Skip navigation
  •  Inicio
  • UDC 
    • Cómo depositar
    • Políticas del RUC
    • FAQ
    • Derechos de autor
    • Más información en INFOguías UDC
  • Listar 
    • Comunidades
    • Buscar por:
    • Fecha de publicación
    • Autor
    • Título
    • Materia
  • Ayuda
    • español
    • Gallegan
    • English
  • Acceder
  •  Español 
    • Español
    • Galego
    • English
  
Ver ítem 
  •   RUC
  • Facultade de Ciencias da Saúde
  • Investigación (FCS)
  • Ver ítem
  •   RUC
  • Facultade de Ciencias da Saúde
  • Investigación (FCS)
  • Ver ítem
JavaScript is disabled for your browser. Some features of this site may not work without it.

Identification of lncRNAs Deregulated in Epithelial Ovarian Cancer Based on a Gene Expression Profiling Meta-Analysis

Thumbnail
Ver/Abrir
Cerdan_MariaEsperanza_2023_Identification_lncRNAs_deregulated_epithelial_ovarian_cancer.pdf (8.931Mb)
Use este enlace para citar
http://hdl.handle.net/2183/39973
Atribución 4.0 Internacional
Excepto si se señala otra cosa, la licencia del ítem se describe como Atribución 4.0 Internacional
Colecciones
  • Investigación (FCS) [1293]
Metadatos
Mostrar el registro completo del ítem
Título
Identification of lncRNAs Deregulated in Epithelial Ovarian Cancer Based on a Gene Expression Profiling Meta-Analysis
Autor(es)
Salamini-Montemurri, Martín
Lamas, Mónica
Lorenzo-Catoira, Lidia
Vizoso-Vázquez, Ángel
Barreiro-Alonso, Aida
Rodríguez-Belmonte, Esther
Quindós-Varela, María
Cerdán, María Esperanza
Fecha
2023-06-28
Cita bibliográfica
Salamini-Montemurri, M.; Lamas-Maceiras, M.; Lorenzo-Catoira, L.; Vizoso-Vázquez, Á.; Barreiro-Alonso, A.; Rodríguez-Belmonte, E.; Quindós-Varela, M.; Cerdán, M.E. Identification of lncRNAs Deregulated in Epithelial Ovarian Cancer Based on a Gene Expression Profiling Meta-Analysis. Int. J. Mol. Sci. 2023, 24, 10798. https://doi.org/10.3390/ijms241310798
Resumen
[Abstract] Epithelial ovarian cancer (EOC) is one of the deadliest gynecological cancers worldwide, mainly because of its initially asymptomatic nature and consequently late diagnosis. Long non-coding RNAs (lncRNA) are non-coding transcripts of more than 200 nucleotides, whose deregulation is involved in pathologies such as EOC, and are therefore envisaged as future biomarkers. We present a meta-analysis of available gene expression profiling (microarray and RNA sequencing) studies from EOC patients to identify lncRNA genes with diagnostic and prognostic value. In this meta-analysis, we include 46 independent cohorts, along with available expression profiling data from EOC cell lines. Differential expression analyses were conducted to identify those lncRNAs that are deregulated in (i) EOC versus healthy ovary tissue, (ii) unfavorable versus more favorable prognosis, (iii) metastatic versus primary tumors, (iv) chemoresistant versus chemosensitive EOC, and (v) correlation to specific histological subtypes of EOC. From the results of this meta-analysis, we established a panel of lncRNAs that are highly correlated with EOC. The panel includes several lncRNAs that are already known and even functionally characterized in EOC, but also lncRNAs that have not been previously correlated with this cancer, and which are discussed in relation to their putative role in EOC and their potential use as clinically relevant tools.
Palabras clave
Long non-coding RNAs (lncRNAs)
Epithelial ovarian cancer (EOC)
Transcriptomics
Meta-analysis
 
Descripción
This article belongs to the Special Issue Non-coding RNAs' Functionality-Diagnosis and Therapy in Cancer and Other Indications
Versión del editor
https://doi.org/10.3390/ijms241310798
Derechos
Atribución 4.0 Internacional
ISSN
1422-0067

Listar

Todo RUCComunidades & ColeccionesPor fecha de publicaciónAutoresTítulosMateriasGrupo de InvestigaciónTitulaciónEsta colecciónPor fecha de publicaciónAutoresTítulosMateriasGrupo de InvestigaciónTitulación

Mi cuenta

AccederRegistro

Estadísticas

Ver Estadísticas de uso
Sherpa
OpenArchives
OAIster
Scholar Google
UNIVERSIDADE DA CORUÑA. Servizo de Biblioteca.    DSpace Software Copyright © 2002-2013 Duraspace - Sugerencias