Evidence map›Paper›PMID 33488122›Full record

ArticleCancer management and research2021

MiR-491-5p, as a Tumor Suppressor, Prevents Migration and Invasion of Breast Cancer by Targeting ZNF-703 to Regulate AKT/mTOR Pathway.

Jingyun Guo, Can Luo, Yuqin Yang, Jianyu Dong, Zhaoze Guo, Jinlamao Yang, Huining Lian, Changsheng Ye, Minfeng Liu

Open access · goldAbstract read
In one paragraph

Article in Cancer management and research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

20 citing papers in PubMed, 26 citations in OpenAlex.

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  13. Differentially expressed mRNAs and their upstream miR-491-5p in patients with coronary atherosclerosis as well as the function of miR-491-5p in vascular smooth muscle cells.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2022
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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.

Jingyun Guo *Breast Center, Department of General Surgery, Nanfang Hospital, Southern Medical University, Guangzhou 510515, People's Republic of China.
Can Luo *Breast Center, Department of General Surgery, Nanfang Hospital, Southern Medical University, Guangzhou 510515, People's Republic of China.
Yuqin Yang *Breast Center, Department of General Surgery, Nanfang Hospital, Southern Medical University, Guangzhou 510515, People's Republic of China.ORCID 0000-0002-5086-8858
Jianyu DongBreast Center, Department of General Surgery, Nanfang Hospital, Southern Medical University, Guangzhou 510515, People's Republic of China.
Zhaoze GuoBreast Center, Department of General Surgery, Nanfang Hospital, Southern Medical University, Guangzhou 510515, People's Republic of China.
Jinlamao YangBreast Center, Department of General Surgery, Nanfang Hospital, Southern Medical University, Guangzhou 510515, People's Republic of China.
Huining LianBreast Center, Department of General Surgery, Nanfang Hospital, Southern Medical University, Guangzhou 510515, People's Republic of China.
Changsheng YeBreast Center, Department of General Surgery, Nanfang Hospital, Southern Medical University, Guangzhou 510515, People's Republic of China.
Minfeng LiuBreast Center, Department of General Surgery, Nanfang Hospital, Southern Medical University, Guangzhou 510515, People's Republic of China.
Nanfang Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLarge amounts of microRNAs (miRNAs) have been reported to be aberrantly expressed in malignant cancers. MiR-491-5p makes a significant contribution to the inhibition of multiple cancer processes. However, the specific mechanism and function of miR-491-5p and in breast cancer (BC) is still not fully elucidated.

methodsMiR-491-5p and ZNF-703 expressions or gene transfection effects were identified by RT-qPCR or Western blot in BC tissues or cells. And ZNF-703 expression was monitored through immunohistochemistry method. Cellular function was also confirmed using Transwell assay. Besides, AKT/mTOR pathway-related proteins were analyzed using Western blotting analysis. Moreover, the interplay between miR-491-5p and ZNF-703 was verified through dual-luciferase reporter assay.

resultsmiR-491-5p was lowly expressed, ZNF-703 was highly expressed in BC, and miR-491-5p with low expression and ZNF-703 with high expression were associated with poor prognosis of BC patients. Results of cellular function revealed that overexpression of miR-491-5p markedly suppressed BC cell migration and invasion, and knockdown of miR-491-5p had the opposite effect. Besides, mechanism research disclosed that miR-491-5p directly could bind to ZNF-703 and downregulate ZNF-703. Moreover, we proved that ZNF-703 could prominently reverse the influences of miR-491-5p on the migration and invasion of BC cells. More importantly, the data revealed that miR-491-5p repressed AKT/mTOR pathway by ZNF-703 in BC cells.

conclusionMiR-491-5p prominently suppresses the metastasis of BC cells through ZNF-703 to regulate AKT/mTOR pathway, indicating that miR-491-5p and ZNF-703 might be served as the potential therapeutic targets for BC.

Indexed as

AKT/mTOR pathwaybreast cancermigration and invasionmiR-491-5pZNF-703

Identifiers

PMID33488122
PMCPMC7816048
OpenAlexW3119061015

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.