Evidence map›Paper›PMID 32256819›Full record

ArticleOncology letters2020

miR-320/ELF3 axis inhibits the progression of breast cancer via the PI3K/AKT pathway.

Zhiqiang Zhang, Jinku Zhang, Jinmei Li, Huijuan Geng, Bingjuan Zhou, Bingxin Zhang, Hong Chen

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

22 citing papers in PubMed, 33 citations in OpenAlex.

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  20. Regulation of MethylaseDiabetes, metabolic syndrome and obesity : targets and therapy · 2021
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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.

Zhiqiang ZhangDepartment of Thoracic Surgery, Baoding First Central Hospital, Baoding, Hebei 071000, P.R. China.
Jinku ZhangDepartment of Pathology, Baoding First Central Hospital, Baoding, Hebei 071000, P.R. China.
Jinmei LiDepartment of Pathology, Baoding First Central Hospital, Baoding, Hebei 071000, P.R. China.
Huijuan GengDepartment of Clinical Laboratory, Baoding Infectious Diseases Hospital, Baoding, Hebei 071000, P.R. China.
Bingjuan ZhouDepartment of Pathology, Baoding First Central Hospital, Baoding, Hebei 071000, P.R. China.
Bingxin ZhangDepartment of Pathology, Baoding First Central Hospital, Baoding, Hebei 071000, P.R. China.
Hong ChenDepartment of Pathology, Baoding First Central Hospital, Baoding, Hebei 071000, P.R. China.
Baoding People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is increasing evidence demonstrating that disorders affecting microRNAs (miRs) influence tumorigenesis and progression, which results in a poor prognosis in patients with breast cancer (BC). In the present study, the precise molecular mechanism underlying the role of miR-320 in the progression of BC was investigated. Reverse transcription-quantitative PCR was conducted to determine mRNA expression, and western blot analysis was used to test protein levels. An MTT assay was conducted to detect cell viability and Transwell assays were used to analyze cell migration and invasion abilities. Furthermore, E74-like factor 3 (ELF3) protein density was tested via immunohistochemistry. Tumor volume was detected by xenograft tumor formation assay. The current results indicated that miR-320 expression was downregulated in BC tissues and cells, and was associated with a poor prognosis of patients with BC. Overexpression of miR-320 inhibited cell proliferation, migration and invasion via inhibition of the epithelial-mesenchymal transition and the PI3K/AKT signaling pathway in BC cells. Furthermore, it was revealed that the tumor size and weight were smaller in nude mice that had been transfected to overexpress miR-320. The luciferase reporter assay demonstrated the direct binding of miR-320 to the 3' untranslated region of ELF3 mRNA, which may further downregulate ELF3. Overall, the present results provided evidence that miR-320 may be a tumor suppressor in BC, and that the miR-320/ELF3 axis regulated tumor progression via the PI3K/AKT signaling pathway, which may represent a novel treatment strategy for BC.

Indexed as

breast cancerE74-like factor 3microRNA-320PI3K/AKT

Identifiers

PMID32256819
PMCPMC7074334
OpenAlexW3010469865

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.