RETRACTED: MicroRNA-96-5p promotes proliferation, invasion and EMT of oral carcinoma cells by directly targeting FOXF2 (Retracted article. See vol. 11, 2022)

被引:13
作者
Wang, Haiyan [1 ]
Ma, Ning [2 ]
Li, Wenyue [1 ]
Wang, Zuomin [1 ]
机构
[1] Capital Med Univ, Beijing Chaoyang Hosp, Dept Stomatol, Beijing 100020, Peoples R China
[2] Qingdao Municipal Hosp, Dept Stomatol, Qingdao 266011, Peoples R China
来源
BIOLOGY OPEN | 2020年 / 9卷 / 03期
关键词
Oral squamous cell carcinoma; MicroRNA-96-5p; FOXF2; Proliferation; Invasion; MATRIX METALLOPROTEINASES; MESENCHYMAL TRANSITION; CANCER; GROWTH; EXPRESSION; APOPTOSIS;
D O I
10.1242/bio.049478
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Recently, microRNA-96-5p (miR-96-5p) has been reported to function as both a tumor suppressor and oncogene in several cancer types, including gastric cancer, hepatocellular cancer and lung cancer. However, the biological function of miR-96-5p and its precise mechanisms in oral squamous cell carcinoma (OSCC) have not been well clarified. The aim of this study was to study the roles of miR-96-5p/FOXF2 axis in OSCC. In this study, the miR-96-5p level was dramatically enhanced in OSCC tissues and cell lines, and the FOXF2 expression was significantly reduced. In addition, the FOXF2 expression was negatively related to the miR-96-5p level in OSCC tissues. Furthermore, downregulation of miR-96-5p obviously restrained OSCC cell proliferation, invasion and EMT. We confirmed thatmiR-96-5p could directly target FOXF2 by luciferase reporter assay. Moreover, knockdown of FOXF2 also could markedly promote the proliferation, invasion and EMT of OSCC cells. Finally, overexpression of FOXF2 in OSCC cells partially reversed the promoted effects of miR-96-5p mimic. Knockdown of miR-96-5p restrained OSCC cells proliferation, invasion and EMT via regulation of FOXF2.
引用
收藏
页数:11
相关论文
共 39 条
  • [1] The functions of animal microRNAs
    Ambros, V
    [J]. NATURE, 2004, 431 (7006) : 350 - 355
  • [2] MicroRNAs: Novel Biomarkers for Human Cancer
    Bartels, Claudine L.
    Tsongalis, Gregory J.
    [J]. CLINICAL CHEMISTRY, 2009, 55 (04) : 623 - 631
  • [3] Axis of evil: molecular mechanisms of cancer metastasis
    Bogenrieder, T
    Herlyn, M
    [J]. ONCOGENE, 2003, 22 (42) : 6524 - 6536
  • [4] FOXF2 suppresses the FOXC2-mediated epithelial mesenchymal transition and multidrug resistance of basal-like breast cancer
    Cai, Jun
    Tian, Ai-Xian
    Wang, Qing-Shan
    Kong, Peng-Zhou
    Du, Xin
    Li, Xiao-Qing
    Feng, Yu-Mei
    [J]. CANCER LETTERS, 2015, 367 (02) : 129 - 137
  • [5] FOXO1 degradation via G9a-mediated methylation promotes cell proliferation in colon cancer
    Chae, Yun-Cheol
    Kim, Ji-Young
    Park, Jin Woo
    Kim, Kee-Beom
    Oh, Hyein
    Lee, Kyung-Hwa
    Seo, Sang-Beom
    [J]. NUCLEIC ACIDS RESEARCH, 2019, 47 (04) : 1692 - 1705
  • [6] miR-125b suppresses oral oncogenicity by targeting the anti-oxidative gene PRXL2A
    Chen, Yi-Fen
    Wei, Yun-Yen
    Yang, Cheng-Chieh
    Liu, Chung-Ji
    Yeh, Li-Yin
    Chou, Chung-Hsien
    Chang, Kuo-Wei
    Lin, Shu-Chun
    [J]. REDOX BIOLOGY, 2019, 22
  • [7] Reassessing epithelial to mesenchymal transition as a prerequisite for carcinoma invasion and metastasis
    Christiansen, Jason J.
    Rajasekaran, Ayyappan K.
    [J]. CANCER RESEARCH, 2006, 66 (17) : 8319 - 8326
  • [8] MicroRNA-370 inhibits the proliferation, invasion and EMT of gastric cancer cells by directly targeting PAQR4
    Feng, Ye
    Sun, Tao
    Yu, Yabo
    Gao, Yongjian
    Wang, Xuefeng
    Chen, Zhi
    [J]. JOURNAL OF PHARMACOLOGICAL SCIENCES, 2018, 138 (02) : 96 - 106
  • [9] Cadherins and Epithelial-to-Mesenchymal Transition
    Gheldof, Alexander
    Berx, Geert
    [J]. MOLECULAR BIOLOGY OF CADHERINS, 2013, 116 : 317 - 336
  • [10] A microRNA polycistron as a potential human oncogene
    He, L
    Thomson, JM
    Hemann, MT
    Hernando-Monge, E
    Mu, D
    Goodson, S
    Powers, S
    Cordon-Cardo, C
    Lowe, SW
    Hannon, GJ
    Hammond, SM
    [J]. NATURE, 2005, 435 (7043) : 828 - 833