Evidence map›Paper›PMID 28560951›Full record

ArticleOncology research2018

miR-3188 Regulates Cell Proliferation, Apoptosis, and Migration in Breast Cancer by Targeting TUSC5 and Regulating the p38 MAPK Signaling Pathway.

Xiaowen Chen, Jianli Chen

RetractedOpen access · hybridAbstract readRetracted Publication
In one paragraph

Article in Oncology research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 25% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
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  3. Review
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  9. Review
  10. Article
  11. Loss of exosomal miR-3188 in cancer-associated fibroblasts contributes to HNC progression.Journal of experimental & clinical cancer research : CR · 2019
    Article
  12. MicroRNAs in Female Malignancies.Cancer informatics · 2019
    Article
  13. Article
  14. Article
  15. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 1 country.

Xiaowen ChenDepartment of Oncology Center, Affiliated Hospital of Guangdong Medical CollegeZhanjiang, GuangdongP.R. China.
Jianli ChenThe Third Department of Medical Oncology, The Third Affiliated Hospital of Xinxiang Medical UniversityXinxiang, HenanP.R. China.
Guangdong Medical College · CNXinxiang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study intended to investigate the effects of miR-3188 on breast cancer and to reveal the possible molecular mechanisms. miR-3188 was upregulated and TUSC5 was downregulated in breast cancer tissues and MCF-7 cells compared to normal tissue and MCF-10 cells. After MCF-7 cells were transfected with miR-3188 inhibitor, cell proliferation and migration were inhibited, whereas apoptosis was promoted. Luciferase reporter assay suggested that TUSC5 was a target gene of miR-3188. In addition, miR-3188 overexpression increased the p-p38 expression, while miR-3188 suppression decreased the p-p38 expression significantly. miR-3188 regulated breast cancer progression via the p38 MAPK signaling pathway. In conclusion, miR-3188 affects breast cancer cell proliferation, apoptosis, and migration by targeting TUSC5 and activating the p38 MAPK signaling pathway. miR-3188 may serve as a potential therapeutic agent for the treatment of breast cancer.

Indexed as

ApoptosisCell MovementCell ProliferationBiomarkers, TumorBreast NeoplasmsCase-Control StudiesFemaleGene Expression Regulation, NeoplasticHumansMembrane ProteinsMicroRNAsp38 Mitogen-Activated Protein KinasesPrognosisTumor Cells, CulturedTumor Suppressor ProteinsBiomarkers, TumorMembrane ProteinsMicroRNAsMIRN3188 microRNA, humanp38 Mitogen-Activated Protein KinasesTRARG1 protein, humanTumor Suppressor Proteins

Identifiers

PMID28560951
PMCPMC7844837
OpenAlexW2619716020

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.