Evidence map›Paper›PMID 28393251›Full record

ArticleOncology reports2017

miR-597 inhibits breast cancer cell proliferation, migration and invasion through FOSL2.

Jiangtu He, Jieying Mai, Yan Li, Linyi Chen, Hui Xu, Xiaofei Zhu, Qiuhui Pan

Open access · hybridAbstract read
In one paragraph

Article in Oncology reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

26 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Progress in the Study of Fra-2 in Respiratory Diseases.International journal of molecular sciences · 2024
    Review
  3. Article
  4. Role of Fra-2 in cancer.Cell death and differentiation · 2024
    Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Identification of Acute Myeloid Leukemia Bone Marrow Circulating MicroRNAs.International journal of molecular sciences · 2020
    Article
  20. Article
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 4 institutions in 1 country.

Jiangtu HeThe Research Center for Immunology, School of Laboratory Medicine, Xinxiang Medical University, Xinxiang, Henan 453003, P.R. China.
Jieying MaiDepartment of Central Laboratory, Tenth People's Hospital of Tongji University, Shanghai 200072, P.R. China.
Yan LiDepartment of Clinical Laboratory, Maternal and Child Health Care of Zaozhuang, Zaozhuang, Shandong 277102, P.R. China.
Linyi ChenDepartment of Ophthalmology, Tai Zhou Hospital of Zhejiang Province, Taizhou, Zhejiang 317099, P.R China.
Hui XuDepartment of Ophthalmology, Tai Zhou Hospital of Zhejiang Province, Taizhou, Zhejiang 317099, P.R China.
Xiaofei ZhuThe Research Center for Immunology, School of Laboratory Medicine, Xinxiang Medical University, Xinxiang, Henan 453003, P.R. China.
Qiuhui PanDepartment of Central Laboratory, Tenth People's Hospital of Tongji University, Shanghai 200072, P.R. China.
Tongji University · CNXinxiang Medical University · CNZhejiang Taizhou Hospital · CNZaozhuang Municipal Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many reports suggest that the discovery of microRNAs (miRNAs) might provide a novel therapeutical target for many diseases, even of human cancers; however, there are no reports on the role of miR-597 in human cancers. In the present study, by detecting mRNA expression with qRT-PCR, compared with the adjacent normal tissues we found that miR-597 was significantly downregulated in breast cancer tissues. By using the MTT assay, the cell wound-healing assay and the cell invasion assay, we demonstrated that miR-597 mimics were able to suppress breast cancer cell proliferation, migration and invasion. Additionally, with flow cytometry, we found that mir-597 influenced the growth of breast cancer cells through regulating the G1-S phase transition. Furthermore, we identified one binding site for miR-597 at the 3'UTR of the FOSL2 gene, using bioinformatics methods and the luciferase reporter assay, it was confirmed that FOSL2 was a direct target of miR-597. Moreover, overexpression of FOSL2 in MDA-MB‑231 and SK-BR-3 cells can block the vast majority of the miR-597 roles, suggesting that miR-597 acts as a tumor suppressor in breast cancer cells by the downregulation of FOSL2. Additionally, we also found a negative correlation between the expression of FOSL2 and miR-597 in the tumor samples. This new regulatory mechanism in breast cancer may provide another method for diagnosis and therapy.

Indexed as

Breast NeoplasmsCell Line, TumorCell MovementCell ProliferationFemaleFos-Related Antigen-2Gene Expression Regulation, NeoplasticHumansMicroRNAsFOSL2 protein, humanFos-Related Antigen-2MicroRNAsMIRN-598 microRNA, human

Identifiers

PMID28393251
PMCPMC5428280
OpenAlexW2605114885

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.