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miR-301b-3p 通过靶向 HOXA5 促进乳腺癌细胞的发生和发展。

MiR-301b-3p Promotes the Occurrence and Development of Breast Cancer Cells via Targeting HOXA5.

机构信息

Surgery Department, The Third Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, 310005, China.

Department of General Surgery, Zhejiang Quhua Hospital, Quzhou, 324000, China.

出版信息

Crit Rev Eukaryot Gene Expr. 2021;31(3):35-44. doi: 10.1615/CritRevEukaryotGeneExpr.2021038215.

Abstract

It has been reported that microRNA (miRNA) is an important regulator in various cancers. In this study, it was found by analyzing The Cancer Genome Atlas (TCGA) and bioinformatics database that miR-301b-3p was highly expressed in breast cancer tissue, while HOXA5 was significantly lower expressed in breast cancer. In addition, they had targeted binding sites. The potential functions of miR-301b-3p and HOXA5 in breast cancer were further studied through a series of biological experiments. Expression levels of miR-301b-3p and HOXA5 were detected by qRT-PCR and western blot. The targeted binding relationship between them was verified by dual-luciferase assay. Cell proliferative, migratory, and invasive abilities of cells were detected by CCK-8 cell proliferation assay, wound healing assay, and transwell assay. The apoptosis of breast cancer cells was detected by flow cytometry. These assays indicated that overexpressing miR-301-3p could promote the proliferation, migration, and invasion of breast cancer cells, and inhibit cell apoptosis. It was shown that miR-301b-3p targeted and inhibited HOXA5 expression by detection of HOXA5 expression after overexpressing miR-301b-3p and the result of dual-luciferase assay. Overexpressing miR-301b-3p could decrease the inhibitory effect of overexpressing HOXA5 on cancer cell proliferation, migration, and invasion. These results proved that miR-301b-3p may promote breast cancer cell growth by inhibiting HOXA5 expression, which provided a new potential target for the prognostic treatment of breast cancer patients.

摘要

据报道,微小 RNA(miRNA)是各种癌症的重要调节因子。在这项研究中,通过分析癌症基因组图谱(TCGA)和生物信息学数据库发现,miR-301b-3p 在乳腺癌组织中高表达,而 HOXA5 在乳腺癌中表达明显降低。此外,它们具有靶向结合位点。通过一系列生物学实验进一步研究了 miR-301b-3p 和 HOXA5 在乳腺癌中的潜在功能。通过 qRT-PCR 和 Western blot 检测 miR-301b-3p 和 HOXA5 的表达水平。通过双荧光素酶报告基因实验验证它们之间的靶向结合关系。通过 CCK-8 细胞增殖实验、划痕愈合实验和 Transwell 实验检测细胞的增殖、迁移和侵袭能力。通过流式细胞术检测乳腺癌细胞的凋亡。这些实验表明,过表达 miR-301b-3p 可以促进乳腺癌细胞的增殖、迁移和侵袭,并抑制细胞凋亡。通过检测过表达 miR-301b-3p 后 HOXA5 的表达以及双荧光素酶报告基因实验的结果表明,miR-301b-3p 通过靶向抑制 HOXA5 的表达来发挥作用。过表达 miR-301b-3p 可以降低过表达 HOXA5 对癌细胞增殖、迁移和侵袭的抑制作用。这些结果证明,miR-301b-3p 可能通过抑制 HOXA5 的表达促进乳腺癌细胞生长,为乳腺癌患者的预后治疗提供了一个新的潜在靶点。

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