Evidence map›Paper›PMID 38376577›Full record

ArticleBiochemical genetics2024

Circ-RNF111 Promotes Proliferation of Ovarian Cancer Cell SKOV-3 by Targeting the MiR-556-5p/CCND1 Axis.

Li Zuo, Yue Tan, Qiao-Ling Xu, Xiao-Li Li, Mi Xiao

Abstract read
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Article in Biochemical genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Li Zuo *Department of Oncology, Fudan University Shanghai Cancer Center, Minhang Branch, Shanghai, 200240, China.
Yue Tan *Department of Oncology, Fudan University Shanghai Cancer Center, Minhang Branch, Shanghai, 200240, China.
Qiao-Ling XuDepartment of Oncology, Fudan University Shanghai Cancer Center, Minhang Branch, Shanghai, 200240, China.
Xiao-Li LiDepartment of Oncology, Fudan University Shanghai Cancer Center, Minhang Branch, Shanghai, 200240, China.
Mi XiaoDepartment of Oncology, Fudan University Shanghai Cancer Center, Minhang Branch, Shanghai, 200240, China. fbsci123456@163.com.

Funding

the science and Technology Commission of Minhang District, Shanghai 2022MHZ053
6 · The paper itself

Abstract

The aim of this study was to investigate the role and mechanism of circ-RNF111 in the human ovarian cancer cell line SKOV-3. First, qRT-PCR was used to detect circ-RNF111 and miR-556-5p expression levels in human normal ovarian epithelial cells IOSE80 and human ovarian cancer cells SKOV-3. CCK-8 and colony formation assays were adopted to determine the proliferation rate and cell viability of SKOV-3 cells, respectively. Additionally, in an attempt to reveal the mechanism of circ-RNF111, we predicted the targeting relationship between miR-556-5p and circ-RNF111 as well as miR-556-5p and CCND1 using the circinteractome and TargetScan databases, respectively, and validated their relationship by dual-luciferase reporter assay. The protein expression levels of CCND1 in SKOV-3 cells were detected by Western blot. Based on the above experiments, the expression of circ-RNF111 was found to be up-regulated in SKOV-3, and the knockdown of circ-RNF111 significantly inhibited the proliferation and viability of SKOV-3 cells. Then we confirmed that circ-RNF111 sponged miR-556-5p in SKOV-3 cells to up-regulate CCND1 expression. In addition, simultaneous inhibition of miR-556-5p or overexpression of CCND1 in SKOV-3 cells with knockdown of circ-RNF111 reversed the inhibitory effect of knockdown of circ-RNF111 on the protein expression level of CCND1, cell proliferation rate, and cell viability. In summary, circ-RNF111 promotes the proliferation of SKOV-3 cells by targeting the miR-556-5p/CCND1 axis. Circ-RNF111 may serve as a potential target for ovarian cancer therapy.

Indexed as

Cell ProliferationCyclin D1MicroRNAsOvarian NeoplasmsRNA, CircularCell Line, TumorFemaleGene Expression Regulation, NeoplasticHumansCCND1 protein, humanCyclin D1MicroRNAsMIRN576 microRNA, humanRNA, CircularCCND1Circ-RNF111MiR-556-5pOvarian cancer

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.