Crosstalk between chemokine receptor CXCR4 and cannabinoid receptor CB2 in modulating breast cancer growth and invasion

• Published in: PloS one Vol. 6; no. 9; p. e23901
• Main Authors: Nasser, Mohd W, Qamri, Zahida, Deol, Yadwinder S, Smith, Diane, Shilo, Konstantin, Zou, Xianghong, Ganju, Ramesh K
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 07.09.2011; Public Library of Science (PLoS)
• Subjects: Angiogenesis; Animal tissues; Animals; Biology; Blotting, Western; Brain; Breast cancer; Breast Neoplasms - metabolism; Cancer; Cannabinoid CB1 receptors; Cannabinoid CB2 receptors; Cell adhesion & migration; Cell culture; Cell cycle; Cell Line, Tumor; Cell Movement - drug effects; Chemokine CXCL12 - pharmacology; Chemokines; Chemotaxis; Confocal microscopy; Crosstalk; CXCL12 protein; CXCR4 protein; Cytoskeleton; Extracellular signal-regulated kinase; Female; Flow Cytometry; Humans; Immunoglobulins; Immunohistochemistry; In vivo methods and tests; Indoles - pharmacology; Inhibition; Kinases; Laboratories; Leukemia; Ligands; Liver cancer; Medical innovations; Medical prognosis; Medicine; Membranes; Metastases; Metastasis; Mice; Microscopy; Microscopy, Confocal; Molecular modelling; Pathology; Phosphorylation; Phosphorylation - drug effects; Proteins; Receptor, Cannabinoid, CB2 - agonists; Receptor, Cannabinoid, CB2 - metabolism; Receptors; Receptors, CXCR4 - metabolism; Signal transduction; Signaling; Tumors; Wound healing; Xenograft Model Antitumor Assays; United States > US; Ohio
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0023901

Cannabinoids bind to cannabinoid receptors CB(1) and CB(2) and have been reported to possess anti-tumorigenic activity in various cancers. However, the mechanisms through which cannabinoids modulate tumor growth are not well known. In this study, we report that a synthetic non-psychoactive cannabinoid that specifically binds to cannabinoid receptor CB(2) may modulate breast tumor growth and metastasis by inhibiting signaling of the chemokine receptor CXCR4 and its ligand CXCL12. This signaling pathway has been shown to play an important role in regulating breast cancer progression and metastasis. We observed high expression of both CB(2) and CXCR4 receptors in breast cancer patient tissues by immunohistochemical analysis. We further found that CB(2)-specific agonist JWH-015 inhibits the CXCL12-induced chemotaxis and wound healing of MCF7 overexpressing CXCR4 (MCF7/CXCR4), highly metastatic clone of MDA-MB-231 (SCP2) and NT 2.5 cells (derived from MMTV-neu) by using chemotactic and wound healing assays. Elucidation of the molecular mechanisms using various biochemical techniques and confocal microscopy revealed that JWH-015 treatment inhibited CXCL12-induced P44/P42 ERK activation, cytoskeletal focal adhesion and stress fiber formation, which play a critical role in breast cancer invasion and metastasis. In addition, we have shown that JWH-015 significantly inhibits orthotopic tumor growth in syngenic mice in vivo using NT 2.5 cells. Furthermore, our studies have revealed that JWH-015 significantly inhibits phosphorylation of CXCR4 and its downstream signaling in vivo in orthotopic and spontaneous breast cancer MMTV-PyMT mouse model systems. This study provides novel insights into the crosstalk between CB(2) and CXCR4/CXCL12-signaling pathways in the modulation of breast tumor growth and metastasis. Furthermore, these studies indicate that CB(2) receptors could be used for developing innovative therapeutic strategies against breast cancer.