Tumor Vascular Targeting Using a Tumor-Tissue Endothelium-Specific Monoclonal Antibody as an Effective Strategy for Cancer Chemotherapy

In this study, we attempted to develop tumor vascular targeting with a tumor tissue endothelium-specific monoclonal antibody. TES-23, which strongly and selectively recognizes tumor tissue endothelial cells, was chemically conjugated with Neocarzinostatin (NCS), and the anti-tumor effect was examine...

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Veröffentlicht in:Biochemical and biophysical research communications 1999-07, Vol.260 (2), p.346-350
Hauptverfasser: Makimoto, Hiroo, Koizumi, Kei-ichi, Tsunoda, Shin-ichi, Wakai, Yukiko, Matsui, Junji, Tsutsumi, Yasuo, Nakagawa, Shinsaku, Ohizumi, Iwao, Taniguchi, Kenji, Saito, Hiroyuki, Utoguchi, Naoki, Ohsugi, Yoshiyuki, Mayumi, Tadanori
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Sprache:eng
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Zusammenfassung:In this study, we attempted to develop tumor vascular targeting with a tumor tissue endothelium-specific monoclonal antibody. TES-23, which strongly and selectively recognizes tumor tissue endothelial cells, was chemically conjugated with Neocarzinostatin (NCS), and the anti-tumor effect was examined. The immunoconjugate, TES-23-NCS, showed, through the use of tumor hemorrhagic necrosis, a marked anti-tumor effect on KMT-17 tumors in rats at a dosage of 17 μg/kg (NCS equivalent) without any side effects, probably due to specific tumor vascular injury. By contrast, TES-23 alone (107 μg/kg), NCS alone (17 μg/kg), and Mopc-NCS (Mopc, 107 μg/kg; NCS, 17 μg/kg), the immunoconjugate of control antibody, did not have any anti-tumor activities. By tissue distribution analysis, TES-23 and TES-23-NCS showed high accumulation in KMT-17 tumors 1 h after intravenous administration. Moreover TES-23 also accumulated in Sarcoma-180 tumors in mice 1 h after intravenous administration. These results suggest that TES-23 may be a candidate for a potential tumor vascular targeting agent that is applicable to a wide variety of tumor types.
ISSN:0006-291X
1090-2104
DOI:10.1006/bbrc.1999.0647