miR-150-5p represses TP53 tumor suppressor gene to promote proliferation of colon adenocarcinoma

被引:44
|
作者
Liu, Fang [1 ]
Wang, Xiao Di [1 ]
机构
[1] China Japan Friendship Hosp, Dept Gastroenterol, East St Yinghua, Beijing 100029, Peoples R China
关键词
CANCER; MICRORNA; APOPTOSIS; MELANOMA;
D O I
10.1038/s41598-019-43231-5
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
MicroRNAs (miRNAs) play a critical role in regulation of numerous biological processes and pathogenesis of a variety of diseases. In addition, miRNAs contribute to carcinogenesis by acting as oncogenic or tumor suppressive. Circulating miRNAs including miR-150-5p are associated with colorectal cancer progression, and the putative targets of miR-150-5p include tumor suppressor gene, TP53. Here we sought to investigate the role of miR-150-5p-TP53 signaling pathway in proliferation of colon cancer and to determine expression levels of miR-miR-150-5p and TP53 in colon adenocarcinoma and adjacent non-cancerous tissue samples, or in human colon adenocarcinoma cell lines. MTT assay was used to determine proliferation and apoptosis in cell lines. Furthermore, we used Western blot to determine levels of cell cycle regulators with anti-miR-150-5p or apoptosis with overexpression of TP53. Our results show that expression levels of miR-150-5p were significantly elevated in clinical specimens from cancer patients. We further showed that inhibition of miR-150-5p increased TP53, and in turn, suppression of proliferation of colon adenocarcinoma. Moreover, inhibition of miR-150-5p or overexpression of TP53 caused cell arrest or apoptosis in colon adenocarcinoma. Our results support that miR-150-5p-TP53 pathway plays an important role in regulation of proliferation, cell arrest, and apoptosis in colon cancer, and could be an attractive target for therapy.
引用
收藏
页数:7
相关论文
共 50 条
  • [21] miR-150-5p suppresses tumor progression by targeting VEGFA in colorectal cancer
    Chen, Xiaoxiang
    Xu, Xueni
    Pan, Bei
    Zeng, Kaixuan
    Xu, Mu
    Liu, Xiangxiang
    He, Bangshun
    Pan, Yuqin
    Sun, Huiling
    Wang, Shukui
    AGING-US, 2018, 10 (11): : 3421 - 3437
  • [22] Body mass index (BMI) and mutations of tumor suppressor gene p53 (TP53) in patients with urinary bladder cancer
    Ecke, Thorsten H.
    Schlechte, Horst H.
    Gunia, Sven
    Lenk, Severin V.
    Loening, Stefan A.
    UROLOGIC ONCOLOGY-SEMINARS AND ORIGINAL INVESTIGATIONS, 2008, 26 (05) : 470 - 473
  • [23] Analysis of polymorphisms at the tumor suppressor gene p53 (TP53) in contributing to the risk for schizophrenia and its associated neurocognitive deficits
    Papiol, S
    Arias, B
    Barrantes-Vidal, N
    Guitart, M
    Salgado, P
    Catalán, R
    Fañanás, L
    NEUROSCIENCE LETTERS, 2004, 363 (01) : 78 - 80
  • [24] MIAT inhibits proliferation of cervical cancer cells through regulating miR-150-5p
    Yanbin Liu
    Xingzhi Li
    Hui Zhang
    Yali Huang
    Cancer Cell International, 20
  • [25] MIAT inhibits proliferation of cervical cancer cells through regulating miR-150-5p
    Liu, Yanbin
    Li, Xingzhi
    Zhang, Hui
    Huang, Yali
    CANCER CELL INTERNATIONAL, 2020, 20 (01)
  • [26] JMJD3 Is a Potential Tumor Suppressor Gene That Cooperates with TP53 in Chromosome 17p13
    Teoh, Phaik Ju
    Chung, Tae-Hoon
    Sintosebastian, Chirackal
    Fonseca, Rafael
    Chng, Wee Joo
    BLOOD, 2017, 130
  • [27] miR-150-5p affects AS plaque with ASMC proliferation and migration by STAT1
    Bian, Yuan
    Cai, Wenqiang
    Lu, Hongying
    Tang, Shuhong
    Yang, Keqin
    Tan, Yan
    OPEN MEDICINE, 2021, 16 (01): : 1642 - 1652
  • [28] The tumor suppressor gene TP53 - Twenty years (and 10,000 mutations) later
    Hainaut, P
    BULLETIN DU CANCER, 2000, 87 (01) : 11 - 18
  • [29] Mutations in TP53 tumor suppressor gene in wood dust-related sinonasal cancer
    Holmila, Reetta
    Bornholdt, Jette
    Heikkila, Pirjo
    Suitiala, Tuula
    Fevotte, Joelle
    Cyr, Diane
    Hansen, Johnni
    Snellman, Satu-Marja
    Dictor, Michael
    Steiniche, Torben
    Schlunssen, Vivi
    Schneider, Thomas
    Pukkala, Eero
    Savolainen, Kai
    Wolff, Henrik
    Wallin, Hakan
    Luce, Daniele
    Husgafvel-Pursiainen, Kirsti
    INTERNATIONAL JOURNAL OF CANCER, 2010, 127 (03) : 578 - 588
  • [30] Deoxythymidylate kinase (DTYMK) participates in cell cycle arrest to promote pancreatic adenocarcinoma progression regulated by miR-491-5p through TP53 and is associated with tumor immune infiltration
    Bao, Wenguang
    Yang, Haiyan
    Zhou, Shengsheng
    Huang, Fengxiang
    Wei, Zhe
    Peng, Zhigang
    JOURNAL OF GASTROINTESTINAL ONCOLOGY, 2023, 14 (03) : 1546 - 1559