Evidence map›Paper›PMID 26379838›Full record

ArticleInternational journal of clinical and experimental medicine2015

Silencing of DUSP6 gene by RNAi-mediation inhibits proliferation and growth in MDA-MB-231 breast cancer cells: an in vitro study.

Hongming Song, Chenyang Wu, Chuankui Wei, Dengfeng Li, Kaiyao Hua, Jialu Song, Hui Xu, Lei Chen, Lin Fang

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

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  14. A Two-Gene Prognostic Classifier for Early-Stage Lung Squamous Cell Carcinoma in Multiple Large-Scale and Geographically Diverse Cohorts.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2017
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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.

Hongming SongDepartment of General Surgery, Shanghai Tenth People's Hospital, School of Medicine, Tongji University Shanghai 200072, China.
Chenyang WuDepartment of General Surgery, Shanghai Tenth People's Hospital, School of Medicine, Tongji University Shanghai 200072, China.
Chuankui WeiDepartment of General Surgery, Shanghai Tenth People's Hospital, School of Medicine, Tongji University Shanghai 200072, China.
Dengfeng LiDepartment of General Surgery, Shanghai Tenth People's Hospital, School of Medicine, Tongji University Shanghai 200072, China.
Kaiyao HuaDepartment of General Surgery, Shanghai Tenth People's Hospital, School of Medicine, Tongji University Shanghai 200072, China.
Jialu SongDepartment of General Surgery, Shanghai Tenth People's Hospital, School of Medicine, Tongji University Shanghai 200072, China.
Hui XuDepartment of General Surgery, Shanghai Tenth People's Hospital, School of Medicine, Tongji University Shanghai 200072, China.
Lei ChenDepartment of General Surgery, Shanghai Tenth People's Hospital, School of Medicine, Tongji University Shanghai 200072, China.
Lin FangDepartment of General Surgery, Shanghai Tenth People's Hospital, School of Medicine, Tongji University Shanghai 200072, China.
Shanghai Tenth People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDual-specificity phosphatase 6 (DUSP6) is a negative feedback mechanism of the mitogen-activated protein (MAP) kinase superfamily (MAPK/ERK, SAPK/JNK, p38), that is associated with cellular proliferation and differentiation. It has been reported that the expression of DUSP6 in different types of breast cancer is diverse and therefore it has altered functions in various types of breast cancer. Our aim was to explore the exact function of DUSP6 in triple-negative breast cancer cells (MDA-MB-231 cell) and to determine whether the suppression of DUSP6 by small interfering RNA (siRNA) and mircroRNA (miRNA) inhibits the growth of human MDA-MB-231 breast cancer cells.

methodsDUSP6-siRNA was used to inhibit the expression of DUSP6 directly and miR-145 to inhibit the expression of DUSP6 either in MDA-MB-231 breast cancer cells and successful transfection being confirmed by Real-time PCR and Western Blotting. Down regulation of DUSP6 in MDA-MB-231 cells suppressed the cell proliferation as investigated by MTT assay and colony form assay. Transwell test and Scratch assay were conducted to investigate the migration and invasion of MDA-MB-231 cells. T-test (two-tailed) was used to compare differences between groups, and the significance level was set at P<0.05.

resultsDUSP6 mRNA expression and protein expression were reduced after transfection with DUSP6-siRNA directly and similar trend with transfection with miR-145. The treated group with DUSP6-siRNA or miR-145 suppressed MDA-MB-231 cells proliferation, migration and invasion, and meanwhile the cells were arrested at G0/G1 phase.

conclusionsDUSP6 plays a role in triple-negative breast cancer cells that might promote growth in MDA-MB-231 triple-negative breast cancer cells.

Indexed as

breast cancerDUSP6MDA-MB-231 cellsmiR-145siRNA

Identifiers

PMID26379838
PMCPMC4565221
OpenAlexW2412004310

What OpenQuestion holds

Textmetadata
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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.