COUP-TFII promotes epithelial-mesenchymal transition by inhibiting miR-34a expression in colorectal cancer

被引:8
|
作者
Bao, Ying [1 ]
Lu, Yongliang [2 ]
Feng, Wenming [1 ]
Yu, Hongbin [1 ]
Guo, Huihui [1 ]
Tao, Yulong [1 ]
Shi, Qian [1 ]
Chen, Wei [3 ,4 ]
Wang, Xiang [1 ]
机构
[1] Huzhou Univ, Affiliated Hosp 1, Peoples Hosp Huzhou 1, 158 Guangchanghou Rd, Huzhou 313000, Zhejiang, Peoples R China
[2] Huzhou Univ Huzhou, Dept Med, Huzhou 313000, Zhejiang, Peoples R China
[3] Tongde Hosp Zhejiang Prov, Zhejiang Acad Tradit Chinese Med, Canc Inst Integrated Tradit Chinese & Western Med, Key Lab Canc Prevent & Therapy Combining Tradit C, 234 Gucui Rd, Hangzhou 310012, Zhejiang, Peoples R China
[4] Tongde Hosp Zhejiang Prov, Dept Med Oncol, Hangzhou 310012, Zhejiang, Peoples R China
关键词
colorectal cancer; chicken ovalbumin upstream promoter-transcription factor II; microRNA-34a; invasion; migration; epithelial-mesenchymal transition; ORPHAN NUCLEAR RECEPTOR; TRANSCRIPTION FACTOR; CELL-PROLIFERATION; POOR-PROGNOSIS; METASTASIS; GROWTH; KNOCKDOWN; APOPTOSIS; INVASION; NR2F2;
D O I
10.3892/ijo.2019.4718
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chicken ovalbumin upstream promoter-transcription factor II (COUP-TFII) expression is upregulated in colorectal cancer and is associated with its progression and a poor prognosis. The aim of the present study was to determine whether COUP-TFII regulates colorectal cancer cell (CRC) invasion and migration by inhibiting microRNA (miR)-34a. Transwell system and wound healing assays were performed to examine cell invasiveness and migration, respectively. Reverse transcription polymerase chain reaction and western blotting were used to detect the RNA and protein levels of target molecules, respectively. The results revealed that COUP-TFII knockdown significantly inhibited CRC invasion and migration. In addition, the expression of miR-34a, a well-known tumor suppressor was revealed to be inversely correlated with COUP-TFII expression. The miR-34a mimic significantly reduced CRC invasion and migration abilities, while the miR-34a inhibitor enhanced CRC invasion and migration activity. There was no significant difference between the negative small interfering RNA and miR-34a inhibitor groups following knockdown of COUP-TFII. Furthermore, western blotting demonstrated that miR-34a mimics inhibited the epithelial-mesenchymal transition (EMT) process of CRCs, while the miR-34a inhibitor had the opposite effect. Taken together, the results demonstrate that miR-34a regulates CRC invasion and migration by examining the mechanism by which COUP-TFII regulates EMT.
引用
收藏
页码:1337 / 1344
页数:8
相关论文
共 50 条
  • [41] ZAG promotes colorectal cancer cell proliferation and epithelial-mesenchymal transition by promoting lipid synthesis
    Xu, Maotao
    Jin, Xingzheng
    Shen, Zhouli
    OPEN LIFE SCIENCES, 2024, 19 (01):
  • [42] miR-29b suppresses tumor growth and metastasis in colorectal cancer via downregulating Tiam1 expression and inhibiting epithelial-mesenchymal transition
    Wang, B.
    Li, W.
    Liu, H.
    Yang, L.
    Liao, Q.
    Cui, S.
    Wang, H.
    Zhao, L.
    CELL DEATH & DISEASE, 2014, 5 : e1335 - e1335
  • [43] Epithelial-mesenchymal transition promotes SOX2 and NANOG expression in bladder cancer
    Migita, Toshiro
    Ueda, Ayano
    Ohishi, Tomokazu
    Hatano, Megumi
    Seimiya, Hiroyuki
    Horiguchi, Shin-ichiro
    Koga, Fumitaka
    Shibasaki, Futoshi
    LABORATORY INVESTIGATION, 2017, 97 (05) : 567 - 576
  • [44] miR-551b regulates epithelial-mesenchymal transition and metastasis of gastric cancer by inhibiting ERBB4 expression
    Song Guangyuan
    Zhang Hongcheng
    Chen Chenlin
    Gong Lijie
    Chen Biao
    Zhao Shaoyun
    Shi Ji
    Xu Ji
    Ye Zaiyuan
    ONCOTARGET, 2017, 8 (28) : 45725 - 45735
  • [45] Glutamine deficiency promotes recurrence and metastasis in colorectal cancer through enhancing epithelial-mesenchymal transition
    Sun, Hongyan
    Zhang, Chuan
    Zheng, Yang
    Liu, Chenlu
    Wang, Xue
    Cong, Xianling
    JOURNAL OF TRANSLATIONAL MEDICINE, 2022, 20 (01)
  • [46] Peroxiredoxin 5 promotes the epithelial-mesenchymal transition in colon cancer
    Ahn, Hye-Mi
    Yoo, Jin-Woo
    Lee, Seunghoon
    Lee, Hong Jun
    Lee, Hyun-Shik
    Lee, Dong-Seok
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2017, 487 (03) : 580 - 586
  • [47] Cartilage Oligomeric Matrix Protein promotes epithelial-mesenchymal transition by interacting with Transgelin in Colorectal Cancer
    Zhong, Weilong
    Hou, Huiqin
    Liu, Tianyu
    Su, Shuai
    Xi, Xiaonan
    Liao, Yusheng
    Xie, Runxiang
    Jin, Ge
    Liu, Xiang
    Zhu, Lanping
    Zhang, Hongxia
    Song, Xueli
    Yang, Cheng
    Sun, Tao
    Cao, Hailong
    Wang, Bangmao
    THERANOSTICS, 2020, 10 (19): : 8790 - 8806
  • [48] Activation of AKT Signaling Promotes Epithelial-Mesenchymal Transition and Tumor Growth in Colorectal Cancer Cells
    Suman, Suman
    Kurisetty, Vittal
    Das, Trinath P.
    Vadodkar, Aditi
    Ramos, Gabriel
    Lakshmanaswamy, Rajkumar
    Damodaran, Chendil
    MOLECULAR CARCINOGENESIS, 2014, 53 : E151 - E160
  • [49] ATP6L promotes metastasis of colorectal cancer by inducing epithelial-mesenchymal transition
    Wang, Jingyi
    Chen, Dandan
    Song, Wangzhao
    Liu, Zhiyong
    Ma, Wenjuan
    Li, Xiaofeng
    Zhang, Chao
    Wang, Xin
    Wang, Yalei
    Yang, Ye
    Cao, Wenfeng
    Qi, Lisha
    CANCER SCIENCE, 2020, 111 (02) : 477 - 488
  • [50] Role of miR-34a in TGF-β1-and Drug-Induced Epithelial-Mesenchymal Transition in Alveolar Type II Epithelial Cells
    Takano, Mikihisa
    Nekomoto, Chinami
    Kawami, Masashi
    Yumoto, Ryoko
    JOURNAL OF PHARMACEUTICAL SCIENCES, 2017, 106 (09) : 2868 - 2872