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The double face of Morgana in tumorigenesis
Morgana is a chaperone protein able to bind to ROCK I and II and to inhibit their kinase activity. Rho kinases are multifunctional proteins involved in different cellular processes, including cytoskeleton organization, centrosome duplication, cell survival and proliferation. In human cancer samples...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4767456/ https://www.ncbi.nlm.nih.gov/pubmed/26460959 |
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author | Brancaccio, Mara Rocca, Stefania Seclì, Laura Busso, Elena Fusella, Federica |
author_facet | Brancaccio, Mara Rocca, Stefania Seclì, Laura Busso, Elena Fusella, Federica |
author_sort | Brancaccio, Mara |
collection | PubMed |
description | Morgana is a chaperone protein able to bind to ROCK I and II and to inhibit their kinase activity. Rho kinases are multifunctional proteins involved in different cellular processes, including cytoskeleton organization, centrosome duplication, cell survival and proliferation. In human cancer samples Morgana appears to be either downregulated or overexpressed, and experimental evidence indicate that Morgana behaves both as an oncosuppressor and as a proto-oncogene. Our most recent findings demonstrated that if on the one hand low Morgana expression levels, by inducing ROCK II hyperactivation, cause centrosome overduplication and genomic instability, on the other hand, Morgana overexpression induces tumor cell survival and chemoresistance through the ROCK I-PTEN-AKT axis. Therefore, Morgana belongs to a new class of proteins, displaying both oncogenic and oncosuppressor features, depending on the specific cellular context. |
format | Online Article Text |
id | pubmed-4767456 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-47674562016-03-25 The double face of Morgana in tumorigenesis Brancaccio, Mara Rocca, Stefania Seclì, Laura Busso, Elena Fusella, Federica Oncotarget Review Morgana is a chaperone protein able to bind to ROCK I and II and to inhibit their kinase activity. Rho kinases are multifunctional proteins involved in different cellular processes, including cytoskeleton organization, centrosome duplication, cell survival and proliferation. In human cancer samples Morgana appears to be either downregulated or overexpressed, and experimental evidence indicate that Morgana behaves both as an oncosuppressor and as a proto-oncogene. Our most recent findings demonstrated that if on the one hand low Morgana expression levels, by inducing ROCK II hyperactivation, cause centrosome overduplication and genomic instability, on the other hand, Morgana overexpression induces tumor cell survival and chemoresistance through the ROCK I-PTEN-AKT axis. Therefore, Morgana belongs to a new class of proteins, displaying both oncogenic and oncosuppressor features, depending on the specific cellular context. Impact Journals LLC 2015-10-09 /pmc/articles/PMC4767456/ /pubmed/26460959 Text en Copyright: © 2015 Brancaccio et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Review Brancaccio, Mara Rocca, Stefania Seclì, Laura Busso, Elena Fusella, Federica The double face of Morgana in tumorigenesis |
title | The double face of Morgana in tumorigenesis |
title_full | The double face of Morgana in tumorigenesis |
title_fullStr | The double face of Morgana in tumorigenesis |
title_full_unstemmed | The double face of Morgana in tumorigenesis |
title_short | The double face of Morgana in tumorigenesis |
title_sort | double face of morgana in tumorigenesis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4767456/ https://www.ncbi.nlm.nih.gov/pubmed/26460959 |
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