Evidence map›Paper›PMID 28562349›Full record

ArticleOncotarget2017

MicroRNA-155, induced by FOXP3 through transcriptional repression of BRCA1, is associated with tumor initiation in human breast cancer.

Song Gao, Yicun Wang, Meng Wang, Zhi Li, Zhiying Zhao, Raymond X Wang, Rong Wu, Zhengwei Yuan, Ranji Cui, Kai Jiao and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 3 pooled it
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.

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

30 citing papers in PubMed, 3 syntheses or guidelines pooled it, 39 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Article
  6. Potential biological roles of exosomal non-coding RNAs in breast cancer.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Review
  7. Review
  8. MicroRNA-155-5p, Reduced by Curcumin-Re-Expressed HypermethylatedInternational journal of molecular sciences · 2023
    Article
  9. Review
  10. Article
  11. Review
  12. Forkhead Box Protein P3 (FOXP3) Represses ATF3 Transcriptional Activity.International journal of molecular sciences · 2021
    Article
  13. [Role of exosomal miRNA in tumor progression and its possible mechanism].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2021
    Article
  14. Review
  15. Article
  16. Impact ofFrontiers in oncology · 2021
    Article
  17. Review
  18. Review
  19. Review
  20. Review
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

13 authors at 6 institutions in 2 countries.

Song GaoThe Second Department of Clinical Oncology, Shengjing Hospital of China Medical University, Shenyang, China.
Yicun WangProvincial Key Laboratory on Molecular and Chemical Genetic, Second Hospital of Jilin University, Changchun, China.
Meng WangDepartment of Oncology, Cancer Hospital of Harbin Medical University, Harbin, China.
Zhi LiDepartment of General Surgery, Henan Cancer Hospital, Zhengzhou, China.
Zhiying ZhaoSchool of Computer Science and Engineering, Northeastern University, Shenyang, China.
Raymond X WangDepartment of Genetics, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Rong WuThe Second Department of Clinical Oncology, Shengjing Hospital of China Medical University, Shenyang, China.
Zhengwei YuanThe Second Department of Clinical Oncology, Shengjing Hospital of China Medical University, Shenyang, China.
Ranji CuiProvincial Key Laboratory on Molecular and Chemical Genetic, Second Hospital of Jilin University, Changchun, China.
Kai JiaoDepartment of Genetics, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Lizhong WangDepartment of Genetics, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Ling OuyangDepartment of Gynecology and Obstetrics, Shengjing Hospital of China Medical University, Shenyang, China.
Runhua LiuDepartment of Genetics, University of Alabama at Birmingham, Birmingham, Alabama, USA.
China Medical University · CNUniversity of Alabama at Birmingham · USSecond Affiliated Hospital of Jilin University · CNHarbin Medical University · CNHenan Cancer Hospital · CNNortheastern University · CN

Funding

XRAY CRYSTALLOGRAPHYP30CA013148 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Robert S Welner · 1985 to 2026
$165.9M
UAB Center for Clinical and Translational Science (CCTS)UL1TR001417 · NCATS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KIMBERLY, ROBERT P. · 2015 to 2018
$31.4M
TRAINING AND CAREER DEVELOPMENTU54CA118948 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Timiya S Nolan · 2005 to 2026
$26.6M
Research Education CoreU54CA118623 · NCI · TUSKEGEE UNIVERSITY · PI STEPHEN O SODEKE · 2005 to 2026
$20.2M
INFRASTRUCTURE IIG12MD007585 · NIMHD · TUSKEGEE UNIVERSITY · PI YATES, CLAYTON · 2012 to 2016
$4.6M
Roles of Semaphorin Signaling in Breast Cancer Racial DisparitiesR21CA199586 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI JIAO, KAI, WANG, LIZHONG · 2015 to 2016
$352k
MicroRNAs for monitoring tumor progression and predicting response to therapyR21CA179282 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI WANG, LIZHONG · 2014 to 2015
$352k
NCATS NIH HHS UL1 TR001417NCI NIH HHS P30 CA013148NCI NIH HHS R21 CA179282NCI NIH HHS R21 CA199586NCI NIH HHS U54 CA118623NCI NIH HHS U54 CA118948NIMHD NIH HHS G12 MD007585
6 · The paper itself

Abstract

MicroRNA (miR)-155 is upregulated in breast cancer cells and in sera of patients with breast cancer, but its clinical relevance remains uncertain. The objective of the present effort was to address the transcriptional regulation of miR-155. A bioinformatics analysis of public datasets validated upregulation of miR-155 in tumor cells of patients with breast cancer, particularly those who were at early stages and had triple-negative cancers. The expression profiling and clinical relevance of miR-155 in tumor cells and blood cells were characterized by TaqMan miR assays and, in plasma and exosomes, by nest-quantitative PCR analysis. There was a positive correlation between expression of FOXP3 and miR-155 in breast cancer cell lines and primary breast cancers. In breast cancer cells, FOXP3 induced miR-155 through transcriptional repression of BRCA1. Furthermore, in an Alabama cohort, blood and plasma samples were collected from 259 participants, including patients with breast cancer or benign breast tumors, members of breast cancer families, and matched healthy female controls. For patients with early stage or localized breast cancer, there were high levels of miR-155 in both plasma and blood cells. In cultured breast cancer cells, expression of miR-155 was induced by FOXP3 but was not significantly changed in culture medium or exosomes, suggesting that circulating miR-155 originated from blood cells. These findings reveal a transcriptional axis of FOXP3-BRCA1-miR-155 in breast cancer cells and show that plasma miR-155 may serve as a non-invasive biomarker for detection of early stage breast cancer.

Indexed as

Gene Expression Regulation, NeoplasticAdultAgedBiomarkers, TumorBRCA1 ProteinBreast NeoplasmsCell LineCell Line, TumorCohort StudiesForkhead Transcription FactorsGene Expression ProfilingHumansMCF-7 CellsMicroRNAsMiddle AgedTriple Negative Breast NeoplasmsBiomarkers, TumorBRCA1 ProteinBRCA1 protein, humanForkhead Transcription FactorsFOXP3 protein, humanMicroRNAsMIRN155 microRNA, humanBRCA1breast cancerFOXP3microRNAplasma

Identifiers

PMID28562349
PMCPMC5522316
OpenAlexW2613445533

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.