Evidence map›Paper›PMID 23492819›Full record

ArticleCarcinogenesis2013

MicroRNA-93 regulates NRF2 expression and is associated with breast carcinogenesis.

Bhupendra Singh, Amruta M Ronghe, Anwesha Chatterjee, Nimee K Bhat, Hari K Bhat

Open access · bronzeAbstract read
In one paragraph

Article in Carcinogenesis, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

91 citing papers in PubMed, 197 citations in OpenAlex.

  1. Trial
  2. International journal of molecular sciences · 2026
    Review
  3. Article
  4. Review
  5. Review
  6. Effects of Clinical Covariates on Serum miRNA Expression among Women without Ovarian Cancer.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2025
    Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Review
  12. MiRNA-93: a novel signature in human disorders and drug resistance.Cell communication and signaling : CCS · 2023
    Review
  13. Article
  14. Review
  15. Review
  16. Emerging role of miRNAs in the regulation of ferroptosis.Frontiers in molecular biosciences · 2023
    Review
  17. Review
  18. Review
  19. Review
  20. Regulation of Ferroptosis by Non-Coding RNAs in Head and Neck Cancers.International journal of molecular sciences · 2022
    Review

31 more citing papers are in PubMed but not listed here.

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

5 authors at 1 institution in 1 country.

Bhupendra SinghDivision of Pharmacology and Toxicology, School of Pharmacy, University of Missouri-Kansas City, Kansas City, MO 64108, USA.
Amruta M Ronghe
Anwesha Chatterjee
Nimee K Bhat
Hari K Bhat
University of Missouri–Kansas City · US

Funding

Molecular Mechanisms & Importance of Oxidative Stress in Estrogen-Induced CarcinoR01CA109551 · NCI · UNIVERSITY OF MISSOURI KANSAS CITY · PI BHAT, HARI K · 2006 to 2011
$1.1M
NCI NIH HHS CA109551
6 · The paper itself

Abstract

MicroRNAs (miRNA) are small non-coding RNAs that regulate the expression of approximately 60% of all human genes and play important roles in disease processes. Recent studies have demonstrated a link between dysregulated expression of miRNAs and breast carcinogenesis. Long-term estrogen exposure is implicated in development of human breast cancers, yet underlying mechanisms remain elusive. We have recently demonstrated that antioxidant vitamin C (vit C) prevents estrogen-induced breast tumor development. In this study, we investigated the role of vit C in the regulation of microRNA-93 (miR-93) and its target gene(s) in a rat model of mammary carcinogenesis. Female August Copenhagen Irish (ACI) rats were treated with vit C in the presence or absence of 17β-estradiol (E2) for 8 months. We demonstrate an increased expression of the miR-93 in E2-treated mammary tissues and in human breast cell lines and vit C treatment reverted E2-mediated increase in miR-93 levels. MiRNA target prediction programs suggest one of the target genes of miR-93 to be nuclear factor erythroid 2-related factor 2 (NRF2). In contrast with miR-93 expression, NRF2 protein expression was significantly decreased in E2-treated mammary tissues, mammary tumors, and in breast cancer cell lines, and its expression was significantly increased after vit C treatment. Ectopic expression of miR-93 decreased protein expression of NRF2 and NRF2-regulated genes. Furthermore, miR-93 decreased apoptosis, increased colony formation, mammosphere formation, cell migration and DNA damage in breast epithelial cells, whereas silencing of miR-93 in these cells inhibited these carcinogenic processes. Taken together, our findings suggest an oncogenic potential of miR-93 during E2-induced breast carcinogenesis.

Indexed as

AnimalsApoptosisAscorbic AcidBreast NeoplasmsCell Line, TumorCell MovementCell Transformation, NeoplasticDNA DamageEstradiolEstrogensFemaleHumansMicroRNAsNF-E2-Related Factor 2RatsRats, Inbred ACIAscorbic AcidEstradiolEstrogensMicroRNAsNF-E2-Related Factor 2

Identifiers

PMID23492819
PMCPMC3643421
OpenAlexW2116439283

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.