Evidence map›Paper›PMID 34324029›Full record

ArticleArchives of gynecology and obstetrics2022

Circ_0008673 regulates breast cancer malignancy by miR-153-3p/CFL2 axis.

Li Zhang, Wei Zhang, Zhigang Zuo, Jiying Tang, Ying Song, Fengjun Cao, Xiongjie Yu, Shan Liu, Xiaojun Cai

Abstract read
PubMed Publisher
In one paragraph

Article in Archives of gynecology and obstetrics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 24% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 20 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Li Zhang *Department of Oncology, Renmin Hospital, Hubei University of Medicine, 39 Chaoyang Middle Road, Maojian District, Shiyan, 442000, Hubei, China.
Wei Zhang *Department of Oncology, Renmin Hospital, Hubei University of Medicine, 39 Chaoyang Middle Road, Maojian District, Shiyan, 442000, Hubei, China.
Zhigang ZuoDepartment of Oncology, Renmin Hospital, Hubei University of Medicine, 39 Chaoyang Middle Road, Maojian District, Shiyan, 442000, Hubei, China.
Jiying TangDepartment of Oncology, Renmin Hospital, Hubei University of Medicine, 39 Chaoyang Middle Road, Maojian District, Shiyan, 442000, Hubei, China.
Ying SongDepartment of Oncology, Renmin Hospital, Hubei University of Medicine, 39 Chaoyang Middle Road, Maojian District, Shiyan, 442000, Hubei, China.
Fengjun CaoDepartment of Oncology, Renmin Hospital, Hubei University of Medicine, 39 Chaoyang Middle Road, Maojian District, Shiyan, 442000, Hubei, China.
Xiongjie YuDepartment of Oncology, Renmin Hospital, Hubei University of Medicine, 39 Chaoyang Middle Road, Maojian District, Shiyan, 442000, Hubei, China.
Shan LiuDepartment of Oncology, Renmin Hospital, Hubei University of Medicine, 39 Chaoyang Middle Road, Maojian District, Shiyan, 442000, Hubei, China. uprdbq@163.com.
Xiaojun CaiDepartment of Oncology, Renmin Hospital, Hubei University of Medicine, 39 Chaoyang Middle Road, Maojian District, Shiyan, 442000, Hubei, China. nauqaz@163.com.
Hubei University of Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBreast cancer is an aggressive tumor, which poses a heavy burden to human health. Circular RNAs have been involved in the pathogenesis of breast cancer. This study aims to investigate whether circ_0008673 mediates breast cancer malignant progression by microRNA-153-3p (miR-153-3p)/cofilin 2 (CFL2) pathway.

methodsThe RNA levels of circ_0008673, miR-153-3p and CFL2 were detected by quantitative real-time polymerase chain reaction (qRT-PCR). The protein expression of CFL2, E-cadherin and N-cadherin was determined by western blot analysis. Cell proliferation was demonstrated through cell counting kit-8 and cell colony-formation assays. Cell apoptosis was detected by flow cytometry analysis. Cell migratory and invasive capacities were determined by transwell assay. The associated relationship between miR-153-3p and circ_0008673 or CFL2 was predicted by online databases, and testified by dual-luciferase reporter and RNA immunoprecipitation assays. In vivo assay was employed to demonstrate the effects of circ_0008673 silencing on tumor formation in vivo.

resultsCirc_0008673 and CFL2 expressions were upregulated, while miR-153-3p expression was downregulated in breast cancer tissues and cells compared with adjacent normal breast tissues and cells, respectively. Circ_0008673 overexpression promoted cell proliferation, migration and invasion, and repressed cell apoptosis, while circ_0008673 silencing had opposite effects. Additionally, circ_0008673 served as a sponge of miR-153-3p. And circ_0008673 was proved to regulate breast cancer cell malignancy by sponging miR-153-3p. MiR-153-3p was found to modulate breast cancer cell carcinogenesis via targeting CFL2. Furthermore, circ_0008673 silencing repressed tumor growth in vivo.

conclusionCirc_0008673 promoted breast cancer progression by upregulating CFL2 expression through sponging miR-153-3p. This study provides a theoretical basis for researching circRNA-directed treatment of breast cancer.

Indexed as

Breast NeoplasmsMicroRNAsActin Depolymerizing FactorsCell Line, TumorCofilin 2FemaleHumansRNA, CircularActin Depolymerizing FactorsCFL2 protein, humanCofilin 2MicroRNAsMIRN153 microRNA, humanRNA, CircularBreast cancerCFL2circ_0008673miR-153-3p

Identifiers

PMID34324029
OpenAlexW3185108984

What OpenQuestion holds

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Registered trials

None linked

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.