C-X-C Motif Chemokine Ligand 14 is a Unique Multifunctional Regulator of Tumor Progression

被引:13
|
作者
Yang, Xiao-Yan [1 ,2 ,3 ]
Ozawa, Shigeyuki [1 ,2 ]
Kato, Yasumasa [4 ]
Maehata, Yojiro [1 ]
Izukuri, Kazuhito [1 ,5 ]
Ikoma, Takeharu [1 ,2 ]
Kanamori, Keisuke [1 ,2 ]
Akasaka, Tetsu [1 ,6 ]
Suzuki, Kenji [2 ]
Iwabuchi, Hiroshi [2 ]
Kurata, Shun-Ichi [1 ]
Katoh, Iyoko [1 ]
Sakurai, Takashi [2 ]
Kiyono, Tohru [7 ]
Hata, Ryu-Ichiro [1 ,2 ]
机构
[1] Kanagawa Dent Univ, Oral Hlth Sci Res Ctr, Grad Sch, Yokosuka, Kanagawa 2388580, Japan
[2] Kanagawa Dent Univ, Grad Sch, Dept Dentomaxillofacial Diag & Treatment, Yokosuka, Kanagawa 2388580, Japan
[3] Nippi Res Inst Biomatrix, 520-11 Kuwabara, Toride, Ibaraki 3020017, Japan
[4] Ohu Univ, Dept Oral Funct & Mol Biol, Sch Dent, Koriyama, Fukushima 9638611, Japan
[5] Kanagawa Dent Univ, Dept Oral Sci, Grad Sch, Yokosuka, Kanagawa 2388580, Japan
[6] Kanagawa Dent Univ, Dept Crit Care Med & Dent, Grad Sch, Yokosuka, Kanagawa 2388580, Japan
[7] Natl Canc Ctr, Div Carcinogenesis & Canc Prevent, Dept Cell Culture Technol, Res Inst, Tokyo 1040045, Japan
基金
日本学术振兴会;
关键词
C-X-C motif chemokine ligand 14; multifunctional tumor suppressor; antimicrobial function; molecular preventive medicine; BRAK/CXCL14; EXPRESSION; MULTISTEP NATURE; GENE-EXPRESSION; CARCINOMA-CELLS; IN-VIVO; CXCL14; SUPPRESSES; GROWTH; CANCER; BRAK;
D O I
10.3390/ijms20081872
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
Cancer is a leading cause of death and disease worldwide, with a tremendous financial impact. Thus, the development of cost-effective novel approaches for suppressing tumor growth and progression is essential. In an attempt to identify the mechanisms responsible for tumor suppression, we screened for molecules downregulated in a cancer progression model and found that the chemokine CXCL14, also called BRAK, was the most significantly downregulated. Increasing the production of CXCL14 protein by transfecting tumor cells with a CXCL14 expression vector and transplanting the cells into the back skin of immunodeficient mice suppressed tumor cell growth compared with that of parental tumor cells, suggesting that CXCL14 suppressed tumor growth in vivo. However, some studies have reported that over-expression of CXCL14, especially in stromal cells, stimulated the progression of tumor formation. Transgenic mice expressing 10-fold more CXCL14 protein than wild-type C57BL/6 mice showed reduced rates of chemical carcinogenesis, transplanted tumor growth, and metastasis without apparent side effects. CXCL14 also acts as an antimicrobial molecule. In this review, we highlight recent studies involving the identification and characterization of CXCL14 in cancer progression and discuss the reasons for the context-dependent effects of CXCL14 on tumor formation.
引用
收藏
页数:13
相关论文
共 50 条
  • [1] Chemokine (C-X-C motif) ligand 1 is associated with tumor progression and poor prognosis in patients with colorectal cancer
    Zhuo, Changhua
    Wu, Xianyi
    Li, Jing
    Hu, Dan
    Jian, Jinliang
    Chen, Changjiang
    Zheng, Xiongwei
    Yang, Chunkang
    BIOSCIENCE REPORTS, 2018, 38
  • [2] Role of C-X-C chemokine ligand 12/C-X-C chemokine receptor 4 in the progression of hepatocellular carcinoma
    Jeng, Kuo-Shyang
    Jeng, Chi-Juei
    Jeng, Wen-Juei
    Chang, Chiung-Fang
    Sheen, I-Shyan
    ONCOLOGY LETTERS, 2017, 14 (02) : 1905 - 1910
  • [3] Antitumor efficacy of C-X-C motif chemokine ligand 14 in hepatocellular carcinoma in vitro and in vivo
    Wang, Weilin
    Huang, Pengfei
    Zhang, Lufei
    Wei, Jianfeng
    Xie, Qingsong
    Sun, Qiang
    Zhou, Xiaohu
    Xie, Haiyang
    Zhou, Lin
    Zheng, Shusen
    CANCER SCIENCE, 2013, 104 (11) : 1523 - 1531
  • [4] Progestin regulates chemokine (C-X-C motif) ligand 14 transcript level in human endometrium
    Mokhtar, Norfilza M.
    Cheng, Ching-wen
    Cook, Emma
    Bielby, Holli
    Smith, Stephen K.
    Charnock-Jones, D. Stephen
    MOLECULAR HUMAN REPRODUCTION, 2010, 16 (03) : 170 - 177
  • [5] Bovine C-X-C Motif Chemokine Ligand 14 Expression Is Regulated by Alternative Polyadenylation and MicroRNAs
    Zhao, Wei
    Liu, Xueyan
    Li, Chengping
    Qin, Xuyong
    Ren, Shizhong
    Cao, Shujun
    Zhou, Guoli
    ANIMALS, 2023, 13 (19):
  • [6] High Levels of Circulating Chemokine (C-X-C motif) Ligand 11 Are Associated with Euthyroid or Subclinically Hypothyroid Autoimmune Thyroiditis and with Chemokine (C-X-C Motif) Ligand 10
    Antonelli, Alessandro
    Ferri, Clodoveo
    Ferrari, Silvia Martina
    Frascerra, Silvia
    Ruffilli, Ilaria
    Caponi, Laura
    Ulisse, Salvatore
    Miccoli, Mario
    Miccoli, Paolo
    Fallahi, Poupak
    JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 2012, 32 (02): : 74 - 80
  • [7] Chemokine (C-X-C motif) ligand (CXCL)10 in autoimmune diseases
    Antonelli, Alessandro
    Ferrari, Silvia Martina
    Giuggioli, Dilia
    Ferrannini, Ele
    Ferri, Clodoveo
    Fallahi, Poupak
    AUTOIMMUNITY REVIEWS, 2014, 13 (03) : 272 - 280
  • [8] Evaluation of the influence of the C-X-C motif chemokine ligand 12/C-X-C chemokine receptor 4 axis on canine mammary gland tumor cell migration
    Kudo, Ayano
    Sawahata, Hiroki
    Yoshimoto, Sho
    Yamauchi, Akinori
    Oshita, Ryo
    Kanai, Eiichi
    Takagi, Satoshi
    JOURNAL OF VETERINARY MEDICAL SCIENCE, 2023, 85 (08): : 837 - 843
  • [9] The dual roles of C-X-C MOTIF chemokine LIGAND 10 in pediatric osteosarcoma
    Chen, Xiang
    Clement, Margaret
    Hicks, John
    Man, Tsz Kwong
    CANCER RESEARCH, 2022, 82 (12)
  • [10] Chemokine (C-X-C motif) ligand 1/chemokine (C-X-C motif) receptor 2 autocrine loop contributes to cellular proliferation, migration and apoptosis in cervical cancer
    Sun, Jiping
    Yuan, Jianrong
    BIOENGINEERED, 2022, 13 (03) : 7579 - 7591