METTL3 Promotes the Growth and Invasion of Melanoma Cells by Regulating the lncRNA SNHG3/miR-330-5p Axis.

IF 3.2 4区 医学 Q3 CELL & TISSUE ENGINEERING Cell Transplantation Pub Date : 2023-01-01 DOI:10.1177/09636897231188300
Shaojun Chu, Yulong Li, Baojin Wu, Guo Rong, Qiang Hou, Qin Zhou, Dexiang Du, Yufei Li
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Abstract

Accumulating evidence indicates that m6A methyltransferase 3 (METTL3) plays a pivotal role in different malignancies including melanoma. However, the function and underlying mechanisms by which METTL3 contributes to the tumorigenesis of melanoma remain undocumented. The association of METTL3 and long noncoding RNA (lncRNA) small nucleolar RNA host gene 3 (SNHG3) with clinicopathological characteristics and prognosis in patients with melanoma was analyzed by real-time quantitative polymerase chain reaction (RT-qPCR), Western blotting, and The Cancer Genome Atlas data sets. The role of METTL3 in melanoma cells was assessed by in vitro and in vivo experiments. The m6A dot blot, methylated RNA immunoprecipitation (MeRIP), and RT-qPCR were used to verify METTL3-mediated m6A modification of lncRNA SNHG3. The effect of METTL3 on lncRNA SNHG3 was determined by luciferase gene reporter assay, RT-qPCR, and Western blotting. We found that METTL3 was upregulated in melanoma tissue samples and associated with poor survival in patients with melanoma. Knockdown of METTL3 suppressed the growth and invasion of melanoma cells in vitro and in vivo, whereas restored expression of METTL3 promoted these effects. Mechanistic investigations showed that knockdown of METTL3 reduced SNHG3 m6A levels and its messenger ribonucleic acid (mRNA) expression levels. SNHG3 could act as a sponge of microRNA (miR)-330-5p to upregulate the expression of CCHC-type zinc finger nucleic acid binding protein (CNBP). SNHG3 overexpression reversed METTL3-knockdown-caused antitumor effects, miR-330-5p upregulation and CNBP downregulation. SNHG3 had a positive correlation with METTL3 expression but a negative correlation with miR-330-5p expression in melanoma tissue samples. In conclusion, our findings demonstrated that METTL3-mediated m6A modification of lncRNA SNHG3 promoted the growth and invasion of melanoma cells by regulating the miR-330-5p/CNBP axis.

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METTL3通过调节lncRNA SNHG3/miR-330-5p轴促进黑色素瘤细胞的生长和侵袭。
越来越多的证据表明,m6A甲基转移酶3(METTL3)在包括黑色素瘤在内的各种恶性肿瘤中发挥着关键作用。然而,METTL3参与黑色素瘤肿瘤发生的功能和潜在机制尚未得到证实。通过实时定量聚合酶链反应(RT-qPCR)、蛋白质印迹和癌症基因组图谱数据集分析了METTL3和长非编码RNA(lncRNA)小核仁RNA宿主基因3(SNHG3)与黑色素瘤患者的临床病理特征和预后的关系。通过体外和体内实验评估METTL3在黑色素瘤细胞中的作用。m6A点杂交、甲基化RNA免疫沉淀(MeRIP)和RT-qPCR用于验证METTL3介导的lncRNA SNHG3的m6A修饰。METTL3对lncRNA SNHG3的影响通过荧光素酶基因报告子分析、RT-qPCR和蛋白质印迹来确定。我们发现METTL3在黑色素瘤组织样本中上调,并与黑色素瘤患者的低生存率有关。敲除METTL3在体外和体内抑制黑色素瘤细胞的生长和侵袭,而恢复METTL3的表达促进了这些作用。机制研究表明,敲低METTL3降低了SNHG3 m6A水平及其信使核糖核酸(mRNA)表达水平。SNHG3可以作为微小RNA(miR)-330-5p的海绵,上调CCHC型锌指核酸结合蛋白(CNBP)的表达。SNHG3过表达逆转METTL3敲低引起的抗肿瘤作用、miR-330-5p上调和CNBP下调。在黑色素瘤组织样本中,SNHG3与METTL3表达呈正相关,但与miR-330-5p表达负相关。总之,我们的研究结果表明,METTL3介导的lncRNA SNHG3的m6A修饰通过调节miR-330-5p/CNBP轴来促进黑色素瘤细胞的生长和侵袭。
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来源期刊
Cell Transplantation
Cell Transplantation 生物-细胞与组织工程
CiteScore
6.00
自引率
3.00%
发文量
97
审稿时长
6 months
期刊介绍: Cell Transplantation, The Regenerative Medicine Journal is an open access, peer reviewed journal that is published 12 times annually. Cell Transplantation is a multi-disciplinary forum for publication of articles on cell transplantation and its applications to human diseases. Articles focus on a myriad of topics including the physiological, medical, pre-clinical, tissue engineering, stem cell, and device-oriented aspects of the nervous, endocrine, cardiovascular, and endothelial systems, as well as genetically engineered cells. Cell Transplantation also reports on relevant technological advances, clinical studies, and regulatory considerations related to the implantation of cells into the body in order to provide complete coverage of the field.
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