首页> 外文期刊>Thoracic cancer. >Knockdown of long noncoding RNA TP73‐AS1 suppresses the malignant progression of breast cancer cells in vitro through targeting miRNA‐125a‐3p/metadherin axis
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Knockdown of long noncoding RNA TP73‐AS1 suppresses the malignant progression of breast cancer cells in vitro through targeting miRNA‐125a‐3p/metadherin axis

机译:长度非编码RNA TP73-AS1的敲低通过靶向MiRNA-125A-3P / Metadherin轴来抑制体外乳腺癌细胞的恶性进展

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BACKGROUND:TP73 antisense RNA 1 (TP73-AS1) is a long noncoding RNA which has been shown to be involved in the progression of multiple malignant tumors. Previous studies have demonstrated the oncogenic role of TP73-AS1 in breast cancer. However, its molecular mechanism remains largely unknown in breast tumorigenesis.METHODS:Expression of TP63-AS1, miRNA-125a-3p (miR-125a) and metadherin (MTDH) was detected by real-time quantitative PCR and western blotting. The malignancy was evaluated by cell counting kit 8 (CCK-8), transwell assays, flow cytometry and western blotting. The target binding was confirmed by dual luciferase reporter assay. Xenograft tumor model was performed to detect tumor growth in vivo.RESULTS:Expression of TP73-AS1 was higher in breast cancer tissues and cell lines. Biologically, its knockdown could promote cell apoptosis rate, and inhibit proliferative capacity, migration and invasion ability in HCC-70 and MB231 cells, accompanied with higher cleaved caspase 3 level and lower Ki67, N-cadherin and Vimentin level. Moreover, TP73-AS1 downregulation restrained the tumor growth of HCC-70 cells in vivo. Mechanically, TP73-AS1 functioned as a molecular "sponge" for miR-125a to modulate MTDH, a downstream target of miR-125a. Intriguingly, both miR-125a overexpression and MTDH silencing exerted a tumor-suppressive effect in the malignant progression of HCC-70 and MB231 cells, which was counteracted by TP73-AS1 upregulation and miR-125a downregulation, respectively.CONCLUSION:Knockdown of TP73-AS1 inhibited cell proliferation, migration and invasion, but facilitated apoptosis in breast cancer cells in vitro through targeting miR-125a and upregulating MTDH, suggesting a novel TP73-AS1/miR-125a/MTDH pathway in the malignant progression of breast cancer.? 2019 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd.
机译:背景:TP73反义RNA 1(TP73-AS1)是一种长的非编码RNA,已被证明涉及多种恶性肿瘤的进展。以前的研究表明TP73-AS1在乳腺癌中的致癌作用。然而,其分子机制在乳腺癌中仍然很近未知。通过实时定量PCR和Western印迹检测TP63-AS1,MiRNA-125A-3P(MiR-125A)和Metadherin(MTDH)的表达。通过细胞计数试剂盒8(CCK-8),Transwell测定,流式细胞术和Western印迹评估恶性肿瘤。通过双荧光素酶报告总检测结果证实了靶结合。进行异种移植肿瘤模型以检测体内肿瘤生长。结果:乳腺癌组织和细胞系中TP73-AS1的表达较高。在生物学上,其敲低可以促进细胞凋亡率,抑制HCC-70和MB231细胞中的增殖能力,迁移和侵袭能力,伴随着更高的裂解的胱天蛋白酶3水平和下部Ki67,N-Cadherin和Vimentin水平。此外,TP73-AS1下调抑制了体内HCC-70细胞的肿瘤生长。机械地,TP73-AS1用作MIR-125A的分子“海绵”,以调节MTDH,MIR-125A的下游靶。有趣的是,MIR-125A过表达和MTDH沉默在HCC-70和MB231细胞的恶性进展中发挥了肿瘤抑制作用,其分别抵消了TP73-AS1上调和MIR-125A下调。结论:TP73的敲低 - AS1抑制细胞增殖,迁移和侵袭,但通过靶向miR-125a和上调MTDH,促进乳腺癌细胞中的凋亡,暗示乳腺癌恶性进展中的新型TP73-AS1 / miR-125A / MTDH途径。 2019年的作者。中国肺部肿瘤集团和约翰瓦里和儿子澳大利亚发表的胸癌

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