Abstract

Lymph node metastasis (LNM) is a common invasive feature of hepatocellular carcinoma (HCC) associated with poor clinical outcomes. Through microarray profiling and bioinformatic analyses, we identified the circ-0044539-miR-29a-3p-VEGFA axis as a potential key factor in the progression of HCC LNM. In HCC cells and nude mice, circ-0044539 downregulation or miR-29a-3p upregulation was associated with small tumor size, PI3K-AKT-mTOR pathway inactivation, and downregulation of the key LNM factors (HIF-1α and CXCR4). Furthermore, circ-0044539 was also responsible for exosomal miR-29a-3p secretion. Exosomal miR-29a-3p was then observed to migrate to the LNs and downregulate High-mobility group box transcription factor 1 (Hbp1) in Polymorphonuclear Myeloid-derived suppressor cells (PMN-MDSCs), inducing the formation of a microenvironment suitable for tumor colonization. Overall, circ-0044539 promotes HCC cell LNM abilities and induces an immune-suppressive environment in LNs through exosomes, highlighting its potential as a target for HCC LNM and HCC immunotherapy.

Details

Title
Circ-0044539 promotes lymph node metastasis of hepatocellular carcinoma through exosomal-miR-29a-3p
Author
Yang, Yi 1   VIAFID ORCID Logo  ; Chen, Xue-Qin 1 ; Jia, Ya-Xun 1 ; Ma, Jie 1   VIAFID ORCID Logo  ; Xu, Di 1 ; Xiang, Zuo-Lin 2   VIAFID ORCID Logo 

 Tongji University, Department of Radiation Oncology, Shanghai East Hospital, School of Medicine, Shanghai, China (GRID:grid.24516.34) (ISNI:0000000123704535) 
 Tongji University, Department of Radiation Oncology, Shanghai East Hospital, School of Medicine, Shanghai, China (GRID:grid.24516.34) (ISNI:0000000123704535); Shanghai East Hospital Ji’an hospital, Department of Radiation Oncology, Ji’an City, China (GRID:grid.452753.2) (ISNI:0000 0004 1799 2798) 
Pages
630
Publication year
2024
Publication date
Aug 2024
Publisher
Springer Nature B.V.
e-ISSN
20414889
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
3097624388
Copyright
© The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.