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LINC00665 通过靶向 miR-181a-5p/FHDC 促进卵巢癌细胞增殖并抑制细胞凋亡。

LncRNA LINC00665 Promotes Ovarian Cancer Cell Proliferation and Inhibits Apoptosis via Targeting miR-181a-5p/FHDC.

机构信息

Department of Women's Health, Women's Hospital of Nanjing Medical University, Nanjing Maternity and Child Health Care Hospital, Nanjing, 210004, Jiangsu Province, China.

Department of Gynecological Oncology Surgery, Jiangsu Cancer Hospital (Jiangsu Institute of Cancer Research, Nanjing Medical University Affiliated Cancer Hospital), 42 Baiziting Road, Nanjing, 210009, Jiangsu Province, China.

出版信息

Appl Biochem Biotechnol. 2022 Sep;194(9):3819-3832. doi: 10.1007/s12010-022-03943-3. Epub 2022 May 7.

Abstract

Previous reports indicate that long intergenic non-coding RNA LINC00665 naturally occurred vital effects in various cancers. Herein, the role of LINC00665 in ovarian cancer progress was explored. We found that LINC00665 was upregulated in ovarian cancer cell lines. Besides, a series of assays including flow cytometry, wound-healing, transwell, cell counting Kit-8 (CCK-8), and EdU assay confirmed that the knockdown of LINC00665 could reduce the viability, proliferation, and migration of SKOV-3 and OVCAR-3 cells. Accumulating evidence indicates that many lncRNAs can function as endogenous miRNA sponges by competitively binding common miRNAs. In this study, the bioinformatics analysis suggests that LNC00665 specifically binds to miR-181a-5p. LINC00665 downregulated the miR-181a-5p in SKOV-3 and OVCAR-3 cells. The knockdown of miR-181a-5p evidently reverses the inhibitory effect of sh-LINC00662. Besides, FH2 domain containing 1 (FHDC1) has been proved to deed as an effective target of miR-181a-5p. The results reveal the knockdown of LINC00665 facilitates ovarian cancer via development by sponging miR-181a-5p and up-regulating FHDC1 expression. These may contribute to ovarian cancer therapy.

摘要

先前的报告表明,长链非编码 RNA LINC00665 在各种癌症中自然存在重要作用。在此,我们探讨了 LINC00665 在卵巢癌进展中的作用。我们发现 LINC00665 在卵巢癌细胞系中上调。此外,一系列实验,包括流式细胞术、划痕愈合、transwell、细胞计数试剂盒(CCK-8)和 EdU 实验,证实敲低 LINC00665 可以降低 SKOV-3 和 OVCAR-3 细胞的活力、增殖和迁移。越来越多的证据表明,许多 lncRNA 可以通过竞争性结合常见的 miRNA 作为内源性 miRNA 海绵发挥作用。在这项研究中,生物信息学分析表明 LINC00665 特异性结合 miR-181a-5p。LINC00665 在 SKOV-3 和 OVCAR-3 细胞中下调 miR-181a-5p。miR-181a-5p 的敲低明显逆转了 sh-LINC00662 的抑制作用。此外,FH2 结构域包含蛋白 1(FHDC1)已被证明是 miR-181a-5p 的有效靶标。这些结果表明,通过海绵吸附 miR-181a-5p 和上调 FHDC1 表达,敲低 LINC00665 促进了卵巢癌的发生。这些可能有助于卵巢癌的治疗。

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