Elevated expression of CXCL16 correlates with poor prognosis in patients with colorectal cancer

被引:4
作者
Chen, Zhihui [1 ]
Dai, Weigang [1 ]
Yang, Liang [1 ]
Yang, Hong [2 ]
Ding, Li [3 ]
He, Yulong [1 ]
Song, Xinming [1 ]
Cui, Ji [1 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Gastrointestinal Surg Ctr, Guangzhou 510080, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Operating Dept, Affiliated Hosp 1, Guangzhou 510080, Guangdong, Peoples R China
[3] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Pathol, Guangzhou 510080, Guangdong, Peoples R China
来源
CANCER MANAGEMENT AND RESEARCH | 2019年 / 11卷
关键词
colorectal neoplasms; chemokine; CXCL16; prognosis; CHEMOKINE LIGAND 16; TNF-ALPHA; METASTASIS;
D O I
10.2147/CMAR.S197354
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aims: To examine the expression of CXCL16 in colorectal cancer (CRC) tissue and to clarify the relationships between CXCL16 and clinicopathological features and survival in CRC. Methods: A total of 142 consecutive CRC patients undergoing colorectal surgery at the Department of Gastrointestinal Center, First Affiliated Hospital, Sun Yat-sen University, between January 2010 and December 2010 were enrolled in this study. CXCL16 was measured by immunohistochemical staining in CRC tissue. Association between CXCL16 expression and clinicopathologic parameters was analyzed with a chi-square test. Survival curves were calculated by the Kaplan-Meier method, and the differences between CXCL16 high-and low-expression groups were analyzed using the log-rank test. Cox univariate and multivariate analyses were used to determine risk factors for overall survival (OS). Results: CXCL16 expression was elevated in CRC. CXCL16-positive expression was significantly related to tumor size (P=0.043), tumor differentiation (P=0.046) and distant metastasis (P=0.038), and there was a trend toward lymph node metastasis (P=0.070). CXCL16 expression, together with differentiation, depth of invasion, lymph node metastasis, and distant metastasis, was a significant independent prognostic factor for OS of patients with CRC (HR 2.026, 95% CI 1.128-3.640, P=0.018). Conclusion: CXCL16 expression was enhanced in CRC tissue and was negatively correlated with survival in CRC patients. Furthermore, CXCL16-positive expression was an independent prognostic factor for CRC patients, whilst the underlying mechanisms remain unclear; thus, further studies are needed.
引用
收藏
页码:4691 / 4697
页数:7
相关论文
共 19 条
  • [1] The transmembrane CXC-chemokine ligand 16 is induced by IFN-γ and TNF-α and shed by the activity of the disintegrin-like metalloproteinase ADAM10
    Abel, S
    Hundhausen, C
    Mentlein, R
    Schulte, A
    Berkhout, TA
    Broadway, N
    Hartmann, D
    Sedlacek, R
    Dietrich, S
    Muetze, B
    Schuster, B
    Kallen, KJ
    Saftig, P
    Rose-John, S
    Ludwig, A
    [J]. JOURNAL OF IMMUNOLOGY, 2004, 172 (10) : 6362 - 6372
  • [2] Human brain metastatic stroma attracts breast cancer cells via chemokines CXCL16 and CXCL12
    Chung, Brile
    Esmaeili, Ali A.
    Gopalakrishna-Pillai, Sailesh
    Murad, John P.
    Andersen, Emily S.
    Reddy, Naveen Kumar
    Srinivasan, Gayathri
    Armstrong, Brian
    Chu, Caleb
    Kim, Young
    Tong, Tommy
    Waisman, James
    Yim, John H.
    Badie, Behnam
    Lee, Peter P.
    [J]. NPJ BREAST CANCER, 2017, 3
  • [3] "Inverse signaling" of the transmembrane chemokine CXCL16 contributes to proliferative and anti-apoptotic effects in cultured human meningioma cells
    Hattermann, Kirsten
    Bartsch, Kareen
    Gebhardt, Henrike H.
    Mehdorn, H. Maximilian
    Synowitz, Michael
    Schmitt, Anne Dorothee
    Mentlein, Rolf
    Held-Feindt, Janka
    [J]. CELL COMMUNICATION AND SIGNALING, 2016, 14 : 1 - 11
  • [4] High-level expression of chemokine CXCL16 by tumor cells correlates with a good prognosis and increased tumor-infiltrating lymphocytes in colorectal cancer
    Hojo, Shozo
    Koizumi, Keiichi
    Tsuneyama, Koichi
    Arita, Yoshihisa
    Cui, Zhengguo
    Shinohara, Kanna
    Minami, Takayuki
    Hashimoto, Isaya
    Nakayama, Takashi
    Sakurai, Hiroaki
    Takano, Yasuo
    Yoshie, Osamu
    Tsukada, Kazuhiro
    Saiki, Ikuo
    [J]. CANCER RESEARCH, 2007, 67 (10) : 4725 - 4731
  • [5] Association between CXCL16/CXCR6 expression and the clinicopathological features of patients with non-small cell lung cancer
    Ke, Chuangwu
    Ren, Yanchen
    Lv, Lu
    Hu, Weidong
    Zhou, Wenhui
    [J]. ONCOLOGY LETTERS, 2017, 13 (06) : 4661 - 4668
  • [6] CXCL16 suppresses liver metastasis of colorectal cancer by promoting TNF-α-induced apoptosis by tumor-associated macrophages
    Kee, Ji-Ye
    Ito, Aya
    Hojo, Shozo
    Hashimoto, Isaya
    Igarashi, Yoshiko
    Tsuneyama, Koichi
    Tsukada, Kazuhiro
    Irimura, Tatsuro
    Shibahara, Naotoshi
    Takasaki, Ichiro
    Inujima, Akiko
    Nakayama, Takashi
    Yoshie, Osamu
    Sakurai, Hiroaki
    Saiki, Ikuo
    Koizumi, Keiichi
    [J]. BMC CANCER, 2014, 14
  • [7] Loss of Myosin Vb in colorectal cancer is a strong prognostic factor for disease recurrence
    Letellier, Elisabeth
    Schmitz, Martine
    Ginolhac, Aurelien
    Rodriguez, Fabien
    Ullmann, Pit
    Qureshi-Baig, Komal
    Frasquilho, Sonia
    Antunes, Laurent
    Haan, Serge
    [J]. BRITISH JOURNAL OF CANCER, 2017, 117 (11) : 1689 - 1701
  • [8] High CXC Chemokine Ligand 16 (CXCL16) Expression Promotes Proliferation and Metastasis of Lung Cancer via Regulating the NF-κB Pathway
    Liang, Kun
    Liu, Yanru
    Eer, Dun
    Liu, Jingbin
    Yang, Fan
    Hu, Ke
    [J]. MEDICAL SCIENCE MONITOR, 2018, 24 : 405 - 411
  • [9] Cancer-associated fibroblasts promote hepatocellular carcinoma metastasis through chemokine-activated hedgehog and TGF-β pathways
    Liu, Jiao
    Chen, Sheng
    Wang, Wei
    Ning, Bei-Fang
    Chen, Fei
    Shen, Weifeng
    Ding, Jin
    Chen, Wansheng
    Xie, Wei-Fen
    Zhang, Xin
    [J]. CANCER LETTERS, 2016, 379 (01) : 49 - 59
  • [10] Loss of ZG16 is associated with molecular and clinicopathological phenotypes of colorectal cancer
    Meng, Hui
    Li, Wencai
    Boardman, Lisa A.
    Wang, Liang
    [J]. BMC CANCER, 2018, 18