Induction of chemokine receptor CXCR4 expression by transforming growth factor-beta 1 in human basal cell carcinoma cells
Resource
J. Dermatol. Sci., 72(2), 123-133
Journal
J. Dermatol. Sci.
Journal Volume
72
Journal Issue
2
Pages
123-133
Date Issued
2013
Date
2013
Author(s)
Chu, Chia-Yu
Sheen, Yi-Shuan
Cha, Shih-Ting
Hu, Yeh-Fang
Tan, Ching-Ting
Chiu, Hsien-Ching
Chang, Cheng-Chi
Chen, Min-Wei
Kuo, Min-Liang
Jee, Shiou-Hwa
Abstract
Background: Higher CXCR4 expression enhances basal cell carcinoma (BCC) invasion and angiogenesis. The underlying mechanism of increased CXCR4 expression in invasive BCC is still not well understood. Objective: To investigate the mechanisms involved in the regulation of CXCR4 expression in invasive BCC.
Methods: We used qRT-PCR, RT-PCR, Western blot, and flow cytometric analyses to examine different CXCR4 levels among the clinical samples, co-cultured BCC cells and BCC cells treated with recombinant transforming growth factor-beta 1 (TGF-beta 1) and connective tissue growth factor (CTGF). Immunohistochemical studies were used to demonstrate the correlation between TGF-beta 1 and CXCR4 expressions. The signal transduction pathway and transcriptional regulation were confirmed by treatments with chemical inhibitors, neutralizing antibodies, or short interfering RNAs, as well as luciferase reporter activity.
Results: Invasive BCC has higher TGF-beta 1 and CTGF levels compared to non-invasive BCC. Non-contact dermal fibroblasts co-culture with human BCC cells also increases the expression of CXCR4 in BCC cells. Treatment with recombinant human TGF-beta 1, but not CTGF, enhanced the CXCR4 levels in time- and dose-dependent manners. The protein level and surface expression of CXCR4 in human BCC cells was increased by TGF-beta 1 treatment. TGF-beta 1 was intensely expressed in the surrounding fibroblasts of invasive BCC and was positively correlated with the CXCR4 expression of BCC cells. The transcriptional regulation of CXCR4 by TGF-beta 1 is mediated by its binding to the TGF-beta receptor II and phosphorylation of the extracellular signal-related kinase 1/2 (ERK1/2)-ETS-1 pathway.
Conclusion: TGF-beta 1 induces upregulation of CXCR4 in human BCC cells by phosphorylation of ERK1/2-ETS-1 pathway. (C) 2013 Japanese Society for Investigative Dermatology. Published by Elsevier Ireland Ltd. All rights reserved.
Methods: We used qRT-PCR, RT-PCR, Western blot, and flow cytometric analyses to examine different CXCR4 levels among the clinical samples, co-cultured BCC cells and BCC cells treated with recombinant transforming growth factor-beta 1 (TGF-beta 1) and connective tissue growth factor (CTGF). Immunohistochemical studies were used to demonstrate the correlation between TGF-beta 1 and CXCR4 expressions. The signal transduction pathway and transcriptional regulation were confirmed by treatments with chemical inhibitors, neutralizing antibodies, or short interfering RNAs, as well as luciferase reporter activity.
Results: Invasive BCC has higher TGF-beta 1 and CTGF levels compared to non-invasive BCC. Non-contact dermal fibroblasts co-culture with human BCC cells also increases the expression of CXCR4 in BCC cells. Treatment with recombinant human TGF-beta 1, but not CTGF, enhanced the CXCR4 levels in time- and dose-dependent manners. The protein level and surface expression of CXCR4 in human BCC cells was increased by TGF-beta 1 treatment. TGF-beta 1 was intensely expressed in the surrounding fibroblasts of invasive BCC and was positively correlated with the CXCR4 expression of BCC cells. The transcriptional regulation of CXCR4 by TGF-beta 1 is mediated by its binding to the TGF-beta receptor II and phosphorylation of the extracellular signal-related kinase 1/2 (ERK1/2)-ETS-1 pathway.
Conclusion: TGF-beta 1 induces upregulation of CXCR4 in human BCC cells by phosphorylation of ERK1/2-ETS-1 pathway. (C) 2013 Japanese Society for Investigative Dermatology. Published by Elsevier Ireland Ltd. All rights reserved.
Subjects
Basal cell carcinoma
Chemokine
Invasion
Transforming growth factor
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