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Authordc.contributor.authorRetamales-Ortega, Rocío 
Authordc.contributor.authorOróstica Arévalo, María Lorena 
Authordc.contributor.authorVera, Carolina 
Authordc.contributor.authorCuevas, Paula 
Authordc.contributor.authorHernández, Andrea 
Authordc.contributor.authorHurtado, Iván 
Authordc.contributor.authorVega Blanco, María Margarita 
Authordc.contributor.authorRomero Osses, Carmen 
Admission datedc.date.accessioned2019-03-18T11:56:26Z
Available datedc.date.available2019-03-18T11:56:26Z
Publication datedc.date.issued2017
Cita de ítemdc.identifier.citationInternational Journal of Molecular Sciences, Volumen 18, Issue 3, 2018,
Identifierdc.identifier.issn14220067
Identifierdc.identifier.issn16616596
Identifierdc.identifier.other10.3390/ijms18030507
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/167115
Abstractdc.description.abstract© 2017 by the authors. Licensee MDPI, Basel, Switzerland. Ovarian cancer is the eighth most common cancer in women worldwide, and epithelial ovarian cancer (EOC) represents 90% of cases. Nerve growth factor (NGF) and its high affinity receptor tyrosine kinase A receptor (TRKA) have been associated with the development of several types of cancer, including EOC; both NGF and TRKA levels are elevated in this pathology. EOC presents high angiogenesis and several molecules have been reported to induce this process. NGF increases angiogenesis through its TRKA receptor on endothelial cells, and by indirectly inducing vascular endothelial growth factor expression. Other molecules controlled by NGF include ciclooxigenase-2, disintegrin and metalloproteinase domain-containing protein 17 (ADAM17) and calreticulin (CRT), proteins involved in crucial processes needed for EOC progression. These molecules could be modified through microRNA regulation, which could be regulated by NGF. MicroRNAs are th
Lenguagedc.language.isoen
Publisherdc.publisherMDPI AG
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourceInternational Journal of Molecular Sciences
Keywordsdc.subjectEpithelial ovarian cancer
Keywordsdc.subjectmicroRNAs
Keywordsdc.subjectNerve growth factor (NGF)
Keywordsdc.subjectNeurotrophins
Keywordsdc.subjectTyrosine kinase A receptor (TRKA)
Títulodc.titleRole of nerve growth factor (NGF) and miRNAs in epithelial ovarian cancer
Document typedc.typeArtículo de revista
dcterms.accessRightsdcterms.accessRightsAcceso Abierto
Catalogueruchile.catalogadorSCOPUS
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile