MiR-7 promotes epithelial cell transformation by targeting the tumor suppressor KLF4


Por: Meza-Sosa, KF, Perez-Garcia, EI, Camacho-Concha, N, Lopez-Gutierrez, O, Pedraza-Alva, G, Perez-Martinez, L

Publicada: 2 sep 2014
Resumen:
MicroRNAs (miRNAs) are endogenous small non-coding RNAs that have a pivotal role in the post-transcriptional regulation of gene expression and their misregulation is common in different types of cancer. Although it has been shown that miR-7 plays an oncogenic role in different cellular contexts, the molecular mechanisms by which miR-7 promotes cell transformation are not well understood. Here we show that the transcription factor KLF4 is a direct target of miR-7 and present experimental evidence indicating that the regulation of KLF4 by miR-7 has functional implications in epithelial cell transformation. Stable overexpression of miR-7 into lung and skin epithelial cells enhanced cell proliferation, cell migration and tumor formation. Alteration of these cellular functions by miR-7 resulted from misregulation of KLF4 target genes involved in cell cycle control. miR-7-induced tumors showed decreased p21 and increased Cyclin D levels. Taken together, these findings indicate that miR-7 acts as an oncomiR in epithelial cells in part by directly regulating KLF4 expression. Thus, we conclude that miR-7 acts as an oncomiR in the epithelial cellular context, where through the negative regulation of KLF4-dependent signaling pathways, miR-7 promotes cellular transformation and tumor growth. © 2014 Meza-Sosa et al.

Filiaciones:
Meza-Sosa, KF:
 Univ Nacl Autonoma Mexico, Inst Biotecnol, Dept Med Mol & Bioproc, Lab Neuroinmunobiol, Cuernavaca 62191, Morelos, Mexico

Perez-Garcia, EI:
 Univ Nacl Autonoma Mexico, Inst Biotecnol, Dept Med Mol & Bioproc, Lab Neuroinmunobiol, Cuernavaca 62191, Morelos, Mexico

Camacho-Concha, N:
 Univ Nacl Autonoma Mexico, Inst Biotecnol, Dept Med Mol & Bioproc, Lab Neuroinmunobiol, Cuernavaca 62191, Morelos, Mexico

Lopez-Gutierrez, O:
 Univ Nacl Autonoma Mexico, Inst Biotecnol, Dept Med Mol & Bioproc, Lab Neuroinmunobiol, Cuernavaca 62191, Morelos, Mexico

Pedraza-Alva, G:
 Univ Nacl Autonoma Mexico, Inst Biotecnol, Dept Med Mol & Bioproc, Lab Neuroinmunobiol, Cuernavaca 62191, Morelos, Mexico

Perez-Martinez, L:
 Univ Nacl Autonoma Mexico, Inst Biotecnol, Dept Med Mol & Bioproc, Lab Neuroinmunobiol, Cuernavaca 62191, Morelos, Mexico
ISSN: 19326203
Editorial
PUBLIC LIBRARY SCIENCE, 1160 BATTERY STREET, STE 100, SAN FRANCISCO, CA 94111 USA, Estados Unidos America
Tipo de documento: Article
Volumen: 9 Número: 9
Páginas:
WOS Id: 000341231500007
ID de PubMed: 25181544