4.8 Article

CX3CR1-fractalkine expression regulates cellular mechanisms involved in adhesion, migration, and survival of human prostate cancer cells

Journal

CANCER RESEARCH
Volume 64, Issue 14, Pages 4693-4698

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/0008-5472.CAN-03-3437

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Funding

  1. NCI NIH HHS [CA 076639-07] Funding Source: Medline
  2. NIDA NIH HHS [DA 15014-01, R01 DA015014-03, R01 DA019808-01, R01 DA015014-01, R01 DA015014-02] Funding Source: Medline
  3. NIGMS NIH HHS [GM 067892] Funding Source: Medline

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Chemokines and their receptors might be involved in the selection of specific organs by metastatic cancer cells. For instance, the CXCR4-SDF-1alpha pair regulates adhesion and migration of breast as well as prostate cancer cells to metastatic sites. In this study, we present the first evidence for the expression of CX3CR1-the specific receptor for the chemokine fractalkine-by human prostate cancer cells, whereas human bone marrow endothelial cells and differentiated osteoblasts; express fractalkine. The adhesion of prostate cancer cells to human bone marrow endothelial cells in flow conditions is significantly reduced by a neutralizing antibody against fractalkine, and they migrate toward a medium conditioned by osteoblasts, which secrete the soluble form of the chemokine. Finally, fractalkine activates the PI3K/Akt survival pathway in human prostate cancer cells.

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