Anticancer Therapy by Tumor Vessel Infarction with Polyethylene Glycol Conjugated Retargeted Tissue Factor

作者：Schwoeppe Christian; Zerbst Caroline; Froehlich Max; Schliemann Christoph; Kessler Torsten; Liersch Ruediger; Overkamp Laura; Holtmeier Richard; Stypmann Joerg; Dreiling Alena; Koenig Simone; Hoeltke Carsten; Luecke Martin; Mueller Tidow Carsten; Mesters Rolf M; Berdel Wolfgang E^*

来源：Journal of Medicinal Chemistry, 2013, 56(6): 2337-2347.

DOI：10.1021/jm301669z

TF-NGR consists of the extracellular domain of tissue factor and the peptide GNGRAHA, a ligand of the surface protein aminopeptidase N and of integrin alpha(v)beta(3). Both surface proteins are upregulated on endothelial cells of tumor vessels. tTF-NGR shows antitumor activity in xenografts and inhibition of tumor blood flow in cancer patients. We performed random TMS(PEG)(12) PEGylation of tTF-NGR to improve the antitumor profile of the molecule. PEGylation resulted in an approximately 2-log step decreased procoagulatory activity of the molecule. Pharmacokinetic studies in mice showed a more than l-log step higher mean area under the curve. Comparison of the LD10 values for both compounds and their lowest effective antitumor dose against human tumor xenografts showed an improved therapeutic range (active/toxic dose in mg/kg body weight) of 1/5 mg/kg for tTF-NGR and 3/%26gt;160 mg/kg for TMS(PEG)(12), tTF-NGR. Results demonstrate that PEGylation can significantly improve the therapeutic range of tTF-NGR

• 出版日期2013-3-28