Full-length soluble CD147 promotes MMP-2 expression and is a potential serological marker in detection of hepatocellular carcinoma

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Abstract

Background: As a surface glycoprotein, CD147 is capable of stimulating the production of matrix metalloproteinases (MMPs) from neighboring fibroblasts. The aim of the present study is to explore the role of soluble CD147 on MMPs secretion from hepatocellular carcinoma (HCC) cells, and to investigate the diagnostic value of serum soluble CD147 in the HCC detection.Methods: We identified the form of soluble CD147 in cell culture supernate of HCC cells and serum of patients with HCC, and explored the role of soluble CD147 on MMPs secretion. Serum CD147 levels were detected by the enzyme-linked immunosorbent assay, and the value of soluble CD147 as a marker in HCC detection was analyzed.Results: Full length soluble CD147 was presented in the culture medium of HCC cells and serum of patients with HCC. The extracellular domain of soluble CD147 promoted the expression of CD147 and MMP-2 from HCC cells. Knockdown of CD147 markedly diminished the up-regulation of CD147 and MMP-2 which induced by soluble CD147. Soluble CD147 activated ERK, FAK, and PI3K/Akt pathways, leading to the up-regulation of MMP-2. The level of soluble CD147 in serum of patients with HCC was significantly elevated compared with healthy individuals (P < 0.001). Soluble CD147 levels were found to be associated with HCC tumor size (P = 0.007) and Child-Pugh grade (P = 0.007). Moreover, soluble CD147 showed a better performance in distinguishing HCC compared with alpha-fetoprotein.Conclusions: The extracellular domain of soluble CD147 enhances the secretion of MMP-2 from HCC cells, requiring the cooperation of membrane CD147 and activation of ERK, FAK, and PI3K/Akt signaling. The measurement of soluble CD147 may offer a useful approach in diagnosis of HCC.

Figures

  • Table 1 Sequences of real-time PCR primers
  • Table 2 Clinical and demographic characteristics of patients with HCC
  • Figure 1 MMPs expression in HCC cells under the stimulation of soluble CD147. Eukaryotically expressed extracellular CD147 (E-CD147ECD), serum-free conditioned medium, and SMMC-7721 cell lysates were subjected to western blotting. HAb18 reacting against extracellular CD147 (A) and C-19 reacting against intracellular CD147 (B) were used respectively. (C) Real-time PCR was performed to test mRNA levels of MMP-1, −2, −3, −9, and MMP-13 in SMMC-7721 cells in the absence or presence of 10 μg/ml E-CD147ECD for 6 h. (D) Soluble CD147 increased the expression of MMP-2 in a concentration-dependent manner. SMMC-7721 cells were treated with different concentrations of E-CD147ECD for 6 h and MMP-2 mRNA level was analyzed using real-time PCR. (E) SMMC-7721 cells were treated with different concentrations of E-CD147ECD and MMPs levels were analyzed using gelatin zymography. (F) SMMC-7721 cells were treated with prokaryotically expressed extracellular CD147 (P-CD147ECD) or E-CD147ECD for 6 h and MMP-2 mRNA level was analyzed using real-time PCR. GAPDH was used as a normalization control. *P < 0.05. (G) Real-time PCR showed mRNA level of MMP-2 in SMMC-7721 cells treated with P-CD147ECD or prokaryotically expressed intracellular CD147 (P-CD147ICD) for 6 h. GAPDH was used as a normalization control in all real-time PCR analysis. *P < 0.05, **P < 0.01.
  • Figure 2 (See legend on next page.)
  • Figure 3 Involvement of ERK, FAK, and PI3K/Akt pathways in upregul cultured for 30 min (A) and 12 h (B) with 10 μg/ml of E-CD147ECD. CD147 an determinations of CD147 or MMP-2/α-tubulin ratio. (C) SMMC-7721 cells w pre-treatment with ERK inhibitor (U0126), FAK inhibitor (FAK inhibitor 14), expression levels of phospho-ERK1/2, ERK1/2, phospho-FAK, FAK, phospho blotting. Quantitative analysis of phosphorylated fraction relative to the total f to 1. *P < 0.05, **P < 0.01, ***P < 0.001.
  • Figure 4 (See legend on next page.)
  • Table 4 Relationship between serum MMP-2 and variable clinicopathologic features
  • Figure 5 ROC curves used to predict performance of soluble CD147 for distinguishing HCC from healthy controls. (A) ROC curve evaluating those with HCC (n = 62) and healthy controls (n = 25). (B) ROC curve evaluating those with AFP-negative HCC (n = 33) and healthy controls (n = 25). (C) ROC curve evaluating those with early stage HCC (n = 31) and healthy controls (n = 25). (D) ROC curve evaluating those with very early stage HCC (n = 12) and healthy controls (n = 25).

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Wu, J., Hao, Z. W., Zhao, Y. X., Yang, X. M., Tang, H., Zhang, X., … Bian, H. (2014). Full-length soluble CD147 promotes MMP-2 expression and is a potential serological marker in detection of hepatocellular carcinoma. Journal of Translational Medicine, 12(1). https://doi.org/10.1186/1479-5876-12-190

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