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miR-29a-3p inhibits endometrial cancer cell proliferation, migration and invasion by targeting VEGFA/CD C42/PAK1.
- Source :
- BMC Cancer; 7/21/2021, Vol. 21 Issue 1, p1-13, 13p
- Publication Year :
- 2021
-
Abstract
- <bold>Background: </bold>This study aimed to investigate the mechanism of miR-29a-3p in regulating endometrial cancer (EC) progression.<bold>Methods: </bold>A total of 72 EC patients were enrolled. EC cells were transfected. Cells proliferation, cloning ability, migration and invasion were researched by MTT assay, colony formation experiment, cell scratch test and Transwell experiment respectively. Dual-luciferase reporter assay was performed. Xenograft experiment was conducted using nude mice. miR-29a-3p, VEGFA, CDC42, PAK1 and p-PAK1 expression in cells/tissues was investigated by qRT-PCR and Western blot.<bold>Results: </bold>miR-29a-3p expression was aberrantly reduced in EC patients, which was associated with poor outcome. miR-29a-3p inhibited EC cells proliferation, cloning formation, migration and invasion (P <  0.05 or P <  0.01 or P <  0.001). miR-29a-3p inhibited CDC42/PAK1 signaling pathway activity in EC cells (P <  0.01). VEGFA expression was directly inhibited by miR-29a-3p. miR-29a-3p suppressed EC cells malignant phenotype in vitro and growth in vivo by targeting VEGFA/CDC42/PAK1 signaling pathway (P < 0.05 or P < 0.01).<bold>Conclusion: </bold>miR-29a-3p inhibits EC cells proliferation, migration and invasion by targeting VEGFA/CDC42/PAK1 signaling pathway. [ABSTRACT FROM AUTHOR]
- Subjects :
- CANCER cell proliferation
ENDOMETRIAL cancer
INHIBITION of cellular proliferation
CANCER cells
CELL proliferation
PROTEIN metabolism
PROTEINS
BIOLOGICAL models
XENOGRAFTS
PHOSPHOTRANSFERASES
RNA
METASTASIS
CELL physiology
CELL motility
TUMOR classification
CELLULAR signal transduction
GENES
ENDOMETRIAL tumors
VASCULAR endothelial growth factors
CELL lines
ANIMALS
MICE
Subjects
Details
- Language :
- English
- ISSN :
- 14712407
- Volume :
- 21
- Issue :
- 1
- Database :
- Complementary Index
- Journal :
- BMC Cancer
- Publication Type :
- Academic Journal
- Accession number :
- 151505796
- Full Text :
- https://doi.org/10.1186/s12885-021-08506-z