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MicroRNAs as novel epigenetic biomarkers for human cancer
Cortés-Sempere, M; Ibáñez de Cáceres, I.
Afiliación
  • Cortés-Sempere, M; Instituto de Investigaciones Biomédicas CSIC/UAM. IdiPAZ. Madrid. Spain
  • Ibáñez de Cáceres, I; University Hospital La Paz. Madrid. Spain
Clin. transl. oncol. (Print) ; 13(6): 357-362, jun. 2011. tab, ilus
Article en En | IBECS | ID: ibc-124674
Biblioteca responsable: ES1.1
Ubicación: BNCS
ABSTRACT
MicroRNAs (miRNAs) are regulatory, non-coding RNAs that are approximately 22 nucleotides in length. Nearly 1000 unique miRNAs encoded in the human genome have been identified, shedding new light on the posttranscriptional regulation of more than one-third of human genes. These miRNAs are involved in numerous biological processes, including development, differentiation, apoptosis, homeostasis and stem cell biology. Aberrant miRNA expression patterns also play a substantial role in carcinogenesis. It is believed that genetic and epigenetic regulation is responsible for changes in miRNA expression in cancer development, however the exact mechanisms remain unclear. miRNAs are involved in almost all aspects of cancer biology such as apoptosis, invasion, metastasis and angiogenesis. Thanks to this wide range of biological functions, the analysis of changes in overall miRNA expression occurring within human tumours has helped identify miRNA signatures associated with diagnosis, staging, progression, prognosis and response to treatment. This positions miRNA- targeting therapeutics as a novel and promising tool for cancer treatment (AU)
Asunto(s)
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Colección: 06-national / ES Base de datos: IBECS Asunto principal: Neoplasias de la Mama / Biomarcadores de Tumor / MicroARNs / Epigenómica Tipo de estudio: Prognostic_studies Límite: Humans / Male Idioma: En Revista: Clin. transl. oncol. (Print) Año: 2011 Tipo del documento: Article
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Colección: 06-national / ES Base de datos: IBECS Asunto principal: Neoplasias de la Mama / Biomarcadores de Tumor / MicroARNs / Epigenómica Tipo de estudio: Prognostic_studies Límite: Humans / Male Idioma: En Revista: Clin. transl. oncol. (Print) Año: 2011 Tipo del documento: Article