Evidence map›Paper›PMID 33061615›Full record

ArticleCancer management and research2020

Long Non-Coding RNA H19 Promotes Proliferation, Migration and Invasion and Inhibits Apoptosis of Breast Cancer Cells by Targeting miR-491-5p/ZNF703 Axis.

Yongkun Wang, Zhen Wu, Yingxue Li, Zheng Zheng, Jinqiang Yan, Shuyan Tian, Lin Han

Open access · goldAbstract read
In one paragraph

Article in Cancer management and research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
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  9. LncRNA H19: A novel oncogene in multiple cancers.International journal of biological sciences · 2021
    Review
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 2 institutions in 1 country.

Yongkun Wang *Department of Thyroid Surgery, Liaocheng People's Hospital (Clinical Hospital of Shandong First Medical University) Liaocheng, Shandong, People's Republic of China.
Zhen Wu *Department of Thyroid Surgery, Liaocheng People's Hospital (Clinical Hospital of Shandong First Medical University) Liaocheng, Shandong, People's Republic of China.
Yingxue LiDepartment of Pathology, Liaocheng People's Hospital (Clinical Hospital of Shandong First Medical University) Liaocheng, Shandong, People's Republic of China.
Zheng ZhengDepartment of Pathology, Liaocheng People's Hospital (Clinical Hospital of Shandong First Medical University) Liaocheng, Shandong, People's Republic of China.
Jinqiang YanDepartment of Pathology, Liaocheng People's Hospital (Clinical Hospital of Shandong First Medical University) Liaocheng, Shandong, People's Republic of China.
Shuyan TianDepartment of Pathology, Liaocheng People's Hospital (Clinical Hospital of Shandong First Medical University) Liaocheng, Shandong, People's Republic of China.
Lin HanDepartment of Pathology, Liaocheng People's Hospital (Clinical Hospital of Shandong First Medical University) Liaocheng, Shandong, People's Republic of China.
Liaocheng People's Hospital · CNShandong First Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBreast cancer is one of the most common cancers worldwide. Long non-coding RNAs and microRNAs act as important regulators in human cancers. This study aims to explore the molecular mechanism among H19, miR-491-5p and zinc finger 703 (ZNF703) in breast cancer. MATERIALS AND

methodsQuantitative real-time polymerase chain reaction (qRT-PCR) was conducted to detect the expression of H19, miR-491-5p and ZNF703. Cell Counting Kit 8 (CCK-8) assay was performed to evaluate cell proliferation. Cell apoptosis was assessed by flow cytometry assay. The number of migrated and invaded cells was counted by transwell assay. Dual luciferase reporter assay was carried out to test luciferase activity. Protein level of ZNF703 was measured by Western blot assay.

resultsH19 was highly expressed in breast tissues and cells. H19 knockdown inhibited proliferation, induced apoptosis and blocked migration and invasion. Moreover, H19 bound to miR-491-5p and negatively regulated miR-491-5p expression. MiR-491-5p inhibition abrogated the activities of proliferation, apoptosis, migration and invasion affected by H19 knockdown. Furthermore, miR-491-5p directly targeted ZNF703 and inversely modulated ZNF703 expression. ZNF703 up-regulation rescued the effects of miR-491-5p overexpression on proliferation, apoptosis, migration and invasion. In addition, H19 knockdown reduced ZNF703 expression by targeting miR-491-5p/ZNF703 axis.

conclusionH19 promoted proliferation, migration and invasion and retarded apoptosis of breast cancer cells via sponging miR-491-5p to down-regulate ZNF703 expression.

Indexed as

breast cancerH19miR-491-5pZNF703

Identifiers

PMID33061615
PMCPMC7532042
OpenAlexW3088680939

What OpenQuestion holds

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LicenceCC BY-NC
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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.