Dissemination of hepatocellular carcinoma is mediated via chemokine receptor CXCR4

被引:145
作者
Schimanski, C. C.
Bahre, R.
Gockel, I.
Mueller, A.
Frerichs, K.
Hoerner, V.
Teufel, A.
Simiantonaki, N.
Biesterfeld, S.
Wehler, T.
Schuler, M.
Achenbach, T.
Junginger, T.
Galle, P. R.
Moehler, M.
机构
[1] Univ Mainz, Dept Internal Med 1, D-55101 Mainz, Germany
[2] Univ Mainz, Dept Surg, D-55101 Mainz, Germany
[3] Univ Mainz, Dept Pathol, D-55101 Mainz, Germany
[4] Univ Mainz, Dept Internal Med, D-55101 Mainz, Germany
[5] Univ Mainz, Dept Radiol, D-55101 Mainz, Germany
关键词
CXCR4; chemokine; liver; hepatocellular; metastasis;
D O I
10.1038/sj.bjc.6603251
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In different tumour entities, expression of the chemokine receptor 4 ( CXCR4) has been linked to tumour dissemination and poor prognosis. Therefore, we evaluated, if the expression of CXCR4 exerts similar effects in human hepatocellular carcinoma ( HCC). Expression analysis and functional assays were performed in vitro to elucidate the impact of CXCL12 on human hepatoma cells lines. In addition, expression of CXCR4 was evaluated in 39 patients with HCC semiquantitatively and correlated with both, tumour and patients characteristics. Human HCC and hepatoma cell lines displayed variable intensities of CXCR4 expression. Loss of p53 function did not impact on CXCR4 expression. Exposure to CXCL12 mediated a perinuclear translocation of CXCR4 in Huh7/ Hep3B cells and increased the invasive potential of Huh7 cells. In HCC patients, CXCR4 expression significantly correlated with progressed local tumours ( T- status; P 0.006), lymphatic metastasis ( N- status; P 0.005) and distant dissemination ( M- status; P = 0.009), as well as with a decreased 3- year- survival rate (P = 0.01). In summary, strong expression of CXCR4 is significantly associated with progressed hepatocellular cancer.
引用
收藏
页码:210 / 217
页数:8
相关论文
共 32 条
[1]   Chemokines: key players in cancer [J].
Arya, M ;
Patel, HRH ;
Williamson, M .
CURRENT MEDICAL RESEARCH AND OPINION, 2003, 19 (06) :557-564
[2]   Inflammation and cancer: back to Virchow? [J].
Balkwill, F ;
Mantovani, A .
LANCET, 2001, 357 (9255) :539-545
[3]   Epidemiology of primary liver cancer [J].
Bosch, FX ;
Ribes, J ;
Borràs, J .
SEMINARS IN LIVER DISEASE, 1999, 19 (03) :271-285
[4]   Functional expression of CXCR4 (CD184) on small-cell lung cancer cells mediates migration, integrin activation, and adhesion to stromal cells [J].
Burger, M ;
Glodek, A ;
Hartmann, T ;
Schmitt-Gräff, A ;
Silberstein, LE ;
Fujii, N ;
Kipps, TJ ;
Burger, JA .
ONCOGENE, 2003, 22 (50) :8093-8101
[5]  
Cardones AR, 2003, CANCER RES, V63, P6751
[6]  
Chen YC, 2003, CANCER RES, V63, P4801
[7]   Genetic mechanisms of hepatocarcinogenesis [J].
Feitelson, MA ;
Sun, B ;
Tufan, NLS ;
Liu, J ;
Pan, JB ;
Lian, ZR .
ONCOGENE, 2002, 21 (16) :2593-2604
[8]   Differential expression of chemokines and chemokine receptors shapes the inflammatory response in rejecting human liver transplants [J].
Goddard, S ;
Williams, A ;
Morland, C ;
Qin, SX ;
Gladue, R ;
Hubscher, SG ;
Adams, DH .
TRANSPLANTATION, 2001, 72 (12) :1957-1967
[9]  
Hatch Heather M., 2002, Cloning and Stem Cells, V4, P339, DOI 10.1089/153623002321025014
[10]   NF-κB promotes breast cancer cell migration and metastasis by inducing the expression of the chemokine receptor CXCR4 [J].
Helbig, G ;
Christopherson, KW ;
Bhat-Nakshatri, P ;
Kumar, S ;
Kishimoto, H ;
Miller, KD ;
Broxmeyer, HE ;
Nakshatri, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (24) :21631-21638