CXCR6-CXCL16 axis promotes prostate cancer by mediating cytoskeleton rearrangement via Ezrin activation and αvβ3 integrin clustering

• Published in: Oncotarget Vol. 7; no. 6; pp. 7343 - 7353
• Main Authors: Singh, Rajesh, Kapur, Neeraj, Mir, Hina, Singh, Nalinaksha, Lillard, Jr, James W, Singh, Shailesh
• Format: Journal Article
• Language: English
• Published: United States Impact Journals LLC 09-02-2016
• Subjects: Apoptosis; Blotting, Western; Cell Adhesion; Cell Movement; Cell Proliferation; Chemokine CXCL16; Chemokines, CXC - genetics; Chemokines, CXC - metabolism; Cytoskeletal Proteins - genetics; Cytoskeletal Proteins - metabolism; Cytoskeleton - genetics; Cytoskeleton - metabolism; Cytoskeleton - pathology; Flow Cytometry; Humans; Image Processing, Computer-Assisted; Immunoenzyme Techniques; Integrin alphaVbeta3 - genetics; Integrin alphaVbeta3 - metabolism; Male; Prostatic Neoplasms - genetics; Prostatic Neoplasms - metabolism; Prostatic Neoplasms - pathology; Real-Time Polymerase Chain Reaction; Receptors, Chemokine - genetics; Receptors, Chemokine - metabolism; Receptors, CXCR6; Receptors, Scavenger - genetics; Receptors, Scavenger - metabolism; Receptors, Virus - genetics; Receptors, Virus - metabolism; Research Paper; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger - genetics; Tumor Cells, Cultured; prostate cancer; CXCR6; αvβ3 integrin; Ezrin; CXCL16
• ISSN: 1949-2553; 1949-2553
• DOI: 10.18632/oncotarget.6944

Cytoskeletal rearrangement is required for migration and invasion, which are the key steps of cancer metastasis. Ezrin and integrin co-ordinate these processes by regulating cellular adhesion and cytoskeletal polymerization-depolymerization. It is also well established that chemokine-chemokine receptor axis plays a crucial role in regulating cancer cell migration and invasion. In this study, we show involvement of CXC chemokine receptor 6 (CXCR6) and its only natural ligand CXCL16 in pathobiology of prostate cancer (PCa). CXCR6 is highly expressed in PCa tissues and cell lines (LNCaP and PC3), relative to normal tissue and cells. CXCR6 expression in PCa tissues correlated with higher Gleason score. Similarly, aggressive PCa cells (PC3) show high CXCR6 compared to less aggressive LNCaP. Besides, PC3 cells show higher MMPs expression compared to LNCaP cells following CXCL16 stimulation. Intriguingly, CXCR6-CXCL16 interaction in PCa cells promotes Ezrin activation, αvβ3 integrin clustering and capping at the leading edge in FAK/PI3K/PKC dependent manner, thereby modifying cellular adhesion as well as motility. Together these results demonstrate that CXCL16 stimulation changes cytoskeletal dynamics resulting in enhanced migration, invasion and adhesion to endothelial cells, ultimately enabling PCa cells to achieve their metastatic goal.