TY - JOUR
T1 - Tumor vascular targeting using a tumor-tissue endothelium-specific monoclonal antibody as an effective strategy for cancer chemotherapy
AU - Makimoto, Hiroo
AU - Koizumi, Kei Ichi
AU - Tsunoda, Shin Ichi
AU - Wakai, Yukiko
AU - Matsui, Junji
AU - Tsutsumi, Yasuo
AU - Nakagawa, Shinsaku
AU - Ohizumi, Iwao
AU - Taniguchi, Kenji
AU - Saito, Hiroyuki
AU - Utoguchi, Naoki
AU - Ohsugi, Yoshiyuki
AU - Mayumi, Tadanori
N1 - Funding Information:
This study was supported in part by Grants-in Aid for Scientific Research on Priority Areas (Cancer/Biotarget), for Scientific Research and for Encouragement of Young Scientists from the Ministry of Education, Science, Sports, and Culture of Japan, and in part by Health Sciences Research Grants for Research on Health Sciences focusing on Drug Innovation from Ministry of Health and Welfare.
PY - 1999/7/5
Y1 - 1999/7/5
N2 - 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 antitumor 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.
AB - 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 antitumor 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.
KW - Immunoconjugate
KW - Missile therapy
KW - Tumor vasculature
KW - Tumor-tissue endothelial cells
UR - http://www.scopus.com/inward/record.url?scp=0033526833&partnerID=8YFLogxK
U2 - 10.1006/bbrc.1999.0647
DO - 10.1006/bbrc.1999.0647
M3 - 学術論文
C2 - 10403773
AN - SCOPUS:0033526833
SN - 0006-291X
VL - 260
SP - 346
EP - 350
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 2
ER -