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Glycosphingolipid GM2 Induces Invasiveness in Irradiation-tolerant Lung Cancer Cells.
Ishihara, Seiichiro; Aoki, Kei; Mizutani, Takeomi; Amano, Maho; Nishimura, Shin-Ichiro; Haga, Hisashi.
Affiliation
  • Ishihara S; Faculty of Advanced Life Science, Hokkaido University.
  • Aoki K; Faculty of Advanced Life Science, Hokkaido University.
  • Mizutani T; Department of Life Science and Technology, Faculty of Engineering, Hokkai-Gakuen University.
  • Amano M; Faculty of Advanced Life Science, Hokkaido University.
  • Nishimura SI; Faculty of Advanced Life Science, Hokkaido University.
  • Haga H; Faculty of Advanced Life Science, Hokkaido University.
Cell Struct Funct ; 43(2): 177-185, 2018.
Article in En | MEDLINE | ID: mdl-30404974
ABSTRACT
Glycans, including glycosphingolipids, are broadly expressed in plasma membranes and play important roles in cell-cell interactions. Recently, it has been revealed that glycans participate in the regulation of malignant phenotypes of cancer cells, e.g. growth and invasion. However, their roles in irradiation-tolerant cancer cells have not yet been elucidated. In this study, we show that specific glycosphingolipids are highly expressed in invasive, irradiation-tolerant lung cancer cells. Particularly, the glycosphingolipid GM2 contributes to the development of an invasive phenotype in these lung cancer cells. Our results suggest that glycosphingolipids, including GM2, are implicated in the regulation of invasiveness in irradiation-tolerant lung cancer cells and may therefore serve as potential therapeutic targets for lung cancers following radiotherapy.Key words glycosphingolipids, GM2, invasion, lung cancer cells, radiotherapy.
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Full text: 1 Database: MEDLINE Main subject: Glycosphingolipids / G(M2) Activator Protein / Lung Neoplasms Type of study: Prognostic_studies Limits: Humans Language: En Journal: Cell Struct Funct Year: 2018 Type: Article

Full text: 1 Database: MEDLINE Main subject: Glycosphingolipids / G(M2) Activator Protein / Lung Neoplasms Type of study: Prognostic_studies Limits: Humans Language: En Journal: Cell Struct Funct Year: 2018 Type: Article