Evidence map›Paper›PMID 28038450›Full record

ArticleOncotarget2017

MicroRNA-455-3p promotes invasion and migration in triple negative breast cancer by targeting tumor suppressor EI24.

Zhishuang Li, Qingyong Meng, Aifeng Pan, Xiaojuan Wu, Jingjing Cui, Yan Wang, Li Li

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

53 citing papers in PubMed, 134 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 3 institutions in 1 country.

Zhishuang LiDepartment of Pathology, Shandong University, School of Medicine, Jinan, Shandong, 250012, P.R. China.
Qingyong MengThe No. 2 People's Hospital of Jinan, Jinan, Shandong, 250001, P.R. China.
Aifeng PanDepartment of Pathology, Shandong University, School of Medicine, Jinan, Shandong, 250012, P.R. China.
Xiaojuan WuDepartment of Pathology, Shandong University, School of Medicine, Jinan, Shandong, 250012, P.R. China.
Jingjing CuiDepartment of Thoracic Surgery, Shandong University, Qilu Hospital, Jinan, Shandong, 250012, P.R. China.
Yan WangDepartment of Pathology, Shandong University, School of Medicine, Jinan, Shandong, 250012, P.R. China.
Li LiDepartment of Pathology, Shandong University, School of Medicine, Jinan, Shandong, 250012, P.R. China.
Shandong University · CNFourth People’s Hospital of Jinan · CNQilu Hospital of Shandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lacking of treatment methods for the patients with triple negative breast cancer (TNBC) underscores the pivotal needs to further understand its biology as well as to find better biomarkers and develop novel therapeutic strategies. Increasing evidences support that aberrantly expressed microRNAs (miRNAs) are involved in tumorigenesis and may serve as biomarkers for diagnostic and prognostic purposes of various cancers. In current study, we found that miR-455-3p and miR-196a-5p were intensively overexpressed in TNBC compared with the hormone receptor (HR) positive breast cancer whereas miR-425-5p was down-regulated by miRNA microarray analysis. qRT-PCR analysis confirmed that the expression of miR-455-3p in TNBC cell lines MDA-MB-231 and MDA-MB-468 was higher than that in HR positive breast cancer cell line MCF-7(p<0.01). Functional experiments in vitro showed that miR-455-3p enhanced cell proliferative, invasive and migrational abilities in TNBC cell lines. miRNA targets prediction showed SMAD2, LTBR and etoposide induced 2.4 (EI24) were potential target genes of miR-455-3p, and then it was confirmed by qRT-PCR assay. Dual luciferase reporter assay showed the specific binding of miR-455-3p to 3' UTR of EI24 in TNBC. Then we found miR-455-3p inhibited the EI24 expression at the levels of mRNA and protein. Through small interfering RNA (siRNA) targeting EI24 gene, there were strengthened capabilities of invasion and migration of TNBC cells, and increased expression of EI24 had the inverse effects. In conclusion, the data suggest that miRNA455-3p promotes invasion and migration by targeting tumor suppressor EI24 and might be a potential prognostic biomarker and therapeutic target in TNBC.

Indexed as

Cell MovementGene Expression Regulation, Neoplastic3' Untranslated RegionsApoptosisApoptosis Regulatory ProteinsBiomarkers, TumorCarcinoma, Ductal, BreastCell ProliferationFemaleHumansMicroRNAsNeoplasm InvasivenessNeoplasm StagingNuclear ProteinsPrognosisTriple Negative Breast Neoplasms3' Untranslated RegionsApoptosis Regulatory ProteinsBiomarkers, TumorEI24 protein, humanMicroRNAsMIRN455 microRNA, humanNuclear ProteinsEI24invasionmigrationmiR455-3ptriple negative breast cancer

Identifiers

PMID28038450
PMCPMC5386697
OpenAlexW2564579159

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.