4.6 Article

AsialoGM1 and integrin α2β1 mediate prostate cancer progression

Journal

INTERNATIONAL JOURNAL OF ONCOLOGY
Volume 35, Issue 4, Pages 693-699

Publisher

SPANDIDOS PUBL LTD
DOI: 10.3892/ijo_00000381

Keywords

adhesion; migration; invasion; extracellular matrix; glycosphingolipid; prostate cancer

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Funding

  1. US National Institutes of Health [RR-16480]
  2. New Mexico Tech
  3. New Mexico Department of Veteran Services

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The most lethal aspect of cancer is the metastatic spread of primary tumors to distant sites. Any mechanism revealed is a target for therapy. In our previous studies, we reported that the invasive activity of the bone metastatic C4-2B prostate cancer cells could be ascribed to the reorganization of the alpha 2 beta 1 integrin receptor and the alpha 2 subunit-mediated association and activation of downstream signaling towards the activation of MMPs. In the present study, we demonstrate that expression of asialoGM1 in C4-2B cells correlates with cancer progression by influencing adhesion, migration and invasion, via reorganization of asialoGM1 and colocalization with integrin alpha 2 beta 1. These observations reveal an uncharacterized complex of asialoGM1 with the integrin alpha 2 beta 1 receptor promoting cancer metastatic potential through the previously identified integrin-mediated signaling pathway. The present findings promote further understanding of mechanisms by which glycosphingolipids modulate malignant properties and the results obtained here propose novel directions for future study.

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