Chemokine Receptors as Targets for Cancer Therapy

被引:63
作者
Wu, Xuesong [1 ]
Lee, Vivian C. [1 ]
Chevalier, Eric [2 ]
Hwang, Sam T. [1 ]
机构
[1] NCI, Dermatol Branch, Bethesda, MD 20892 USA
[2] Polyphor Ltd, CH-4123 Allschwil, Switzerland
关键词
CELL LUNG-CANCER; LYMPH-NODE METASTASIS; LIGAND BIOLOGICAL AXIS; REGULATORY T-CELLS; B16; TUMOR-CELLS; GROWTH-FACTOR; IN-VITRO; FRACTALKINE RECEPTOR; LEUKOCYTE MIGRATION; STROMAL FIBROBLASTS;
D O I
10.2174/138161209787582165
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Chemokines and their receptors play critical roles in leukocyte trafficking during inflammatory processes. Although the role of chemokine receptors (CKRs) in cancer biology is a relatively new field of study, a growing body of data suggest that a number of CKRs, including CXCR4, CCR4, CCR7, and CCR10, may play diverse of roles in cancer growth, cancer metastasis, cancer angiogenesis, or the composition of the cancer microenvironment. Preclinical models of cancer indicate that cancer antagonists, most notably those for CXCR4, can block cancer growth either directly or by altering the cancer stroma. Highthroughput screening methods to identify effective CKR antagonists have been developed, but specificity, potency, and drug-delivery of validated candidate compounds remain issues that result in the clinical failure of many initially promising candidates. The recent approval of a CCR5 receptor antagonist in HIV suggests that safe, effective small molecular antagonists for other CKRs may not be far away. There is still a clear need to extend our understanding of the signalling pathways by which CKRs facilitate cancer processes. Because of the role of CKRs in cancer cell survival, the combination of CKR antagonists with traditional chemotoxic agents or with immunotherapy is an alluring strategy since this increases the specificity of treatment to the cancer and potentially limits additional systemic side effects.
引用
收藏
页码:742 / 757
页数:16
相关论文
共 142 条
  • [1] Guide to receptors and channels (GRAC), 3rd edition
    Alexander, Stephen P. H.
    Mathie, Alistair
    Peters, John A.
    [J]. BRITISH JOURNAL OF PHARMACOLOGY, 2008, 153 : S1 - S209
  • [2] Cross-talk between paracrine-acting cytokine and chemokine pathways promotes malignancy in benign human prostatic
    Ao, Mingfang
    Franco, Omar E.
    Park, Dean
    Raman, Dayanidhi
    Williams, Karin
    Hayward, Simon W.
    [J]. CANCER RESEARCH, 2007, 67 (09) : 4244 - 4253
  • [3] Interleukin-8 is a molecular determinant of androgen independence and progression in prostate cancer
    Araki, Shinako
    Omori, Yohei
    Lyn, Dominic
    Singh, Rajendra K.
    Meinbach, David M.
    Sandman, Yekutiel
    Lokeshwar, Vinata B.
    Lokeshwar, Bal L.
    [J]. CANCER RESEARCH, 2007, 67 (14) : 6854 - 6862
  • [4] Inhibition of interleukin-8 reduces tumorigenesis of human non-small cell lung cancer in SCID mice
    Arenberg, DA
    Kunkel, SL
    Polverini, PJ
    Glass, M
    Burdick, MD
    Strieter, RM
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (12) : 2792 - 2802
  • [5] ARONICA SM, 2008, J INTERFERON CYTOKIN
  • [6] NEUTROPHIL-ACTIVATING PEPTIDE-1 INTERLEUKIN-8, A NOVEL CYTOKINE THAT ACTIVATES NEUTROPHILS
    BAGGIOLINI, M
    WALZ, A
    KUNKEL, SL
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (04) : 1045 - 1049
  • [7] Chemokines and leukocyte traffic
    Baggiolini, M
    [J]. NATURE, 1998, 392 (6676) : 565 - 568
  • [8] Balch Charles M, 2003, Semin Surg Oncol, V21, P43, DOI 10.1002/ssu.10020
  • [9] In silico identified CCR4 antagonists target regulatory T cells and exert adjuvant activity in vaccination
    Bayry, Jagadeesh
    Tchilian, Elma Z.
    Davies, Matthew N.
    Forbes, Emily K.
    Draper, Simon J.
    Kaveri, Srini V.
    Hill, Adrian V. S.
    Kazatchkine, Michel D.
    Beverley, Peter C. L.
    Flower, Darren R.
    Tough, David F.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (29) : 10221 - 10226
  • [10] Organ selectivity in metastasis: regulation by chemokines and their receptors
    Ben-Baruch, Adit
    [J]. CLINICAL & EXPERIMENTAL METASTASIS, 2008, 25 (04) : 345 - 356