPIpt
dc.relationThis work was supported by Portuguese funds through FCT—Fundação para a Ciência e a Tecnologia—in the framework of project UID/BIM/04293/2013. It was also financed by FEDER—Fundo Europeu de Desenvolvimento Regional funds through the COMPETE 2020—Operational Program for Competitiveness and Internationalization (POCI), Portugal 2020, and by Portuguese funds through FCT—Fundação para a Ciência e Tecnologia/Ministério da Ciência, Tecnologia e Inovação in the framework of the projects “Institute for Research and Innovation in Health Sciences” (POCI-01-0145-FEDER- 007274). Further funding was obtained from the project “Advancing cancer research: from basic knowledgment to application” NORTE-01- 0145-FEDER-000029: “Projetos Estruturados de I & D & I”, funded by Norte 2020—Programa Operacional Regional do Norte.pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectdynamin-related protein 1pt
dc.subjectmitochondrial biogenesispt
dc.subjecttumorigenesispt
dc.subjectcancerpt
dc.subjectmetabolismpt
dc.titleDynamin-Related Protein 1 at the Crossroads of Cancerpt
dc.typearticle-
degois.publication.firstPage115pt
degois.publication.issue2pt
degois.publication.titleGenespt
dc.peerreviewedyespt
dc.identifier.doi10.3390/genes9020115pt
degois.publication.volume9pt
dc.date.embargo2018-02-21*
uc.date.periodoEmbargo0pt
item.grantfulltextopen-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypearticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextCom Texto completo-
Appears in Collections:FMUC Medicina - Artigos em Revistas Internacionais
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