Evidence map›Paper›PMID 26221232›Full record

ArticleInternational journal of clinical and experimental medicine2015

MiR-300 regulate the malignancy of breast cancer by targeting p53.

Xiao-Heng Xu, Da-Wei Li, Hui Feng, Hong-Mei Chen, Yan-Qiu Song

RetractedOpen 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. It has been retracted, and should not be counted. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

17 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. miRNA-driven sensitization of breast cancer cells to Doxorubicin treatment following exposure to low dose of Zinc Oxide nanoparticles.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2024
    Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Bioinformatics Analysis Identifies MicroRNAs and Target Genes Associated with Prognosis in Patients with Melanoma.Medical science monitor : international medical journal of experimental and clinical research · 2019
    Article
  10. Article
  11. Article
  12. Regulation of epithelial-mesenchymal transition through microRNAs: clinical and biological significance of microRNAs in breast cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Review
  13. Article
  14. Article
  15. microRNA regulators of apoptosis in cancer.Discoveries (Craiova, Romania) · 2016
    Review
  16. Article
  17. Article
4 · The record

Corrections and comments

  • Retraction · 2025-03-01Falsification/Fabrication of Data · Investigation by Journal/Publisher · Investigation by Third Party ·
5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Xiao-Heng XuCancer Center, The First Hospital of Jilin University, Changchun Jilin P. R. China.
Da-Wei LiDepartment of Neurology, Affiliated Hospital of Beihua University Jilin, P. R. China.
Hui FengCancer Center, The First Hospital of Jilin University, Changchun Jilin P. R. China.
Hong-Mei ChenCancer Center, The First Hospital of Jilin University, Changchun Jilin P. R. China.
Yan-Qiu SongCancer Center, The First Hospital of Jilin University, Changchun Jilin P. R. China.
Jilin University · CNBeihua University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveIn this study, we investigated the role of miR-300 in regulating cell proliferation and invasion of breast cancer (BC) cells.

methodsMicroRNA and protein expression patterns were compared between breast cancer tissue and normal tissue and between two different prognostic groups. The up-regulation of miR-300 was confirmed by real-time reverse transcription polymerase chain reaction and its expression was analyzed in MCF-7 breast cancer cells.

resultsWe observed that miR-300 expression was frequently and dramatically up-regulated in human breast cancer tissues and cell lines compared with the matched adjacent normal tissues and cells. We further showed that transient and stable over-expression of miR-300 could promote cell proliferation and cell cycle progression. Moreover, p53, a key inhibitor of cell cycle, was verified as a direct target of miR-300, suggesting that miR-300 might promote breast cancer cell proliferation and invasion by regulating p53 expression.

conclusionOur findings indicated that miR-300 up-regulation might exert some sort of antagonistic function by targeting p53 in breast cancer cell proliferation during breast tumorigenesis.

Indexed as

breast cancerMCF-7MiR-300p53target therapy

Identifiers

PMID26221232
PMCPMC4509177
OpenAlexW985461568

What OpenQuestion holds

Textmetadata
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.