Expression of CXC chemokine receptors 1-5 and their ligands in human glioma tissues: Role of CXCR4 and SDF1 in glioma cell proliferation and migration

被引:127
作者
Bajetto, Adriana
Barbieri, Federica
Dorcaratto, Alessandra
Barbero, Simone
Daga, Antonio
Porcile, Carola
Ravetti, Jean Louis
Zona, Gianluigi
Spaziante, Renato
Corte, Giorgio
Schettini, Gennaro
Florio, Tullio
机构
[1] Univ Genoa, Dept Oncol Biol & Genet, I-16132 Genoa, Italy
[2] Dept Surg Anaesthesiol & Transplants, Neurosurg Sect, Genoa, Italy
[3] Osped San Martino Genova, Sect Pathol, Genoa, Italy
[4] Univ Genoa, Dept Neurosci Ophthalmol & Genet, Neurosurg Sect, Genoa, Italy
[5] Natl Inst Canc Res, Expt Oncol Lab, Genoa, Italy
关键词
chemokine; CXCR4; SDF1; glioma; cell migration; cell proliferation;
D O I
10.1016/j.neuint.2006.03.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chemokines have been involved in cellular processes associated to malignant transformation such as proliferation, migration and angiogenesis. The expression of five CXC chemokine receptors and their main ligands was analysed by RT-PCR in 31 human astrocytic neoplasms. The mRNAs for all the receptors analysed were identified in a high percentage of tumours, while their ligands showed lower expression. CXCR4 and SDF1 were the most frequently mRNA identified (29/31 and 13/31 of the gliomas studied, respectively). Thus, we further analysed the cell localization of CXCR4 and SDF1 in immunohistochemistry experiments. We show a marked co-localization of CXCR4 and SDF1 in tumour cells, mainly evident in psudolpalisade and microcystic degeneration areas and in the vascular endothelium. In addition, hSDF1 alpha induced a significant increase of DNA synthesis in primary human glioblastoma cell cultures and chemotaxis in a glioblastoma cell line. These results provide evidence of the expression of multiple CXC chemokines and their receptors in brain tumours and that in particular CXCR4 and SDF1 sustain proliferation and migration of glioma cells to promote malignant progression. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:423 / 432
页数:10
相关论文
共 49 条
  • [41] Sehgal A, 1998, J SURG ONCOL, V69, P99, DOI 10.1002/(SICI)1096-9098(199810)69:2<99::AID-JSO10>3.0.CO
  • [42] 2-M
  • [43] Chemokine receptor CXCR4 downregulated by von Hippel-Lindau tumour suppressor pVHL
    Staller, P
    Sulitkova, J
    Liszlwan, J
    Moch, H
    Oakeley, EJ
    Krek, W
    [J]. NATURE, 2003, 425 (6955) : 307 - 311
  • [44] Expression of CXCR4 and CXCL12 (SDF-1) in human prostate cancers (PCa) in vivo
    Sun, YX
    Wang, JC
    Shelburne, CE
    Lopatin, DE
    Chinnaiyan, AM
    Rubin, MA
    Pienta, KJ
    Taichman, RS
    [J]. JOURNAL OF CELLULAR BIOCHEMISTRY, 2003, 89 (03) : 462 - 473
  • [45] Stromal cell-derived factor-1α and CXCR4 expression in hermangioblastoma and clear cell-renal cell carcinoma:: von Hippe-Lindau loss-of-function induces expression of a ligand and its receptor
    Zagzag, D
    Krishnamachary, B
    Yee, H
    Okuyama, H
    Chiriboga, L
    Ali, MA
    Melamed, J
    Semenza, GL
    [J]. CANCER RESEARCH, 2005, 65 (14) : 6178 - 6188
  • [46] The chemokine GRO-α (CXCL1) confers increased tumorigenicity to glioma cells
    Zhou, Y
    Zhang, J
    Liu, Q
    Bell, R
    Muruve, DA
    Forsyth, P
    Arcellana-Panlilio, M
    Robbins, S
    Yong, VW
    [J]. CARCINOGENESIS, 2005, 26 (12) : 2058 - 2068
  • [47] CXCRA is a major chemokine receptor on glioma cells and mediates their survival
    Zhou, Y
    Larsen, PH
    Hao, CH
    Yong, VW
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (51) : 49481 - 49487
  • [48] Zlotnik A, 2004, SEMIN CANCER BIOL, V14, P181, DOI 10.1016/j.semcancer.2003.10.004
  • [49] Function of the chemokine receptor CXCR4 in haematopoiesis and in cerebellar development
    Zou, YR
    Kottmann, AH
    Kuroda, M
    Taniuchi, I
    Littman, DR
    [J]. NATURE, 1998, 393 (6685) : 595 - 599