Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1940537 | Biochemical and Biophysical Research Communications | 2006 | 7 Pages |
Abstract
N-Glycan structures on the surface of cancer cells have diverse structures and play significant roles in metastatic process. However, little is known about their roles in organ-selective metastasis. Our study revealed that an α1,6-fucosylated biantennary N-glycan structure designated A2G2F is characteristic of lungs, with far more abundant expression in normal human and murine lungs than in other organs. In this study, we further examined the role of A2G2F in pulmonary metastasis. We stained metastatic cancers by α1,6-fucose-specific Lens culinaris agglutinin lectin and revealed that pulmonary metastatic nodules more abundantly expressed α1,6-fucosylated N-glycans than hepatic metastatic nodules from common primary cancers. The most specific α1,6-fucosylated N-glycan structure in pulmonary metastatic cancer was identified to be A2G2F. Using a B16 melanoma cell metastasis model, we showed that A2G2F-rich B16 cells formed more pulmonary metastatic nodules than A2G2F-poor cells. Our results suggest that A2G2F plays a critical role in pulmonary metastasis.
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Authors
Keiichiro Sakuma, Ichiro Fujimoto, Seiji Hitoshi, Fumihiro Tanaka, Takeshi Ikeda, Kazuhiro Tanabe, Shinya Toyokuni, Hiromi Wada, Tadashi Mio, Michiaki Mishima, Kazuhiro Ikenaka,