Transcribed Ultraconserved Regions: New regulators in cancer signaling and potential biomarkers



Título del documento: Transcribed Ultraconserved Regions: New regulators in cancer signaling and potential biomarkers
Revue: Genetics and molecular biology
Base de datos: PERIÓDICA
Número de sistema: 000459161
ISSN: 1415-4757
Autores: 1
Instituciones: 1Universidade Federal do Parana, Departamento de Genetica, Curitiba, Parana. Brasil
Año:
Volumen: 46
Número: 1
País: Brasil
Idioma: Inglés
Tipo de documento: Artículo
Enfoque: Descriptivo
Resumen en inglés The ultraconserved regions (UCRs) are 481 genomic elements, longer than 200 bp, 100% conserved in human, mouse, and rat genomes. Usually, coding regions are more conserved, but more than 80% of UCRs are either intergenic or intronic, and many of them produce long non-coding RNAs (lncRNAs). Recently, the deregulated expression of transcribed UCRs (T-UCRs) has been associated with pathological conditions. But, differently from many lncRNAs with recognized crucial effects on malignant cell processes, the role of T-UCRs in the control of cancer cell networks is understudied. Furthermore, the potential utility of these molecules as molecular markers is not clear. Based on this information, the present review aims to organize information about T-UCRs with either oncogenic or tumor suppressor role associated with cancer cell signaling, and better describe T-UCRs with potential utility as prognosis markers. Out of 481 T-UCRs, 297 present differential expression in cancer samples, 23 molecules are associated with tumorigenesis processes, and 12 have more clear potential utility as prognosis markers. In conclusion, T-UCRs are deregulated in several tumor types, highlighted as important molecules in cancer networks, and with potential utility as prognosis markers, although further investigation for translational medicine is still needed
Disciplinas: Medicina
Palabras clave: Oncología,
Apoptosis,
Transcripción,
Metástasis,
Cáncer,
Biomarcadores,
Revisión bibliográfica
Keyword: Oncology,
Apoptosis,
Transcription,
Cancer,
Biomarkers,
Metastasis,
Bibliographic review
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