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The Challenges and Opportunities of lncRNAs in Ovarian Cancer Research and Clinical Use

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http://hdl.handle.net/2183/25604
Atribución 4.0 Internacional
Except where otherwise noted, this item's license is described as Atribución 4.0 Internacional
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  • Investigación (FCS) [1293]
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Title
The Challenges and Opportunities of lncRNAs in Ovarian Cancer Research and Clinical Use
Author(s)
Salamini-Montemurri, Martín
Lamas, Mónica
Barreiro-Alonso, Aida
Vizoso-Vázquez, Ángel
Rodríguez-Belmonte, Esther
Quindós-Varela, María
Cerdán, María Esperanza
Date
2020-04-21
Citation
Salamini-Montemurri, M., Lamas-Maceiras, M., Barreiro-Alonso, A., Vizoso-Vázquez, Á., Rodríguez-Belmonte, E., Quindós-Varela, M., & Cerdán, M. E. (2020). The Challenges and Opportunities of LncRNAs in Ovarian Cancer Research and Clinical Use. Cancers, 12(4), 1020. doi:10.3390/cancers12041020
Abstract
[Abstract] Ovarian cancer is one of the most lethal gynecological malignancies worldwide because it tends to be detected late, when the disease has already spread, and prognosis is poor. In this review we aim to highlight the importance of long non-coding RNAs (lncRNAs) in diagnosis, prognosis and treatment choice, to make progress towards increasingly personalized medicine in this malignancy. We review the effects of lncRNAs associated with ovarian cancer in the context of cancer hallmarks. We also discuss the molecular mechanisms by which lncRNAs become involved in cellular physiology; the onset, development and progression of ovarian cancer; and lncRNAs’ regulatory mechanisms at the transcriptional, post-transcriptional and post-translational stages of gene expression. Finally, we compile a series of online resources useful for the study of lncRNAs, especially in the context of ovarian cancer. Future work required in the field is also discussed along with some concluding remarks.
Keywords
Diagnosis
Prognosis
Therapy
Molecular mechanisms
Bioinformatics tools
 
Editor version
https://doi.org/10.3390/cancers12041020
Rights
Atribución 4.0 Internacional
ISSN
2072-6694

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