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Preparation and Characterization of Anti-GPC3 Nanobody Against Hepatocellular Carcinoma. | LitMetric

Preparation and Characterization of Anti-GPC3 Nanobody Against Hepatocellular Carcinoma.

Int J Nanomedicine

Xinjiang Key Laboratory of Biological Resources and Genetic Engineering, College of Life Science and Technology, Xinjiang University, Urumqi 830046, People's Republic of China.

Published: June 2020

AI Article Synopsis

Article Abstract

Background: Glypican-3 (GPC3) is a newly identified target molecule for the early diagnosis of hepatocellular carcinoma (HCC), while targeted inhibition of GPC3 signaling may help to control the proliferation and metastasis of HCC cells. The purpose of this study was to prepare the anti-GPC3 nanobody and to investigate the affinity of the anti-GPC3 nanobodies in vitro and the anticancer effects on hepatocellular carcinoma in vivo.

Methods: To screen for unknown anti-GPC3 antibodies, we constructed an antibody phage display library. After three rounds of panning, positive phage clones were identified by enzyme-linked immunosorbent assay (ELISA). Further, the nanobody fusion protein was expressed in BL21 cells and purified by affinity chromatography. Competitive ELISA and flow cytometry were conducted to confirm the affinity of the anti-GPC3 nanobodies in vitro. The antitumor effects of VHH were assessed in vivo.

Results: The results showed that the nanobody VHH had specific high-affinity binding to His-GPC3 antigen. Moreover, VHH exhibited specific binding to commercial human GPC3 and recognized the surface GPC3 protein of the hepatoma cell line HepG2. Importantly, in vivo study showed that GPC3 nanobody suppresses the growth of HepG2 and improves the survival rate of tumor mice.

Discussion: In summary, our new anti-GPC3 nanobody suggests a strong application potential for targeted therapy of liver cancer.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125335PMC
http://dx.doi.org/10.2147/IJN.S235058DOI Listing

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