Evidence map›Paper›PMID 31281725›Full record

ArticleJournal of breast cancer2019

miR-148b-3p, miR-190b, and miR-429 Regulate Cell Progression and Act as Potential Biomarkers for Breast Cancer.

Wenzhu Dai, Jixiang He, Ling Zheng, Mingyu Bi, Fei Hu, Minju Chen, Heng Niu, Jingyu Yang, Ying Luo, Wenru Tang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of breast cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

33 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
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  5. Chemopreventive and therapeutic effects ofFrontiers in pharmacology · 2025
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. MicroRNA-190b Targets RFWD3 in Estrogen Receptor-Positive Breast Cancer.Breast cancer : basic and clinical research · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
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  19. Review
  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

11 authors at 2 institutions in 1 country.

Wenzhu DaiLaboratory of Molecular Genetics of Aging & Tumor, Medical School, Kunming University of Science and Technology, Yunnan, China.ORCID 0000-0001-7953-4969
Jixiang HeLaboratory of Molecular Genetics of Aging & Tumor, Medical School, Kunming University of Science and Technology, Yunnan, China.ORCID 0000-0002-6747-2665
Ling ZhengLaboratory of Molecular Genetics of Aging & Tumor, Medical School, Kunming University of Science and Technology, Yunnan, China.ORCID 0000-0002-5432-1569
Mingyu BiLaboratory of Molecular Genetics of Aging & Tumor, Medical School, Kunming University of Science and Technology, Yunnan, China.ORCID 0000-0002-4231-2091
Fei HuLaboratory of Molecular Genetics of Aging & Tumor, Medical School, Kunming University of Science and Technology, Yunnan, China.ORCID 0000-0002-5761-8691
Minju ChenDepartment of Mammary Gland and Thyroid Disease, First People's Hospital of Yunnan Province, Yunnan, China.ORCID 0000-0002-8835-1977
Heng NiuDepartment of Mammary Gland and Thyroid Disease, First People's Hospital of Yunnan Province, Yunnan, China.ORCID 0000-0002-7071-6763
Jingyu YangDepartment of Mammary Gland and Thyroid Disease, First People's Hospital of Yunnan Province, Yunnan, China.ORCID 0000-0002-6376-3983
Ying LuoLaboratory of Molecular Genetics of Aging & Tumor, Medical School, Kunming University of Science and Technology, Yunnan, China.ORCID 0000-0002-5366-8704
Wenru TangLaboratory of Molecular Genetics of Aging & Tumor, Medical School, Kunming University of Science and Technology, Yunnan, China.ORCID 0000-0002-7231-037X
Miaomiao ShengLaboratory of Molecular Genetics of Aging & Tumor, Medical School, Kunming University of Science and Technology, Yunnan, China.ORCID 0000-0001-6341-8939
Kunming Medical University · CNFirst People's Hospital of Yunnan Province · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeBreast cancer is the most frequently diagnosed malignancy in women worldwide. MicroRNAs (miRNAs) are thought to serve as potential biomarkers in various cancers, including breast cancer.

methodsWe evaluated the miRNA expression profiles in 1,083 breast cancer samples and 104 normal breast tissues from The Cancer Genome Atlas database. We used the edgeR package of R software to analyze the differentially expressed miRNAs in normal and cancer tissues, and screened survival-related miRNAs by Kaplan-Meier analysis. A receiver operating characteristic curve was generated to evaluate the accuracy of these miRNAs as molecular markers for breast cancer diagnosis. Furthermore, the functional role of these miRNAs was verified using cell experiments. Targets of candidate miRNAs were predicted using 9 online databases, and Gene Ontology (GO) functional annotation and pathway analyses were conducted using Database for Annotation, Visualization and Integrated Discovery online tool.

resultsA total of 68 miRNAs showed significantly different expression patterns between the groups (

conclusionThe miR-148b-3p, miR-190b, and miR-429 may serve as potential diagnostic and prognostic markers for breast cancer. This study demonstrated the roles of these 3 miRNAs in the initiation and progression of breast cancer.

Indexed as

Biological markerBiological phenomenonBreast neoplasmMicroRNA

Identifiers

PMID31281725
PMCPMC6597412
OpenAlexW2941154109

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.