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Inhibition of Tumor Growth and Metastasis by Korean Mistletoe Lectin is Associated with Apoptosis and Antiangiogenesis

To cite this article:
Won-Bong Park, Su-Yun Lyu, Jong-Huyn Kim, Sang-Ho Choi, Ho-Kwon Chung, Sang-Hun Ahn, Sung-Youl Hong, Taek-Joon Yoon, and Myeong-Jun Choi. Cancer Biotherapy & Radiopharmaceuticals. October 2001, 16(5): 439-447. doi:10.1089/108497801753354348.

Published in Volume: 16 Issue 5: July 5, 2004

Author information

Won-Bong Park
College of Natural Science, Seoul Women's University, Seoul 139-774, Korea
Su-Yun Lyu
College of Natural Science, Seoul Women's University, Seoul 139-774, Korea
Jong-Huyn Kim
College of Natural Science, Seoul Women's University, Seoul 139-774, Korea
Sang-Ho Choi
College of Natural Science, Seoul Women's University, Seoul 139-774, Korea
Ho-Kwon Chung
Charmzone Biomaterial Institute, 301 Hangang B/D, 184-11, Kwangjang-dong, Kwangjin-gu, Seoul 143-210, Korea
Sang-Hun Ahn
Department of Genetic Engineering, Sungkyunkwan University, Suwon 440-746, Korea
Sung-Youl Hong
Department of Genetic Engineering, Sungkyunkwan University, Suwon 440-746, Korea
Taek-Joon Yoon
Department of Oncology, Graduate School of East-West Medicine, Kyunghee University, Seouchunri, Kihung-eup, Yongin-si, Kyungki-do. 449-701, Korea
Myeong-Jun Choi
Drug Delivery Research Laboratory, Mogam Biotechnology Research Institute, 341 Pojung-ri, Koosung-Myun, Yongin City, Kyonggi-Do 449-910, Korea

ABSTRACT

The mistletoe lectins are major active components in the extract of European mistletoes that have been widely used in adjuvant chemotherapy of cancer. This study was performed to investigate the mechanism of anticancer and antimetastatic activity of the purified Korean mistletoe lectin (Viscum album L. coloratum agglutinin, VCA). C57BL6 mice inoculated with B16-BL6 melanoma cells and treated with VCA were assessed for survival and metastasis. The induction of apoptosis of B16-BL6 cells by VCA was investigated by morphological changes, DNA fragmentation characteristics, and cell cycle analysis. The antiangiogenic activity of VCA was also measured by the CAM (chorioallantoic membrane) assay. Length of survival of mice was increased and lung metastasis was inhibited by VCA. Treatment of cells with VCA resulted in growth suppression, nuclear morphological changes, DNA fragmentation, and an increased fraction of cells in sub-G1 consistent with apoptosis. Antiangiogenesis of VCA was assessed by CAM assay, where vessel growth induced by fat emulsion was decreased. These results suggest that VCA inhibits tumor growth and metastasis by increasing apoptosis and inhibiting angiogenesis.

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