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Anti-Tumor Activity and Pharmacokinetics of AP25-Fc Fusion Protein. | LitMetric

Anti-Tumor Activity and Pharmacokinetics of AP25-Fc Fusion Protein.

Int J Med Sci

Department of Biochemistry and Molecular Biology, The State Key Laboratory of Cancer Biology, The Fourth Military Medical University, Xi'an 710032, China.

Published: February 2020

AI Article Synopsis

  • AP25 is an anti-tumor peptide that inhibits both angiogenesis and tumor cell growth but has a short half-life of 50 minutes, limiting its potential use.
  • Researchers created fusion proteins of AP25 and IgG4 Fc to extend its half-life while maintaining its effectiveness.
  • The selected fusion protein, PSG4R, demonstrated significant anti-tumor effects against human colon cancer in mouse models, with a much longer half-life of about 56 hours, highlighting its promise for future drug development.

Article Abstract

AP25 is an anti-tumor peptide with a high affinity for integrins. It exerts its anti-tumor activity by inhibiting angiogenesis and by directly inhibiting the growth of tumor cells. Its half-life time is only about 50 minutes, which limits its clinical application. In order to prolong the half-life time of AP25 while preserving its anti-tumor activity, several fusion proteins of AP25 and IgG4 Fc were designed and expressed; their anti-tumor activity and pharmacokinetics properties were evaluated. Firstly, four AP25-Fc fusion protein sequences were designed, and the corresponding proteins were expressed and purified. Based on the results of HUVEC migration inhibition assay, HUVEC and tumor cell proliferation inhibition assay and yields of expression by HEK293 cells, the fusion protein designated PSG4R was selected for further evaluation. The anti-tumor effect of PSG4R was then evaluated on HCT-116 nude mice xenograft model. And the pharmacokinetics properties of PSG4R were investigated in rats. The results showed that PSG4R could inhibit the growth of xenografts of human colon cancer cell line HCT-116 in nude mice by intravenous administration of 40 mg/kg once every two days. The half-life time of PSG4R was 56.270 ± 15.398 h. This study showed that the construction of AP25-Fc fusion protein could significantly prolong the half-life of AP25 while retaining its anti-tumor activity, which provides a new direction for new drug development of AP25.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6643120PMC
http://dx.doi.org/10.7150/ijms.34365DOI Listing

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