THBS4/integrin α2 axis mediates BM-MSCs to promote angiogenesis in gastric cancer associated with chronic infection.

BACKGROUND

BM-MSCs contribute to -induced gastric cancer, but their mechanism is still unclear. The aim of our study was to investigate the specific role and mechanism of BM-MSCs in -induced gastric cancer.

MAIN METHODS

Mice received total bone marrow transplants and were then infected with . BM-MSCs were extracted and transplanted into the gastric serosal layer of mice chronically infected with . Hematoxylin and eosin staining, immunohistochemistry staining and immunofluorescence were performed to detect tumor growth and angiogenesis in mouse stomach tissues. Chicken chorioallantoic membrane assays, xenograft tumor models, and human umbilical vein endothelial cell tube formation assays were used for and angiogenesis studies. THBS4 was screened from RNA-seq analysis of gastric tissues of BM-MSCs transplanted into infected mice.

RESULTS

BM-MSCs can migrate to the site of chronic mucosal injury and promote tumor angiogenesis associated with chronic infection. Migration of BM-MSCs to the site of chronic mucosal injury induced the upregulation of THBS4, which was also evident in human gastric cancer and correlated with increased blood vessel formation and worse outcome. The THBS4/integrin α2 axis promoted angiogenesis by facilitating the PI3K/AKT pathway in endothelial cells.

CONCLUSIONS

Our results revealed a novel proangiogenic effect of BM-MSCs in the chronic infection microenvironment, primarily mediated by the THBS4/integrin α2 axis, which activates the PI3K/AKT pathway in endothelial cells and eventually induces the formation of new tumor vessels.