Inhibition of chaetocin on retinoblastoma progression by modulating the miR-124/SBK1 axis

被引:0
|
作者
Sun, Qiaoling [1 ]
Zhao, Xiaozhao [1 ]
Jin, Bei [1 ]
Shu, Baotong [1 ]
Ma, Yu [2 ]
机构
[1] Henan Med Coll, Dept Optometry, Zhengzhou 451191, Henan, Peoples R China
[2] Zhengzhou Univ, Affiliated Hosp 5, Dept Ophthalmol, Zhengzhou 450052, Henan, Peoples R China
关键词
Chaetocin; Retinoblastoma; miR-124; SBK1; Progression; UP-REGULATION; INVASION; CANCER; PROLIFERATION; EPIDEMIOLOGY; APOPTOSIS; GROWTH;
D O I
10.1166/mex.2023.2510
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
We conducted cellular and animal experiments to investigate the correlation between miR-124/SBK1 and retinoblastoma (RB) progression, as well as to elucidate the anti-cancer efficacy of chaetocin in RB. Initially, miR-124 levels showed a significant decrease in RB tissues and cells, which further declined with increasing tumor diameter and clinical stage. In cellular experiments, inhibiting miR-124 expression significantly enhanced the viability and invasiveness of Y79 cells, while up-regulating miR-124 suppressed the malignant biology of Y79 cells by targeting SBK1 levels, thereby reducing their viability and invasiveness. Subsequent animal experiments provided further evidence that SBK1 was the functional target of miR-124, P: 127.0.0.1 On: Tue, 21 Nov 2023 0 :47: 6 and its up-regulation significantly facilitated RB progression. Additionally, chaetocin demonstrated anti-tumor Copyrigh : American Scie tific Publishers Deivered by I g nta effects through the upregulation of miR-124 and downregulation of SBK1. Therefore, chaetocin can effectively inhibit RB progression by targeting the upregulation of miR-124 and downregulation of SBK1.
引用
收藏
页码:2101 / 2109
页数:9
相关论文
共 50 条
  • [1] NEAT1 promotes retinoblastoma progression via modulating miR-124
    Wang, Lufei
    Yang, Defeng
    Tian, Rui
    Zhang, Hui
    JOURNAL OF CELLULAR BIOCHEMISTRY, 2019, 120 (09) : 15585 - 15593
  • [2] Long non-coding RNA UCA1 promotes retinoblastoma progression by modulating the miR-124/c-myc axis
    Wang, Lan
    Wu, Mingxing
    Zhou, Xiyuan
    AMERICAN JOURNAL OF TRANSLATIONAL RESEARCH, 2022, 14 (03): : 1592 - 1605
  • [3] LncRNA ELFN1-AS1 Promotes Retinoblastoma Growth and Invasion via Regulating miR-4270/SBK1 Axis
    Feng, Wanguo
    Zhu, Ruixi
    Ma, Junlong
    Song, Han
    CANCER MANAGEMENT AND RESEARCH, 2021, 13 : 1067 - 1073
  • [4] RETRACTED: Knockdown of lncRNA XIST inhibits retinoblastoma progression by modulating the miR-124/STAT3 axis (Retracted article. See vol. 149, 2022)
    Hu, Chunmei
    Liu, Shu
    Han, Mei
    Wang, Yingxue
    Xu, Chunling
    BIOMEDICINE & PHARMACOTHERAPY, 2018, 107 : 547 - 554
  • [5] Suppression of lncRNA HOXA11-AS/miR-124 Axis Inhibits Glioma Progression
    He, Yishan
    Qiu, Xinguang
    CELL BIOCHEMISTRY AND BIOPHYSICS, 2021, 79 (04) : 815 - 822
  • [6] Dysregulation of the DRAIC/SBK1 Axis Promotes Lung Cancer Progression
    Alhammad, Rashed
    Allison, Milicia
    Alhammad, Fares
    Anene, Chinedu Anthony
    DIAGNOSTICS, 2024, 14 (19)
  • [7] Knockdown of lncRNA HOTTIP Inhibits Retinoblastoma Progression by Modulating the miR-101-3p/STC1 Axis
    Yuan, XiangWen
    Sun, Zhaoyan
    Cui, Congxian
    TECHNOLOGY IN CANCER RESEARCH & TREATMENT, 2021, 20
  • [8] KCNQ1OT1 regulates the retinoblastoma cell proliferation, migration and SIRT1/JNK signaling pathway by targeting miR-124/SP1 axis
    Zhang, Haitao
    Yang, Xin
    Xu, Yingying
    Li, Haijun
    BIOSCIENCE REPORTS, 2021, 41 (01)
  • [9] miR-124 Functions As A Melanoma Tumor Suppressor By Targeting RACK1
    Shen, Congcong
    Hua, Hui
    Gu, Lixiong
    Cao, Shuanglin
    Cai, Hengji
    Yao, Xiaodong
    Chen, Xiaodong
    ONCOTARGETS AND THERAPY, 2019, 12 : 9975 - 9986
  • [10] Suppression of lncRNA HOXA11-AS/miR-124 Axis Inhibits Glioma Progression
    Yishan He
    Xinguang Qiu
    Cell Biochemistry and Biophysics, 2021, 79 : 815 - 822