Overexpression of HES6 has prognostic value and promotes metastasis via the Wnt/-catenin signaling pathway in colorectal cancer

被引:13
|
作者
Xu, Yuandong [1 ,2 ]
Liu, Xuejuan [1 ]
Zhang, Huizhong [3 ]
Zhu, Ziyuan [1 ]
Wu, Xianqiu [4 ]
Wu, Xiaobing [1 ]
Li, Shuling [1 ]
Song, Libing [4 ,5 ]
Xu, Xuehu [1 ]
机构
[1] Guangzhou Med Univ, Dept Gastrointestinal Surg, Affiliated Hosp 3, 63 Duobao Rd, Guangzhou 510150, Guangdong, Peoples R China
[2] Guangdong Pharmaceut Univ, Dept Gen Surg 2, Affiliated Hosp 1, Sch Clin Med, Guangzhou 510062, Guangdong, Peoples R China
[3] Sun Yat Sen Univ, Dept Pathol, Collaborat Innovat Ctr Canc Med, Canc Ctr,State Key Lab Oncol South China, Guangzhou 510060, Guangdong, Peoples R China
[4] Sun Yat Sen Univ, Dept Expt Res, State Key Lab Oncol South China, Canc Ctr, Guangzhou 510060, Guangdong, Peoples R China
[5] Guangzhou Med Univ, Sch Basic Med Sci, Key Lab Prot Modificat & Degradat, Affiliated Canc Hosp & Inst, Guangzhou 510095, Guangdong, Peoples R China
关键词
colorectal cancer; HES6; prognosis; metastasis; Wnt/beta-catenin; EPITHELIAL-MESENCHYMAL TRANSITION; BETA-CATENIN; CELL-PROLIFERATION; PROSTATE-CANCER; EXPRESSION; GENE; INHIBITOR; CARCINOMA; COMPLEX; GROWTH;
D O I
10.3892/or.2018.6539
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
HES6 is a member of the hairy-enhancer of the split homolog family, which has been implicated in oncogenesis and cancer progression in a variety of human cancers, including prostate and breast cancer. However, its clinical significance and biological role in colorectal cancer (CRC) remain unclear. In the present study, the expression of HES6 was significantly upregulated in CRC cell lines and CRC tissues at both the mRNA and protein levels. The present study also reported high expression of HES6 in 138/213 (64.8%) paraffin-embedded archived CRC specimens. HES6 expression was significantly correlated with T classification (P<0.001), N classification (P=0.020), and distant metastasis (P<0.001). Patients with higher HES6 expression levels exhibited a reduced overall survival (P<0.001). In addition, a multivariate analysis revealed that the expression of HES6 may be a novel prognostic marker for the survival of patients with CRC. Furthermore, the present study demonstrated that ectopic expression of HES6 enhanced the migration and invasive abilities of CRC cells. These abilities were significantly inhibited upon knockdown of endogenous HES6 expression by specific short hairpin RNAs. Additionally, the present study reported that the effects of HES6 on metastasis may be associated with the activation of the Wnt/-catenin signaling pathway. Collectively, the findings of the present study revealed that overexpression of HES6 played a key role in the progression of CRC, leading to a poor prognosis and clinical outcome.
引用
收藏
页码:1261 / 1274
页数:14
相关论文
共 50 条
  • [41] NMIIA promotes tumor growth and metastasis by activating the Wnt/β-catenin signaling pathway and EMT in pancreatic cancer
    Zhou, Pingting
    Li, Yanyan
    Li, Bo
    Zhang, Meichao
    Liu, Yuanhua
    Yao, Yuan
    Li, Dong
    ONCOGENE, 2019, 38 (27) : 5500 - 5515
  • [42] PLAC8 Overexpression Promotes Lung Cancer Cell Growth via Wnt/β-Catenin Signaling
    Chen, Wei
    Wu, Junlu
    Wang, Weiwei
    Yu, Li
    Xu, Xianghuai
    JOURNAL OF IMMUNOLOGY RESEARCH, 2022, 2022
  • [43] MACC1 promotes carcinogenesis of colorectal cancer via β-catenin signaling pathway
    Zhen, Tiantian
    Dai, Sujuan
    Li, Hui
    Yang, Yang
    Kang, Lili
    Shi, Huijuan
    Zhang, Fenfen
    Yang, Dongjie
    Cai, Shirong
    He, Yulong
    Liang, Yingjie
    Han, Anjia
    ONCOTARGET, 2014, 5 (11) : 3756 - 3769
  • [44] TRIM24 promotes the aggression of gastric cancer via the Wnt/β-catenin signaling pathway
    Fang, Ziling
    Deng, Jun
    Zhang, Ling
    Xiang, Xiaojun
    Yu, Feng
    Chen, Jun
    Feng, Miao
    Xiong, Jianping
    ONCOLOGY LETTERS, 2017, 13 (03) : 1797 - 1806
  • [45] LINC00365 promotes colorectal cancer cell progression through the Wnt/β-catenin signaling pathway
    Zhu, Yiping
    Bian, Yinzhu
    Zhang, Qun
    Hu, Jing
    Li, Li
    Yang, Mi
    Qian, Hanqing
    Yu, Lixia
    Liu, Baorui
    Qian, Xiaoping
    JOURNAL OF CELLULAR BIOCHEMISTRY, 2020, 121 (02) : 1260 - 1272
  • [46] Biliverdin Reductase A (BLVRA) Promotes Colorectal Cancer Cell Progression by Activating the Wnt/β-Catenin Signaling Pathway
    Mao, Haiyan
    Xu, Yuan
    Zhang, Zhengrong
    Sun, Guozhuang
    Wang, Zhu
    Qiao, Dawei
    Yin, Xudong
    Liu, Siping
    Bo, Ping
    CANCER MANAGEMENT AND RESEARCH, 2020, 12 : 2697 - 2709
  • [47] CENPA promotes clear cell renal cell carcinoma progression and metastasis via Wnt/β-catenin signaling pathway
    Qi Wang
    Jiaju Xu
    Zhiyong Xiong
    Tianbo Xu
    Jingchong Liu
    Yuenan Liu
    Jiaping Chen
    Jian Shi
    Yi Shou
    Changjie Yue
    Di Liu
    Huageng Liang
    Hongmei Yang
    Xiong Yang
    Xiaoping Zhang
    Journal of Translational Medicine, 19
  • [48] Tumor Endothelial Marker 8 Promotes Proliferation and Metastasis via the Wnt/β-Catenin Signaling Pathway in Lung Adenocarcinoma
    Ding, Chen
    Liu, Jun
    Zhang, Jiali
    Wan, Yang
    Hu, Linhui
    Charwudzi, Alice
    Zhan, Heqin
    Meng, Ye
    Zheng, Huimin
    Wang, HuiPing
    Wang, Youliang
    Gao, Lihua
    Hu, Xianwen
    Li, Jingrong
    Xiong, Shudao
    FRONTIERS IN ONCOLOGY, 2021, 11
  • [49] CENPA promotes clear cell renal cell carcinoma progression and metastasis via Wnt/β-catenin signaling pathway
    Wang, Qi
    Xu, Jiaju
    Xiong, Zhiyong
    Xu, Tianbo
    Liu, Jingchong
    Liu, Yuenan
    Chen, Jiaping
    Shi, Jian
    Shou, Yi
    Yue, Changjie
    Liu, Di
    Liang, Huageng
    Yang, Hongmei
    Yang, Xiong
    Zhang, Xiaoping
    JOURNAL OF TRANSLATIONAL MEDICINE, 2021, 19 (01)
  • [50] FUBP1 promotes colorectal cancer stemness and metastasis via DVL1-mediated activation of Wnt/β-catenin signaling
    Yin, Haofan
    Gao, Tianxiao
    Xie, Jinye
    Huang, Zhijian
    Zhang, Xiaoyan
    Yang, Fengyu
    Qi, Weiwei
    Yang, Zhonghan
    Zhou, Ti
    Gao, Guoquan
    Yang, Xia
    MOLECULAR ONCOLOGY, 2021, 15 (12) : 3490 - 3512