miR-4677-3p participates proliferation and metastases of gastric cancer cell via CEMIP-PI3K/AKT signaling pathway

Gastric cancer is one of the top three leading causes of cancer-related death in the world. Evidence indicated that miR-4677-3p was dysregulated and involved in modulating invasion and migration in multiple types of cancer cells. The aim of this research is to explore the function and mechanism of miR-4677-3p in the development of gastric cancer. In this study, we discovered that miR-4677-3p was down-regulated in gastric cancer tissues and cells. Over-expression of miR-4677-3p suppressed the proliferation, migration and invasion of gastric cancer cells. Furthermore, miR-4677-3p directly bond to CEMIP 3'UTR region and inhibited CEMIP expression. CEMIP promoted cell proliferation, migration and invasion of gastric cancer cells via accelerating PI3K/AKT signaling pathway. siCEMIP or PI3K/AKT signaling inhibitor (Akti-1/2 and LY294002) partly reversed the effects of miR-4677-3p on the cellular growth and metastasis of gastric cancer. In general, miR-4677-3p regulated the development of gastric cancer through CEMIP-PI3K/AKT signaling pathway axis. This study verified the function and molecular mechanism of miR-4677-3p in gastric cancer cells, and may provide a potential diagnosis/prognosis target for patients with gastric cancer.

Medienart:

E-Artikel

Erscheinungsjahr:

2021

Erschienen:

2021

Enthalten in:

Zur Gesamtaufnahme - volume:20

Enthalten in:

Cell cycle (Georgetown, Tex.) - 20(2021), 19 vom: 27. Okt., Seite 1978-1987

Sprache:

Englisch

Beteiligte Personen:

Mi, Chen [VerfasserIn]
Zhang, Dan [VerfasserIn]
Li, Yarui [VerfasserIn]
Ren, Mudan [VerfasserIn]
Ma, Wenhui [VerfasserIn]
Lu, Guifang [VerfasserIn]
He, Shuixiang [VerfasserIn]

Links:

Volltext

Themen:

EC 2.7.11.1
Gastric cancer
Journal Article
MIRN4697 microRNA, human
Metastases
MiR-4677-3p
MicroRNAs
Proto-Oncogene Proteins c-akt
Research Support, Non-U.S. Gov't

Anmerkungen:

Date Completed 07.04.2022

Date Revised 27.08.2022

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1080/15384101.2021.1971375

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM329807331