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[Cancer Research 64, 6252-6258, September 1, 2004]
© 2004 American Association for Cancer Research


Regular Articles

Growth Inhibition of Human Prostate Cancer Cells in Human Adult Bone Implanted into Nonobese Diabetic/Severe Combined Immunodeficient Mice by a Ligand-Specific Antibody to Human Insulin-Like Growth Factors

Masato Goya1, Shin’ichi Miyamoto1, Kanji Nagai2, Yuji Ohki3, Kazuyasu Nakamura3, Kenya Shitara3, Hiroyuki Maeda1, Takafumi Sangai1, Keiji Kodama1, Yasushi Endoh1, Genichiro Ishii1, Takahiro Hasebe1, Hiroyuki Yonou4, Tadashi Hatano4, Yoshihide Ogawa4 and Atsushi Ochiai1

1 Pathology Division, National Cancer Center Research Institute East, Chiba; 2 Division of Thoracic Oncology, National Cancer Center Hospital East, Chiba; 3 Tokyo Research Laboratories, Kyowa Hakko Kogyo Co., Ltd., Machida, Tokyo; and 4 Department of Urology, University of the Ryukyus, Okinawa, Japan

Advanced prostate cancer frequently involves the bone that has the largest content of insulin-like growth factors (IGFs). However, the role of bone-derived IGFs in bone metastasis of prostate cancer has not been studied extensively because of the lack of a reliable animal model. Therefore, we investigated whether a novel antibody directed against human IGF-I and IGF-II (KM1468) could inhibit the development of new bone tumors and the progression of established bone tumors in nonobese diabetic/severe combined immunodeficient mice implanted with human adult bone. We first confirmed that KM1468 bound specifically to human IGF-I, human IGF-II, and mouse IGF-II but not to insulin. It also blocked autophosphorylation of the type I IGF receptor induced by the binding of IGFs in human-type I IGF receptor-overexpressing BALB/c 3T3 cells, and it inhibited the IGF-stimulated growth of MDA PCa 2b cells in vitro. Then mice were injected intraperitoneally with KM1468 once weekly for 4 weeks either immediately or 4 weeks after inoculation of MDA PCa 2b cells. KM1468 markedly and dose-dependently suppressed the development of new bone tumors and the progression of established tumor foci, as determined by histomorphometry, and it also decreased serum prostate-specific antigen levels, compared with the control. This is the first report of an IGF ligand-specific inhibitory antibody that suppresses the growth of human prostate cancer cells in human adult bone. These results indicate that the IGF signaling axis is a potential target for prevention and treatment of bone metastases arising from prostate cancer.




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