Regulation of Chemokine Expression in the Tumor Microenvironment

被引:31
作者
Gorbachev, Anton V. [1 ]
Fairchild, Robert L. [1 ,2 ,3 ]
机构
[1] Cleveland Clin, Dept Immunol, Cleveland, OH 44195 USA
[2] Cleveland Clin, Glickman Urol Inst, Cleveland, OH 44195 USA
[3] Case Western Reserve Univ, Sch Med, Dept Pathol, Cleveland, OH USA
关键词
chemokines; tumorigenesis; cancer therapy; CANCER-RELATED INFLAMMATION; MESSENGER-RNA STABILITY; HUMAN BREAST-CANCER; T-CELLS; DENDRITIC CELLS; IFN-GAMMA; CXC CHEMOKINES; MURINE MODEL; MELANOMA PROGRESSION; INDUCIBLE PROTEIN-10;
D O I
10.1615/CritRevImmunol.2014010062
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Chemokines are chemotactic cytokines critical for homeostatic and inflammation-induced trafficking of leukocytes during immune responses, hematopoesis, wound healing, and tumorigenesis. Despite three decades of intensive study of the chemokine network, the molecular mechanisms regulating chemokine expression during tumor growth are not well understood. In this review, we focus on the role of chemokines in both tumor growth and antitumor immune responses and on molecular mechanisms employed by tumor cells to regulate chemokine expression in the tumor microenvironment. Multiple mechanisms used by tumors to regulate chemokine production, including those revealed by very recent studies (such as DNA methylation or post-translational nitrosylation of chemokines) are discussed. Concluding the review, we discuss how understanding of these regulatory mechanisms can be used in cancer therapy to suppress tumor growth and/or to promote immune-mediated eradication of tumors.
引用
收藏
页码:103 / 120
页数:18
相关论文
共 113 条
[1]
Suppression of neuroblastoma growth by dipeptidyl peptidase IV: relevance of chemokine regulation and caspase activation [J].
Arscott, W. T. ;
LaBauve, A. E. ;
May, V. ;
Wesley, U. V. .
ONCOGENE, 2009, 28 (04) :479-491
[2]
CCR7 ligands control basal T cell motility within lymph node slices in a phosphoinositide 3-kinase independent manner [J].
Asperti-Boursin, Francois ;
Real, Eliana ;
Bismuth, Georges ;
Trautmann, Alain ;
Donnadieu, Emmanuel .
JOURNAL OF EXPERIMENTAL MEDICINE, 2007, 204 (05) :1167-1179
[3]
Smoldering and polarized inflammation in the initiation and promotion of malignant disease [J].
Balkwill, F ;
Charles, KA ;
Mantovani, A .
CANCER CELL, 2005, 7 (03) :211-217
[4]
Bellocq A, 1998, AM J PATHOL, V152, P83
[5]
CXCR3, a double-edged sword in tumor progression and angiogenesis [J].
Billottet, Clotilde ;
Quemener, Cathy ;
Bikfalvi, Andreas .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2013, 1836 (02) :287-295
[6]
Regulation of chemokine mRNA stability by lipopolysaccharide and IL-10 [J].
Biswas, R ;
Datta, S ;
Das Gupta, J ;
Novotny, M ;
Tebo, J ;
Hamilton, TA .
JOURNAL OF IMMUNOLOGY, 2003, 170 (12) :6202-6208
[7]
Induction of a proinflammatory program in normal human thyrocytes by the RET/PTC1 oncogene [J].
Borrello, MG ;
Alberti, L ;
Fischer, A ;
Degl'Innocenti, D ;
Ferrario, C ;
Gariboldi, M ;
Marchesi, F ;
Allavena, P ;
Greco, A ;
Collini, P ;
Pilotti, S ;
Cassinelli, G ;
Bressan, P ;
Fugazzola, L ;
Mantovani, A ;
Pierotti, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (41) :14825-14830
[8]
Differential Estrogen-Regulation of CXCL12 Chemokine Receptors, CXCR4 and CXCR7, Contributes to the Growth Effect of Estrogens in Breast Cancer Cells [J].
Boudot, Antoine ;
Kerdivel, Gwenneg ;
Habauzit, Denis ;
Eeckhoute, Jerome ;
Le Dily, Francois ;
Flouriot, Gilles ;
Samson, Michel ;
Pakdel, Farzad .
PLOS ONE, 2011, 6 (06)
[9]
Chemokines in hematopoiesis [J].
Broxmeyer, Hal E. .
CURRENT OPINION IN HEMATOLOGY, 2008, 15 (01) :49-58
[10]
Chinni S, 2013, CANCER RES, DOI [10.1158/1541-7786.MCR-12-0705, DOI 10.1158/1541-7786.MCR-12-0705]