LncRNA SNHG12 promotes the malignant progression of melanoma by targeting miR-199b

被引:0
|
作者
Xie, Yijie [1 ]
Chen, Guangxiong [1 ]
机构
[1] Ningbo Univ, Affiliated Peoples Hosp, Dept Dermatol, Ningbo 315040, Zhejiang, Peoples R China
关键词
Melanoma; lncRNA; SNHG12; miR-199b; CELL-PROLIFERATION; BREAST-CANCER; MIGRATION; INVASION;
D O I
10.21037/atm-22-214
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Melanoma is a type of tumor caused by the malignant transformation of melanocytes, and has a high degree of malignancy. Small nucleolar RNA host gene 12 (SNHG12) plays an important role in a variety of cancers, but its role in melanoma and its mechanisms are still unclear. In this study, we measured the expression of SNHG12 and explored the molecular mechanisms involved in melanoma. Methods: We detected the expression level of SNHG12 in melanoma cell lines, and explored the effect of SNHG12 on the proliferation, migration, and invasion of melanoma cells in vitro. Mechanistic studies explored the regulation of downstream genes by SNHG12. Results: Overexpression of SNHG12 was found in melanoma cell lines, and SNHG12 promoted the proliferation, migration, and invasion of melanoma cells. MiR-199b is a target gene of SNHG12, which was expressed at low levels in melanoma cell lines, and SNHG12 regulated melanoma cell proliferation, migration, and invasion through miR-199b. We also revealed that SNHG12 promoted the expression of the target genes of miR-199b, namely ETS1, PXN,JAG1, and DDR1. Conclusions: SNHG12 is highly expressed in melanoma, and promotes the expression of ETS1, PXN, JAG1, and DDR1 through targeted regulation of miR-199b, thereby promoting the proliferation, migration, and invasion of melanoma cells.
引用
收藏
页数:9
相关论文
共 50 条
  • [21] Long noncoding RNA SNHG12 promotes the progression of cervical cancer via modulating miR-125b/STAT3 axis
    Jin, Xue-J.
    Chen, Xiang-J.
    Zhang, Zhi-F.
    Hu, Wen-S.
    Ou, Rong-Y.
    Li, Shi
    Xue, Ji-S.
    Chen, Lu-L.
    Hu, Yan
    Zhu, Hua
    JOURNAL OF CELLULAR PHYSIOLOGY, 2019, 234 (05) : 6624 - 6632
  • [22] Long Noncoding RNA SNHG14 Promotes Ischemic Brain Injury via Regulating miR-199b/AQP4 Axis
    Zhang, Guanglin
    Li, Tianxiao
    Chang, Xiaozan
    Xing, Jun
    NEUROCHEMICAL RESEARCH, 2021, 46 (05) : 1280 - 1290
  • [23] LncRNA SNHG12 promotes proliferation and migration of hepatic progenitor cells via the Wnt/β-catenin pathway
    Liu, Ping
    Wang, Juanjuan
    Du, Weixing
    Chen, Lianhua
    ADVANCES IN CLINICAL AND EXPERIMENTAL MEDICINE, 2023, 32 (09): : 1017 - 1027
  • [24] Long Noncoding RNA SNHG14 Promotes Ischemic Brain Injury via Regulating miR-199b/AQP4 Axis
    Guanglin Zhang
    Tianxiao Li
    Xiaozan Chang
    Jun Xing
    Neurochemical Research, 2021, 46 : 1280 - 1290
  • [25] LncRNA SNHG3 Promotes Hepatocellular Tumorigenesis by Targeting miR-326
    Zhao, Qian
    Wu, Chensi
    Wang, Jingwen
    Li, Xidong
    Fan, Yuchen
    Gao, Shuai
    Wang, Kai
    TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE, 2019, 249 (01): : 43 - 56
  • [26] Downregulation of lncRNA SNHG12 reversed IGF1R-induced osteosarcoma metastasis and proliferation by targeting miR-195-5p
    Xu, Ning
    Xu, Jiayuan
    Zuo, Zhuan
    Liu, Yang
    Yan, Feng
    Han, Chenglong
    GENE, 2020, 726
  • [27] LncRNA SNHG12 inhibits miR-199a to upregulate SIRT1 to attenuate cerebral ischemia/reperfusion injury through activating AMPK signaling pathway
    Yin, Wei-Lan
    Yin, Wei-Guo
    Huang, Bai-Sheng
    Wu, Li-Xiang
    NEUROSCIENCE LETTERS, 2019, 690 : 188 - 195
  • [28] LncRNA SNHG12/miR-494-3p/CBX3 axis in diffuse large B-cell lymphoma
    Si, Cheng
    Zhang, Wanyong
    Han, Qi
    Zhu, Bisheng
    Zhan, Chengzhi
    MOLECULAR & CELLULAR TOXICOLOGY, 2023, 19 (01) : 53 - 62
  • [29] LncRNA SNHG12/miR-494-3p/CBX3 axis in diffuse large B-cell lymphoma
    Cheng Si
    Wanyong Zhang
    Qi Han
    Bisheng Zhu
    Chengzhi Zhan
    Molecular & Cellular Toxicology, 2023, 19 : 53 - 62
  • [30] SNHG12 Promotes Angiogenesis Following Ischemic Stroke via Regulating miR-150/VEGF Pathway
    Zhao, Mian
    Wang, Jun
    Xi, Xinlong
    Tan, Nan
    Zhang, Li
    NEUROSCIENCE, 2018, 390 : 231 - 240