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miR-10b expression in breast cancer stem cells supports self-renewal through negative PTEN regulation and sustained AKT activation.
Bahena-Ocampo, Ivan; Espinosa, Magali; Ceballos-Cancino, Gisela; Lizarraga, Floria; Campos-Arroyo, Denise; Schwarz, Angela; Maldonado, Vilma; Melendez-Zajgla, Jorge; Garcia­Lopez, Patricia.
Afiliação
  • Bahena-Ocampo I; Basic Research Subdivision, National Institute of Genomic Medicine, Functional Genomics Laboratory, Mexico City, Mexico.
  • Espinosa M; Basic Research Subdivision, National Institute of Genomic Medicine, Functional Genomics Laboratory, Mexico City, Mexico.
  • Ceballos-Cancino G; Basic Research Subdivision, National Institute of Genomic Medicine, Functional Genomics Laboratory, Mexico City, Mexico.
  • Lizarraga F; Basic Research Subdivision, National Institute of Genomic Medicine, Functional Genomics Laboratory, Mexico City, Mexico.
  • Campos-Arroyo D; Basic Research Subdivision, National Institute of Genomic Medicine, Functional Genomics Laboratory, Mexico City, Mexico.
  • Schwarz A; Basic Research Subdivision, National Institute of Genomic Medicine, Functional Genomics Laboratory, Mexico City, Mexico.
  • Maldonado V; Basic Research Subdivision, National Institute of Genomic Medicine, Functional Genomics Laboratory, Mexico City, Mexico.
  • Melendez-Zajgla J; Basic Research Subdivision, National Institute of Genomic Medicine, Functional Genomics Laboratory, Mexico City, Mexico jmelendez@inmegen.gob.mx.
  • Garcia­Lopez P; Basic Research Subdivision, National Institute of Genomic Medicine, Functional Genomics Laboratory, Mexico City, Mexico jmelendez@inmegen.gob.mx.
EMBO Rep ; 17(5): 648-58, 2016 05.
Article em En | MEDLINE | ID: mdl-27113763
Cancer stem cells (CSCs) are linked to metastasis. Moreover, a discrete group of miRNAs (metastamiRs) has been shown to promote metastasis. Accordingly, we propose that miRNAs that function as metastatic promoters may influence the CSC phenotype. To study this issue, we compared the expression of 353 miRNAs in CSCs enriched from breast cancer cell lines using qRT-PCR analysis. One of the most altered miRNAs was miR-10b, which is a reported promoter of metastasis and migration. Stable overexpression of miR-10b in MCF-7 cells (miR-10b-OE cells) promoted higher self-renewal and expression of stemness and epithelial-mesenchymal transition (EMT) markers. In agreement with these results, inhibiting miR-10b expression using synthetic antisense RNAs resulted in a decrease in CSCs self-renewal. Bioinformatics analyses identified several potential miR-10b mRNA targets, including phosphatase and tensin homolog (PTEN), a key regulator of the PI3K/AKT pathway involved in metastasis, cell survival, and self-renewal. The targeting of PTEN by miR-10b was confirmed using a luciferase reporter, qRT-PCR, and Western blot analyses. Lower PTEN levels were observed in CSCs, and miR-10b depletion not only increased PTEN mRNA and protein expression but also decreased the activity of AKT, a downstream PTEN target kinase. Correspondingly, PTEN knockdown increased stem cell markers, whereas AKT inhibitors compromised the self-renewal ability of CSCs and breast cancer cell lines overexpressing miR-10b. In conclusion, miR-10b regulates the self-renewal of the breast CSC phenotype by inhibiting PTEN and maintaining AKT pathway activation.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células-Tronco Neoplásicas / Neoplasias da Mama / MicroRNAs / PTEN Fosfo-Hidrolase / Proteínas Proto-Oncogênicas c-akt / Autorrenovação Celular Limite: Animals / Female / Humans Idioma: En Revista: EMBO Rep Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2016 Tipo de documento: Article País de afiliação: México País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células-Tronco Neoplásicas / Neoplasias da Mama / MicroRNAs / PTEN Fosfo-Hidrolase / Proteínas Proto-Oncogênicas c-akt / Autorrenovação Celular Limite: Animals / Female / Humans Idioma: En Revista: EMBO Rep Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2016 Tipo de documento: Article País de afiliação: México País de publicação: Reino Unido