The role of the CXCR4 cell surface chemokine receptor in glioma biology

被引:26
|
作者
Ehtesham, Moneeb [1 ]
Min, Elliot [1 ]
Issar, Neil M. [1 ]
Kasl, Rebecca A. [1 ]
Khan, Imad S. [1 ]
Thompson, Reid C. [1 ]
机构
[1] Vanderbilt Univ, Dept Neurol Surg, Med Ctr, Med Ctr N, Nashville, TN 37232 USA
关键词
CXCR4; CXCL12; Chemokine receptor; Glioma; Glioblastoma multiforme; Cancer; HYPOXIA-INDUCIBLE FACTOR-1; PROSTATE-CANCER METASTASIS; FACTOR-I; ANTAGONIST CTCE-9908; SMALL-MOLECULE; TUMOR-GROWTH; EXPRESSION; GLIOBLASTOMA; INHIBITION; MIGRATION;
D O I
10.1007/s11060-013-1108-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
CXCR4, a cell surface chemokine receptor, mediates cellular dissemination, invasion, and proliferation in a wide range of cancers including gliomas. It is over-expressed in glioma progenitor cells, and its protein ligand, CXCL12, has been shown to mediate a specific proliferative response in these cells thereby implicating a role for CXCR4 in glioma initiation and renewal. Given the failure of currently employed therapies to meaningfully impact prognosis in patients with high-grade gliomas, the CXCR4-CXCL12 axis represents a novel biologically relevant mechanism that could be specifically targeted for therapy. From this perspective, this review summarizes the biological effects of CXCR4 activity and its implications for glioma pathogenesis. Ultimately, the development of effective treatment approaches for malignant glioma must be based on a rational mechanistic understanding of tumor cell biology. As such, this article presents such a framework with regard to the CXCR4 pathway in glioma thereby supporting the further investigation of CXCR4 as a therapeutic target in patients with this disease.
引用
收藏
页码:153 / 162
页数:10
相关论文
共 50 条
  • [41] The good and bad faces of the CXCR4 chemokine receptor
    Teixido, Joaquin
    Martinez-Moreno, Monica
    Diaz-Martinez, Marta
    Sevilla-Movilla, Silvia
    INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2018, 95 : 121 - 131
  • [42] CXCR4 chemokine receptor antagonists: perspectives in SCLC
    Burger, Jan A.
    Stewart, David J.
    EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2009, 18 (04) : 481 - 490
  • [43] Expression of chemokine receptor CXCR4 enhances tumorigenesis of basal cell carcinoma
    Wu, M
    Chen, G
    Yu, H
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2004, 122 (03) : A18 - A18
  • [44] The chemokine receptor CXCR4 regulates cell-cycle proteins in neurons
    Muhammad Zafrullah Khan
    Renato Brandimarti
    Brian Joseph Musser
    Danielle Marie Resue
    Alessandro Fatatis
    Olimpia Meucci
    Journal of NeuroVirology, 2003, 9 : 300 - 314
  • [45] The chemokine receptor CXCR4 regulates cell-cycle proteins in neurons
    Khan, MZ
    Brandimarti, R
    Musser, BJ
    Resue, DM
    Fatatis, A
    Meucci, O
    JOURNAL OF NEUROVIROLOGY, 2003, 9 (03) : 300 - 314
  • [46] Chemokine receptor CXCR4 interacts with nuclear receptor Nur77 and promote glioma invasion and progression
    Dai, Yuxiang
    Yu, Chen
    Zhou, Lu
    Cheng, Longyang
    Ni, Hongbin
    Liang, Weibang
    BRAIN RESEARCH, 2024, 1822
  • [47] CXC chemokine receptor 4 (CXCR4) functions as a lactoferrin receptor in macrophages
    Takayama, Y.
    Aoki, R.
    FEBS OPEN BIO, 2018, 8 : 376 - 376
  • [48] The Clinical Implications of Chemokine Receptor CXCR4 in Grade and Prognosis of Glioma Patients: A Meta-Analysis
    Shunzeng Lv
    Bowen Sun
    Xiao Zhong
    Congxin Dai
    Weiping Wang
    Xiaochen Ma
    Huishu Song
    Ranran Shi
    Renzhi Wang
    Molecular Neurobiology, 2015, 52 : 555 - 561
  • [49] The Clinical Implications of Chemokine Receptor CXCR4 in Grade and Prognosis of Glioma Patients: A Meta-Analysis
    Lv, Shunzeng
    Sun, Bowen
    Zhong, Xiao
    Dai, Congxin
    Wang, Weiping
    Ma, Xiaochen
    Song, Huishu
    Shi, Ranran
    Wang, Renzhi
    MOLECULAR NEUROBIOLOGY, 2015, 52 (01) : 555 - 561
  • [50] Tumor necrosis factor α leads to increased cell surface expression of the chemokine receptor CXCR4 in SKNMC cells
    Rostasy, K
    Kleyner, Y
    Gorgun, G
    Navia, B
    ANNALS OF NEUROLOGY, 2000, 48 (03) : 549 - +