CircRNA_100395 Carried by Exosomes From Adipose-Derived Mesenchymal Stem Cells Inhibits the Malignant Transformation of Non-Small Cell Lung Carcinoma Through the miR-141-3p-LATS2 Axis

The specific purpose of this study is to investigate the impact exosomes from adipose-derived mesenchymal stem cell (AMSC) has on non-small cell lung carcinoma (NSCLC) and the relative applications. circ_100395, miR-141-3p, and LATS2 were expressed and detected in NSCLC and paracancerous tissues as...

Full description

Saved in:
Bibliographic Details
Published in:Frontiers in cell and developmental biology Vol. 9; p. 663147
Main Authors: Zhang, Chong, Cao, Jinlin, Lv, Wang, Mou, Haibo
Format: Journal Article
Language:English
Published: Switzerland Frontiers Media S.A 25-03-2021
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:The specific purpose of this study is to investigate the impact exosomes from adipose-derived mesenchymal stem cell (AMSC) has on non-small cell lung carcinoma (NSCLC) and the relative applications. circ_100395, miR-141-3p, and LATS2 were expressed and detected in NSCLC and paracancerous tissues as well as NSCLC cell lines. Pearson correlation analysis, Dual-Luciferase Reporter Assay and RNA pull-down assay were used to validate their expression and interaction, respectively. After isolation and culture of AMSCs, exosomes were extracted and identified. EdU, epithelial-mesenchymal transition (EMT), and cell colony formation assay were used to distinguish the biological activity of the cells. Expression Hippo/YAP signalling pathway-related proteins were measured by western blotting. Subsequently, tumour volume and weight were confirmed based on xenograft nude mice models, Ki-67 and LATS2 expression was observed by immunohistochemistry. circ_100395 was lowly expressed in NSCLC tissues or cells. The negative correlations and interactions were confirmed between circ_100395 and miR-141-3p, miR-141-3p, and LATS2. AMSC-derived exosomes with overexpression of circ_100395 (exo-circ_100395) significantly inhibited the biological activity as well as EMT of H1650 cells and Hippo/YAP signalling pathway activity. In addition, exo-circ_100395 markedly reduced tumour volume and weight as well as Ki-67 and LASP1 expression . However, overexpressed miR-141-3p or knocked down LATS2 alleviated the above effects. Exo-circ_100395 can increase LATS2 expression by sponging miR-141-3p to regulate Hippo/YAP signalling pathway, thereby inhibiting NSCLC malignant transformation.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Edited by: Shanchun Guo, Xavier University of Louisiana, United States
This article was submitted to Molecular Medicine, a section of the journal Frontiers in Cell and Developmental Biology
Reviewed by: Soichiro Yamamura, University of California, San Francisco, United States; Rilei Jiang, Shanghai University of Traditional Chinese Medicine, China; Fei Hu, Tongji University, China
ISSN:2296-634X
2296-634X
DOI:10.3389/fcell.2021.663147