Evidence map›Paper›PMID 32469064›Full record

ArticleBioscience reports2020

NR2F2-AS1 accelerates cell proliferation through regulating miR-4429/MBD1 axis in cervical cancer.

Dan Liu, Kejin Huang, Tiaojiao Wang, Xufeng Zhang, Wentao Liu, Xiaolong Yue, Jin Wu

Open access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

13 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

7 authors at 1 institution in 1 country.

Dan Liu *The Seventh Department of the Internal Medicine, Harbin Medical University Cancer Hospital, Harbin 150081, Heilongjiang, China.
Kejin Huang *Department of Gynecology, Harbin Medical University Cancer Hospital, Harbin 150081, Heilongjiang, China.
Tiaojiao WangThe Seventh Department of the Internal Medicine, Harbin Medical University Cancer Hospital, Harbin 150081, Heilongjiang, China.
Xufeng ZhangThe Seventh Department of the Internal Medicine, Harbin Medical University Cancer Hospital, Harbin 150081, Heilongjiang, China.
Wentao LiuThe Seventh Department of the Internal Medicine, Harbin Medical University Cancer Hospital, Harbin 150081, Heilongjiang, China.
Xiaolong YueThe Seventh Department of the Internal Medicine, Harbin Medical University Cancer Hospital, Harbin 150081, Heilongjiang, China.
Jin WuThe Seventh Department of the Internal Medicine, Harbin Medical University Cancer Hospital, Harbin 150081, Heilongjiang, China.
Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cervical cancer is one of the most frequent malignant tumors in female. Increasing studies have demonstrated that long noncoding RNAs (lncRNAs) play a key role in the development of multiple cancers. Although some studies have confirmed that lncRNA NR2F2 antisense RNA 1 (NR2F2-AS1) is a pro-cancer gene in many cancers, the molecular mechanism of NR2F2-AS1 in cervical cancer has not been completely elucidated. In the present study, our results revealed that NR2F2-AS1 expression was up-regulated in cervical cancer tissues and cells, notably in patients with advanced cervical cancer. NR2F2-AS1 accelerated progression of cervical cancer by facilitating cell proliferation, migration, invasion, and EMT process, but inhibiting cell apoptosis. Moreover, NR2F2-AS1 acted as a molecular sponge of miR-4429 and methyl-CpG-binding domain protein 1 (MBD1) was a downstream target of miR-4429 in cervical cancer. Furthermore, there was a negative correlation between miR-4429 expression and NR2F2-AS1 or MBD1 expression in tumor tissues. Rescue experiments confirmed that MBD1 overexpression partly rescued NR2F2-AS1 knockdown-mediated inhibition of progression in cervical cancer. To sum up, these results suggested the potential mechanism of NR2F2-AS1 in cervical cancer and revealed that NR2F2-AS1 exerted its carcinogenic effect via regulating miR-4429/MBD1 axis, indicating a promising insight into the therapeutic target of cervical cancer.

Indexed as

Cell ProliferationApoptosisCell MovementDisease ProgressionDNA-Binding ProteinsEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticHeLa CellsHumansMicroRNAsNeoplasm InvasivenessRNA, Long NoncodingSignal TransductionTranscription FactorsUterine Cervical NeoplasmsDNA-Binding ProteinsMBD1 protein, humanMicroRNAsMIRN4429 microRNA, humanRNA, Long NoncodingTranscription Factorscervical cancerMBD1miR-4429NR2F2-AS1

Identifiers

PMID32469064
PMCPMC7295628
OpenAlexW3030871667

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Registered trials

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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.