Cytokines and Chemokines as Mediators of Prostate Cancer Metastasis

被引:131
作者
Adekoya, Timothy O. [1 ]
Richardson, Ricardo M. [2 ]
机构
[1] North Carolina Cent Univ, Julius L Chambers Biomed Biotechnol Inst, Durham, NC 27707 USA
[2] North Carolina Cent Univ, Dept Biol & Biomed Sci, Durham, NC 27707 USA
基金
美国国家卫生研究院;
关键词
prostate cancer; metastasis; cytokines; chemokines; ENDOTHELIAL-GROWTH-FACTOR; EPITHELIAL-MESENCHYMAL TRANSITION; NF-KAPPA-B; RECEPTOR CXCR4 EXPRESSION; TGF-BETA; BONE METASTASIS; ANDROGEN RECEPTOR; SIGNAL-TRANSDUCTION; CELL-MIGRATION; TUMOR-GROWTH;
D O I
10.3390/ijms21124449
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
The consequences of prostate cancer metastasis remain severe, with huge impact on the mortality and overall quality of life of affected patients. Despite the convoluted interplay and cross talk between various cell types and secreted factors in the metastatic process, cytokine and chemokines, along with their receptors and signaling axis, constitute important factors that help drive the sequence of events that lead to metastasis of prostate cancer. These proteins are involved in extracellular matrix remodeling, epithelial-mesenchymal-transition, angiogenesis, tumor invasion, premetastatic niche creation, extravasation, re-establishment of tumor cells in secondary organs as well as the remodeling of the metastatic tumor microenvironment. This review presents an overview of the main cytokines/chemokines, including IL-6, CXCL12, TGF beta, CXCL8, VEGF, RANKL, CCL2, CX3CL1, IL-1, IL-7, CXCL1, and CXCL16, that exert modulatory roles in prostate cancer metastasis. We also provide extensive description of their aberrant expression patterns in both advanced disease states and metastatic sites, as well as their functional involvement in the various stages of the prostate cancer metastatic process.
引用
收藏
页码:1 / 29
页数:29
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