Regulative role of the CXCL13-CXCR5 axis in the tumor microenvironment

被引:24
作者
Tan, Ping [1 ]
Shi, Ming [1 ]
Lai, Li [2 ]
Tang, Zhuang [1 ]
Xie, Nan [3 ]
Xu, Hang [1 ]
Wei, Qiang [1 ]
Zhang, Xiaoyu [4 ]
Yang, Lu [1 ]
Wu, Lily [4 ,5 ]
机构
[1] Sichuan Univ, West China Hosp, Inst Urol, Dept Urol, Chengdu, Sichuan, Peoples R China
[2] Sichuan Univ, West China Hosp, Ctr Anesthesiol & Surg, Chengdu, Sichuan, Peoples R China
[3] Sichuan Univ, West China Hosp, Dept Emergency, Chengdu, Sichuan, Peoples R China
[4] Univ Calif Los Angeles, David Geffen Sch Med, Dept Mol & Med Pharmacol, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, David Geffen Sch Med, Dept Urol, Los Angeles, CA 90095 USA
基金
中国国家自然科学基金;
关键词
chemokine; CXCL13; CXCR5; tumor; microenvironment;
D O I
10.1093/pcmedi/pby006
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Chemokines are best known for their abilities of recruiting immune cells and forming lymphoid tissue. Through interactions between chemokines and their receptors, various immune cell subsets are recruited into the tumor microenvironment which is the primary location for tumor cells interacting with responding host cells. In recent decades, a large volume of studies have revealed chemokines' role in the tumor microenvironment in regulating tumor growth, invasion, and/or metastasis as well as tumor immune response; however, their molecular mechanisms are not well understood. Recently, increasing evidence has reported the importance of the CXCL13-CXCR5 axis in the tumor microenvironment of various human malignancies. Thus, in this review, we will focus on the CXCL13-CXCR5 axis and elaborate on the expression patterns, regulating and corresponding regulatory mechanisms as well as clinical values in a wide range of human cancers.
引用
收藏
页码:49 / 56
页数:8
相关论文
共 85 条
[1]  
Amedei A, 2013, RECENT PAT ANTI-CANC, V8, P126
[2]   Tissue injury and hypoxia promote malignant progression of prostate cancer by inducing CXCL13 expression in tumor myofibroblasts [J].
Ammirante, Massimo ;
Shalapour, Shabnam ;
Kang, Youngjin ;
Jamieson, Christina A. M. ;
Karin, Michael .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2014, 111 (41) :14776-14781
[3]   B-cell-derived lymphotoxin promotes castration-resistant prostate cancer [J].
Ammirante, Massimo ;
Luo, Jun-Li ;
Grivennikov, Sergei ;
Nedospasov, Sergei ;
Karin, Michael .
NATURE, 2010, 464 (7286) :302-U187
[4]   CXCR5+ CD8+ T cells potently infiltrate pancreatic tumors and present high functionality [J].
Bai, Minghui ;
Zheng, Youwei ;
Liu, Haichao ;
Su, Baowei ;
Zhan, Yong ;
He, Hua .
EXPERIMENTAL CELL RESEARCH, 2017, 361 (01) :39-45
[5]   Cancer and the chemokine network [J].
Balkwill, F .
NATURE REVIEWS CANCER, 2004, 4 (07) :540-550
[6]   CXCL13-CXCR5 co-expression regulates epithelial to mesenchymal transition of breast cancer cells during lymph node metastasis [J].
Biswas, Subir ;
Sengupta, Suman ;
Chowdhury, Sougata Roy ;
Jana, Samir ;
Mandal, Gunjan ;
Mandal, Palash Kumar ;
Saha, Nipun ;
Malhotra, Vivek ;
Gupta, Arnab ;
Kuprash, Dmitry V. ;
Bhattacharyya, Arindam .
BREAST CANCER RESEARCH AND TREATMENT, 2014, 143 (02) :265-276
[7]   The expression of CXCL13 and its relation to unfavorable clinical characteristics in young breast cancer [J].
Chen, Lujia ;
Huang, Zhongxi ;
Yao, Guangyu ;
Lyu, Xiaoming ;
Li, Jinbang ;
Hu, Xiaolei ;
Cai, Yahong ;
Li, Wenji ;
Ye, Changsheng ;
Li, Xin .
JOURNAL OF TRANSLATIONAL MEDICINE, 2015, 13
[8]   Chemokines and their receptors in lung cancer progression and metastasis [J].
Cheng, Zeng-hui ;
Shi, Yu-xin ;
Yuan, Min ;
Xiong, Dan ;
Zheng, Jiang-hua ;
Zhang, Zhi-yong .
JOURNAL OF ZHEJIANG UNIVERSITY-SCIENCE B, 2016, 17 (05) :342-351
[9]   Chemokines in Cancer [J].
Chow, Melvyn T. ;
Luster, Andrew D. .
CANCER IMMUNOLOGY RESEARCH, 2014, 2 (12) :1125-1131
[10]   Quantifying differential gene connectivity between disease states for objective identification of disease-relevant genes [J].
Chu, Jen-hwa ;
Lazarus, Ross ;
Carey, Vincent J. ;
Raby, Benjamin A. .
BMC SYSTEMS BIOLOGY, 2011, 5