Evidence map›Paper›PMID 31688991›Full record

ArticleThe Kaohsiung journal of medical sciences2020

MicroRNA-425-5p promotes breast cancer cell growth by inducing PI3K/AKT signaling.

Li-Feng Zhang, Ji-Gang Zhang, Hao Zhou, Tian-Tian Dai, Feng-Bao Guo, Shao-Yong Xu, Yan Chen

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in The Kaohsiung journal of medical sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04720508 (Aberrant Expression of Circulating Micro RNA as a Biomarker for Diagnosis of Breast Cancer in Egyptian Females), which is not on this map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-weighted citation impact, top 17% 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.

NCT04720508 unknown statusnot on this mapstarted 2021, after this paper: background citation

Aberrant Expression of Circulating Micro RNA as a Biomarker for Diagnosis of Breast Cancer in Egyptian Females

TypeobservationalSponsorAssiut UniversityRan2021 to 2023Enrolled50ConditionsBreast CancerArmsblood sample collection.
3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. 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 2 institutions in 1 country.

Li-Feng ZhangDepartment of General Surgery, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Ji-Gang ZhangDepartment of Emergency Surgery, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Hao ZhouDepartment of General Surgery, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Tian-Tian DaiDepartment of General Surgery, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Feng-Bao GuoDepartment of Emergency Surgery, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Shao-Yong XuDepartment of General Surgery, People's Hospital of Shiqian County, Tongren, Guizhou, China.
Yan ChenDepartment of General Surgery, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.ORCID https://orcid.org/0000-0001-7966-8406
Soochow University · CNTongren Hospital · CN

Funding

Natural Science Foundation for colleges and universities in Jiangsu Province 17KJB320013
6 · The paper itself

Abstract

MicroRNA-425-5p (miR-425-5p) has been reported to be involved in the tumorigenesis of several tumors, but its function in breast cancer is still unknown. In this study, miR-425-5p was found significantly upregulated in breast cancer cells, and predicted a poor prognosis for breast cancer patients. Overexpression of miR-425-5p could significantly promote breast cancer cell growth. Further studies showed that overexpression of miR-425-5p upregulated the protein levels of Cyclin D1, Cyclin D3, CDK4, and CDK6. However, inhibiting miR-425-5p downregulated their expression and induced cell cycle arrest at G0/G1 phase. In mechanism, overexpression of miR-425-5p increased the phosphorylation of PI3K p85 and AKT, but inhibiting miR-425-5p displayed opposite effects. Moreover, miR-425-5p bound to the 3'UTR of PTEN mRNA, and downregulated the expression levels of PTEN in both mRNA and protein levels in breast cancer cells. Collectively, the results above demonstrated that miR-425-5p was involved in the tumorigenesis of breast cancer by inducing PI3K/AKT signaling and indicated that miR-425-5p could be as a potential target for breast cancer therapy in the future.

Indexed as

Signal Transduction3' Untranslated RegionsBase SequenceBreast NeoplasmsCell CycleCell Line, TumorCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansMicroRNAsModels, BiologicalPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseUp-Regulation3' Untranslated RegionsMicroRNAsMIRN425 microRNA, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktPTEN PhosphohydrolasePTEN protein, humanAKTbreast cancermicroRNA-425-5pPI3KPTEN

Identifiers

PMID31688991
PMCPMC11896251
OpenAlexW2984009594

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.