The Signaling Duo CXCL12 and CXCR4: Chemokine Fuel for Breast Cancer Tumorigenesis

被引:54
作者
Zielinska, Karolina A. [1 ]
Katanaev, Vladimir L. [1 ,2 ,3 ]
机构
[1] Univ Geneva, Fac Med, Dept Cell Physiol & Metab, Translat Res Ctr Oncohaematol, CH-1211 Geneva, Switzerland
[2] Far Eastern Fed Univ, Sch Biomed, Vladivostok 690090, Russia
[3] Minjiang Univ, Inst Oceanog, Fuzhou 350108, Peoples R China
关键词
breast cancer; chemokines; chemokine receptors; CXCL12; CXCR4; SDF1; RECEPTOR CXCR4; CELL-MIGRATION; TUMOR-GROWTH; CXCR4/CXCL12; AXIS; PROMOTES BREAST; G-PROTEINS; METASTASIS; ACTIVATION; INHIBITION; EXPRESSION;
D O I
10.3390/cancers12103071
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Breast cancer remains the most common malignancy in women. In this review, we explore the role of the CXCL12/CXCR4 pathway in breast cancer. We show that the CXCL12/CXCR4 cascade is involved in nearly every aspect of breast cancer tumorigenesis including proliferation, cell motility and distant metastasis. Moreover, we summarize current knowledge about the CXCL12/CXCR4-targeted therapies. Due to the critical roles of this pathway in breast cancer and other malignancies, we believe that audiences in different fields will find this overview helpful. The CXCL12/CXCR4 signaling pathway has emerged in the recent years as a key player in breast cancer tumorigenesis. This pathway controls many aspects of breast cancer development including cancer cell proliferation, motility and metastasis to all target organs. Moreover, the CXCL12/CXCR4 cascade affects both immune and stromal cells, creating tumor-supporting microenvironment. In this review, we examine state-of-the-art knowledge about detrimental roles of the CXCL12/CXCR4 signaling, discuss its therapeutic potential and suggest further research directions beneficial both for basic research and personalized medicine in breast cancer.
引用
收藏
页码:1 / 21
页数:21
相关论文
共 146 条
[1]   Fibroblast-derived CXCL12 promotes breast cancer metastasis by facilitating tumor cell intravasation [J].
Ahirwar, Dinesh K. ;
Nasser, Mohd W. ;
Ouseph, Madhu M. ;
Elbaz, Mohamad ;
Cuitino, Maria C. ;
Kladney, Raleigh D. ;
Varikuti, Sanjay ;
Kaul, Kirti ;
Satoskar, Abhay R. ;
Ramaswamy, Bhuvaneswari ;
Zhang, Xiaoli ;
Ostrowski, Michael C. ;
Leone, Gustavo ;
Ganju, Ramesh K. .
ONCOGENE, 2018, 37 (32) :4428-4442
[2]   Towards the first targeted therapy for triple-negative breast cancer: Repositioning of clofazimine as a chemotherapy-compatible selective Wnt pathway inhibitor [J].
Ahmed, Kamal ;
Koval, Alexey ;
Xu, Jiabin ;
Bodmer, Alexandre ;
Katanaev, Vladimir L. .
CANCER LETTERS, 2019, 449 :45-55
[3]   Multi-stage inhibition in breast cancer metastasis by orally active triple conjugate, LHTD4 (low molecular weight heparin-taurocholate-tetrameric deoxycholate) [J].
Alam, Farzana ;
Al-Hilal, Taslim A. ;
Park, Jooho ;
Choi, Jeong Uk ;
Mahmud, Foyez ;
Jeong, Jee-Heon ;
Kim, In-San ;
Kim, Sang Yoon ;
Hwang, Seung Rim ;
Byun, Youngro .
BIOMATERIALS, 2016, 86 :56-67
[4]   Chemokines: novel targets for breast cancer metastasis [J].
Ali, Simi ;
Lazennec, Gwendal .
CANCER AND METASTASIS REVIEWS, 2007, 26 (3-4) :401-420
[5]   A Unidirectional Transition from Migratory to Perivascular Macrophage Is Required for Tumor Cell Intravasation [J].
Arwert, Esther N. ;
Harney, Allison S. ;
Entenberg, David ;
Wang, Yarong ;
Sahai, Erik ;
Pollard, Jeffrey W. ;
Condeelis, John S. .
CELL REPORTS, 2018, 23 (05) :1239-1248
[6]   Epithelial-to-mesenchymal transition in FHC-silenced cells: the role of CXCR4/CXCL12 axis [J].
Aversa, I. ;
Zolea, F. ;
Ierano, C. ;
Bulotta, S. ;
Trotta, A. M. ;
Faniello, M. C. ;
De Marco, C. ;
Malanga, D. ;
Biamonte, F. ;
Viglietto, G. ;
Cuda, G. ;
Scala, S. ;
Costanzo, F. .
JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, 2017, 36
[7]   The chemokine SDF-1/CXCL12 binds to and signals through the orphan receptor RDC1 in T lymphocytes [J].
Balabanian, K ;
Lagane, B ;
Infantino, S ;
Chow, KYC ;
Harriague, J ;
Moepps, B ;
Arenzana-Seisdedos, F ;
Thelen, M ;
Bachelerie, F .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (42) :35760-35766
[8]   Cancer and the chemokine network [J].
Balkwill, F .
NATURE REVIEWS CANCER, 2004, 4 (07) :540-550
[9]   Multiple myeloma cells recruit tumor-supportive macrophages through the CXCR4/CXCL12 axis and promote their polarization toward the M2 phenotype [J].
Beider, Katia ;
Bitner, Hanna ;
Leiba, Merav ;
Gutwein, Odit ;
Koren-Michowitz, Maya ;
Ostrovsky, Olga ;
Abraham, Michal ;
Wald, Hanna ;
Galun, Eithan ;
Peled, Amnon ;
Nagler, Arnon .
ONCOTARGET, 2014, 5 (22) :11283-11296
[10]   G Protein Coupled Receptor Kinase 3 Regulates Breast Cancer Migration, Invasion, and Metastasis [J].
Billard, Matthew J. ;
Fitzhugh, David J. ;
Parker, Joel S. ;
Brozowski, Jaime M. ;
McGinnis, Marcus W. ;
Timoshchenko, Roman G. ;
Serafin, Stephen ;
Lininger, Ruth ;
Klauber-Demore, Nancy ;
Sahagian, Gary ;
Truong, Young K. ;
Sassano, Maria F. ;
Serody, Jonathan S. ;
Tarrant, Teresa K. .
PLOS ONE, 2016, 11 (04)