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Expression and activation of α v β 3 integrins by SDF‐1/CXC12 increases the aggressiveness of prostate cancer cells
Author(s) -
Sun YanXi,
Fang Ming,
Wang Jianhua,
Cooper Carlton R.,
Pienta Kenneth J.,
Taichman Russell S.
Publication year - 2006
Publication title -
the prostate
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.295
H-Index - 123
eISSN - 1097-0045
pISSN - 0270-4137
DOI - 10.1002/pros.20500
Subject(s) - stromal cell , prostate cancer , cancer research , metastasis , receptor , prostate , cxcr4 , integrin , stromal cell derived factor 1 , biology , cancer cell , cancer , medicine , chemokine
BACKGROUND Stromal cell‐derived factor‐1 (SDF‐1 or CXCL12) and CXCR4 are key elements in the metastasis of prostate cancer cells to bone—but the mechanisms as to how it localizes to the marrow remains unclear. METHODS Prostate cancer cell lines were stimulated with SDF‐1 and evaluated for alterations in the expression of adhesion molecules using microarrays, FACs, and Western blotting to identify α v β 3 receptors. Cell–cell adhesion and invasion assays were used to verify that activation of the receptor is responsive to SDF‐1. RESULTS We demonstrate that SDF‐1 transiently regulates the number and affinity of α v β 3 receptors by prostate cancer cells to enhance their metastatic behavior by increasing adhesiveness and invasiveness. SDF‐1 transiently increased the expression of β 3 receptor subunit and increased its phosphorylation in metastatic but not nonmetastatic cells. CONCLUSIONS The transition from a locally invasive phenotype to a metastatic phenotype may be primed by the elevated expression of α v β 3 receptors. Activation and increased expression of α v β 3 within SDF‐1‐rich organs may participate in metastatic localization. Prostate 67:61–73, 2007. © 2006 Wiley‐Liss, Inc.