Dynamin-Related Protein 1 at the Crossroads of Cancer

Bibliographic Details
Main Author: Lima, Ana Rita
Publication Date: 2018
Other Authors: Santos, Liliana, Correia, Marcelo, Soares, Paula, Sobrinho-Simões, Manuel, Melo, Miguel, Máximo, Valdemar
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: https://hdl.handle.net/10316/107660
https://doi.org/10.3390/genes9020115
Summary: Mitochondrial 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.
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spelling Dynamin-Related Protein 1 at the Crossroads of Cancerdynamin-related protein 1mitochondrial biogenesistumorigenesiscancermetabolismMitochondrial 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.This 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.MDPI2018-02-21info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://hdl.handle.net/10316/107660https://hdl.handle.net/10316/107660https://doi.org/10.3390/genes9020115eng2073-4425Lima, Ana RitaSantos, LilianaCorreia, MarceloSoares, PaulaSobrinho-Simões, ManuelMelo, MiguelMáximo, Valdemarinfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-09-30T15:21:26Zoai:estudogeral.uc.pt:10316/107660Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T05:58:42.774147Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Dynamin-Related Protein 1 at the Crossroads of Cancer
title Dynamin-Related Protein 1 at the Crossroads of Cancer
spellingShingle Dynamin-Related Protein 1 at the Crossroads of Cancer
Lima, Ana Rita
dynamin-related protein 1
mitochondrial biogenesis
tumorigenesis
cancer
metabolism
title_short Dynamin-Related Protein 1 at the Crossroads of Cancer
title_full Dynamin-Related Protein 1 at the Crossroads of Cancer
title_fullStr Dynamin-Related Protein 1 at the Crossroads of Cancer
title_full_unstemmed Dynamin-Related Protein 1 at the Crossroads of Cancer
title_sort Dynamin-Related Protein 1 at the Crossroads of Cancer
author Lima, Ana Rita
author_facet Lima, Ana Rita
Santos, Liliana
Correia, Marcelo
Soares, Paula
Sobrinho-Simões, Manuel
Melo, Miguel
Máximo, Valdemar
author_role author
author2 Santos, Liliana
Correia, Marcelo
Soares, Paula
Sobrinho-Simões, Manuel
Melo, Miguel
Máximo, Valdemar
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Lima, Ana Rita
Santos, Liliana
Correia, Marcelo
Soares, Paula
Sobrinho-Simões, Manuel
Melo, Miguel
Máximo, Valdemar
dc.subject.por.fl_str_mv dynamin-related protein 1
mitochondrial biogenesis
tumorigenesis
cancer
metabolism
topic dynamin-related protein 1
mitochondrial biogenesis
tumorigenesis
cancer
metabolism
description Mitochondrial 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.
publishDate 2018
dc.date.none.fl_str_mv 2018-02-21
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https://hdl.handle.net/10316/107660
https://doi.org/10.3390/genes9020115
url https://hdl.handle.net/10316/107660
https://doi.org/10.3390/genes9020115
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