长链非编码RNA LINC00473通过miR-424-5p/CCNE1途径促进乳腺癌进展

IF 1 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Protein and Peptide Letters Pub Date : 2023-01-01 DOI:10.2174/0929866530666221026164454
Chao Zhang, Ting Yang
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引用次数: 2

摘要

背景:女性乳腺癌(BC)的发病率有很大的增加。LINC00473是一种与癌症相关的lncRNA,参与了许多癌症的进展,但其在BC进展中的作用有待进一步阐述。方法:采用实时定量聚合酶链反应(qRT-PCR)技术,定量检测BC组织和细胞中LINC00473、miR-424-5p、cyclin E1 (CCNE1) mRNA的表达水平。采用细胞计数试剂盒-8 (CCK-8)法检测细胞活力;采用Transwell法评价细胞迁移和侵袭能力。采用Western blot和免疫组化(IHC)技术研究CCNE1蛋白的表达;采用双荧光素酶报告基因测定来阐明LINC00473、miR-424-5p和CCNE1之间的靶向关系。结果:LINC00473在BC组织细胞系中表达升高,与BC患者淋巴结转移及临床分期升高有关。LINC00473被证明是miR-424-5p的分子海绵;LINC00473敲低抑制了BC细胞的生长、迁移、侵袭和上皮-间质转化,而miR-424-5p抑制剂可以消除这些影响;miR-424-5p靶向CCNE1抑制其表达。LINC00473正向调节CCNE1的表达,CCNE1的恢复抵消了LINC00473敲低对BC细胞的影响。结论:LINC00473通过miR-424-5p/CCNE1轴促进BC的进展。
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Long Non-coding RNA LINC00473 Promotes Breast Cancer Progression via miR-424-5p/CCNE1 Pathway.

Background: There has been a large increase in the incidence of breast cancer (BC) among women. LINC00473 is a cancer-related lncRNA, participating in the progression of many cancers, but its role in the progression of BC awaits more elaboration.

Methods: Quantitative real-time polymerase chain reaction (qRT-PCR) was used to quantify LINC00473, miR-424-5p, and cyclin E1 (CCNE1) mRNA expression levels in BC tissues and cells. Cell counting kit-8 (CCK-8) assay was employed to detect the cell viability; the cell migration and invasion abilities were evaluated by the Transwell assay. Western blot and immunohistochemistry (IHC) were adopted to study CCNE1 protein expression; dual-luciferase reporter assay was performed to clarify the targeting relationships among LINC00473, miR-424-5p, and CCNE1.

Results: LINC00473 expression was elevated in BC tissues and cell lines, which was associated with lymph node metastasis and higher clinical stage of the patients with BC. LINC00473 proved to be a molecular sponge for miR-424-5p; LINC00473 knockdown impeded the growth, migration, invasion, and epithelial-mesenchymal transition of BC cells, while these effects were abolished by miR-424-5p inhibitors; miR-424-5p targeted CCNE1 to restrain its expression. LINC00473 positively regulated CCNE1 expression, and CCNE1 restoration counteracted the effects induced by LINC00473 knockdown in BC cells.

Conclusion: LINC00473 facilitates the progression of BC through miR-424-5p/CCNE1 axis.

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来源期刊
Protein and Peptide Letters
Protein and Peptide Letters 生物-生化与分子生物学
CiteScore
2.90
自引率
0.00%
发文量
98
审稿时长
2 months
期刊介绍: Protein & Peptide Letters publishes letters, original research papers, mini-reviews and guest edited issues in all important aspects of protein and peptide research, including structural studies, advances in recombinant expression, function, synthesis, enzymology, immunology, molecular modeling, and drug design. Manuscripts must have a significant element of novelty, timeliness and urgency that merit rapid publication. Reports of crystallization and preliminary structure determination of biologically important proteins are considered only if they include significant new approaches or deal with proteins of immediate importance, and preliminary structure determinations of biologically important proteins. Purely theoretical/review papers should provide new insight into the principles of protein/peptide structure and function. Manuscripts describing computational work should include some experimental data to provide confirmation of the results of calculations. Protein & Peptide Letters focuses on: Structure Studies Advances in Recombinant Expression Drug Design Chemical Synthesis Function Pharmacology Enzymology Conformational Analysis Immunology Biotechnology Protein Engineering Protein Folding Sequencing Molecular Recognition Purification and Analysis
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