CLONING OF A CANCER CELL–PRODUCING HEPATOCYTE GROWTH FACTOR, VASCULAR ENDOTHELIAL GROWTH FACTOR, AND INTERLEUKIN-8 FROM GASTRIC CANCER CELLS

Author(s):  
MINEKO IWAI ◽  
MASAHIKO MATSUDA ◽  
YOSHIAKI IWAI
2020 ◽  
Vol 53 (1) ◽  
Author(s):  
Miao Liu ◽  
Wanfu Xu ◽  
Mingmin Su ◽  
Pingsheng Fan

Abstract Background Tumor angiogenesis is an essential event for tumor growth and metastasis. It has been showed that REC8, a component of the meiotic cohesion complex, played a vital role in Epithelial-Mesenchymal Transition (EMT) in gastric cancer. However, the role of REC8 in gastric cancer angiogenesis remains to be identified. Results Inhibition of REC8 expression in gastric cancer cells contributed to tumor angiogenesis in the gastric cancer microenvironment. The clinical analysis demonstrated that the loss of REC8 in gastric cancer with enrichment of MVD. Depletion of REC8 expression in gastric cancer cells significantly increased tube formation of human umbilical vein endothelial cells (HUVECs), which is attributed to enhancement of vascular endothelial growth factor (VEGF) secretion caused by REC8 slicing. While addition of neutralizing antibody targeted VEGF into supernatant drastically reversed the effect of REC8 loss in gastric cancer cells on tube formation. Mechanistic analyses indicated that ablation of REC8 promotes nuclear factor-κB (NF-κB) p65 activity and its downstream gene VEGF expression, leading to tube formation. Conclusions These results demonstrated a novel REC8 function that suppressed tumor angiogenesis and progression by attenuation of VEGF in gastric cancer microenvironment.


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