MicroRNA‑34a inhibits esophageal squamous cell carcinoma progression by targeting E2F5.
Apoptosis
Biomarkers, Tumor
/ genetics
Cell Proliferation
Disease Progression
E2F5 Transcription Factor
/ genetics
Esophageal Neoplasms
/ genetics
Esophageal Squamous Cell Carcinoma
/ genetics
Gene Expression Regulation, Neoplastic
Humans
MicroRNAs
/ genetics
Prognosis
Survival Rate
Tumor Cells, Cultured
Journal
Journal of B.U.ON. : official journal of the Balkan Union of Oncology
ISSN: 2241-6293
Titre abrégé: J BUON
Pays: Cyprus
ID NLM: 100883428
Informations de publication
Date de publication:
Historique:
entrez:
27
1
2020
pubmed:
27
1
2020
medline:
20
6
2020
Statut:
ppublish
Résumé
Previous studies have explored the role of microRNA-34a (miR-34a) and E2F transcription family in several tumors, however, the expression level and oncogenesis mechanism of these two factors in esophageal squamous cancer cells (ESCC) remains unclear. Our study aims to explore the inhibitory effect of miR-34a in ESCC as well as its downstream factor E2F5. We explored the relevant expression level of miR-34a in human tumor tissue as well as in several ESCC cell lines. Through RNA mimic and inhibitor, we examined the specific role of miR-34a in the proliferation, apoptosis and migration of tumor cells, and we further explored the role of downstream factor E2F5 through gain- and loss-of-function analyses. We found that the expression level of miR-34a is significantly downregulated in ESCC tissues as well as in ESCC cell lines, and miR-34a plays an inhibitory role in tumor cell proliferation and migration while it promotes tumor cell apoptosis. We further showed that E2F5 is a direct functional target of miR-34a, as it promotes tumor cell proliferation and migration and inhibits apoptosis. Our results indicate that the intrinsic expression of miR-34a was relatively low in ESCC. The anti-tumor effect of miR-34a is possibly dependent on the regulation of cell-cycle regulator E2F5.
Substances chimiques
Biomarkers, Tumor
0
E2F5 Transcription Factor
0
E2F5 protein, human
0
MIRN34 microRNA, human
0
MicroRNAs
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM