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Clinical and biological significance of CXCR5 expressed by prostate cancer specimens and cell lines
International Journal of Cancer, 07/29/09
Singh S et al. - In a study to we show whether primary prostate cancer (PCa) tissues and cell lines (LNCaP and PC3) express CXCR5, a specific chemokine receptor for CXCL13, it was concluded that these data demonstrate the clinical and biological relevance of the CXCL13-CXCR5 pathway and its role in PCa cell invasion and migration.
Methods- Chemokines and chemokine receptors have been shown to be involved in metastatic process of PCa.
- It was tested whether primary PCa tissues and cell lines (LNCaP and PC3) express CXCR5, a specific chemokine receptor for CXCL13.
- Expression of CXCR5 was significantly higher in PCa cases vs normal match (NM) tissues.
- CXCR5 intensity correlated (R2 = 0.97) with Gleason score.
- While prostate tumor tissues with Gleason scores ≥7, displayed predominantly nuclear CXCR5 expression patterns, PCa specimens with Gleason scores ≤6 showed predominantly membrane and cytoplasmic expression patterns that were comparable to benign prostatic hyperplasia (BPH).
- Similar to tissue expression, PCa cell lines expressed significantly more CXCR5 than normal prostatic epithelial cells (PrECs), and CXCR5 expression was distributed among intracellular and extracellular compartments.
- Functional in vitro assays showed higher migratory and invasive potentials toward CXCL13, an effect that was mediated by CXCR5.
- In both PCa cell lines, CXCL13 treatment increased expression of collagenase-1 or matrix metalloproteinase-1 (MMP-1), collagenase-3 (MMP-13), stromelysin-1 (MMP-3), stromelysin-2 (MMP-10) and stromelysin-3 (MMP-11).
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