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Effect of microrna-138 on epithelial-Mesenchymal transition and invasion of breast cancer cells by targeting semaphorin 4C
- Source :
- Bioengineered, article-version (VoR) Version of Record, Bioengineered, Vol 12, Iss 2, Pp 10117-10125 (2021)
- Publication Year :
- 2021
-
Abstract
- In view of the role of miR-138 in cancer cells, we predicted the target of miR-138 and its targeting to SEMA4C by bioinformatics software and luciferase experiment. The expression levels of miR-138 in human normal breast epithelial cells and two kinds of BC cells were compared, and the transfection cells were selected. MiR-138 mimetic negative control (miR-NC), miR-138 mimic and miR-138 inhibitor were designed for cell transfection. The results showed that the expression level of miR-138 in MCF-7 cells was the lowest. The up regulation of miR-138 would lead to the high expression of E-cad and the low expression of N-cad, vim and SEMA4C, and the vitality and invasion of BC cells would decrease. The down regulation of miR-138 would lead to the low expression of E-cad and the high expression of N-cad, vim and SEMA4C, and the vitality and invasion of BC cells would increase. miR-138 targeted regulation of SEMA4C can promote the expression of N-cad, inhibit the expression of E-cad, vim and SEMA4C, reverse the EMT of BC cells, and inhibit the activity and invasion of BC cells. MiR-138 has clinical potential as a tumor marker of BC.
- Subjects :
- Epithelial-Mesenchymal Transition
Cell Survival
semaphorin 4C
epithelial mesenchymal transition
miR-138
Bioengineering
Breast Neoplasms
Semaphorins
Biology
Applied Microbiology and Biotechnology
Breast cancer
Downregulation and upregulation
Cell Line, Tumor
microRNA
Humans
Luciferase
Neoplasm Invasiveness
Epithelial–mesenchymal transition
Tumor marker
Cell Proliferation
Binding Sites
Base Sequence
General Medicine
Transfection
invasion
Gene Expression Regulation, Neoplastic
MicroRNAs
Cancer cell
Cancer research
Female
TP248.13-248.65
Biotechnology
Research Article
Research Paper
Subjects
Details
- ISSN :
- 21655987
- Volume :
- 12
- Issue :
- 2
- Database :
- OpenAIRE
- Journal :
- Bioengineered
- Accession number :
- edsair.doi.dedup.....1d5a7a4687cc9cee11aaa2bd8f6afa6d