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The versatile nature of miR-9/9(*) in human cancer

miR-9 and miR-9(*) (miR-9/9(*)) were first shown to be expressed in the nervous system and to function as versatile regulators of neurogenesis. The variable expression levels of miR-9/9(*) in human cancer prompted researchers to investigate whether these small RNAs may also have an important role in...

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Detalles Bibliográficos
Autores principales: Nowek, Katarzyna, Wiemer, Erik A.C., Jongen-Lavrencic, Mojca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5945517/
https://www.ncbi.nlm.nih.gov/pubmed/29755694
http://dx.doi.org/10.18632/oncotarget.24889
Descripción
Sumario:miR-9 and miR-9(*) (miR-9/9(*)) were first shown to be expressed in the nervous system and to function as versatile regulators of neurogenesis. The variable expression levels of miR-9/9(*) in human cancer prompted researchers to investigate whether these small RNAs may also have an important role in the deregulation of physiological and biochemical networks in human disease. In this review, we present a comprehensive overview of the involvement of miR-9/9(*) in various human malignancies focusing on their opposing roles in supporting or suppressing tumor development and metastasis. Importantly, it is shown that the capacity of miR-9/9(*) to impact tumor formation is independent from their influence on the metastatic potential of tumor cells. Moreover, data suggest that miR-9/9(*) may increase malignancy of one cancer cell population at the expense of another. The functional versatility of miR-9/9(*) emphasizes the complexity of studying miRNA function and the importance to perform functional studies of both miRNA strands in a relevant cellular context. The possible application of miR-9/9(*) as targets for miRNA-based therapies is discussed, emphasizing the need to obtain a better understanding of the functional properties of these miRNAs and to develop safe delivery methods to target specific cell populations.