Single-chain fragment antibody disrupting the EphA4 function as a therapeutic drug for gastric cancer

Studies have shown that the high expression of EphA4 in gastric cancer tissues may correlate with unfavorable clinical pathological characteristics. Therefore, EphA4 may be an effective target for treating gastric cancer in addition to HER-2/neu. In this study, generated scFv S3 can bind endogenous EphA4 of gastric cancer cells and has significant membrane staining. Additionally, scFv S3 binding to EphA4 inhibits the growth and migration of cancer cells and the growth induction that ephrinA1 generates in gastric cancer cells. We found that EphA4 molecules may degrade through antibody treatment of cells, and the increase in LAMP1 and LAMP2 indicates that lysosome is involved in the degradation. The scFv S3 administration leads to the signals pAKT, pERK, and pSTAT3 decrease in cancer cells. The xenograft model of HER-2/neu low expressing gastric cancer cell SNU-16 exhibits better therapeutic effects by scFv S3 than trastuzumab scFv. The scFv S3 administration in vivo can degrade EphA4 molecules in tumor tissues, decreasing Ki67 and increasing cleaved C3 molecule expression. Furthermore, we identified and validated that scFv S3 generates essential ionic bonding with R162 on EphA4. The antibody may provide effective treatment for patients with gastric cancer and abnormal activation or overexpression of EphA4 signaling.

Automated summary

Studies have shown that high expression of EphA4 in gastric cancer tissues is associated with unfavorable clinical pathological characteristics. In this study, the generated scFv S3 was found to bind to endogenous EphA4 in gastric cancer cells, inhibiting the growth and migration of cancer cells. The administration of scFv S3 also resulted in decreased signaling molecules and improved therapeutic effects in a xenograft model. Furthermore, scFv S3 was able to degrade EphA4 molecules in tumor tissues and generate essential ionic bonding with the target protein.