Evidence mapPaperPMID 39859445Full record

ArticleInternational journal of molecular sciences2025

Soy Isoflavone Genistein Enhances Tamoxifen Sensitivity in Breast Cancer via microRNA and Glucose Metabolism Modulation.

Jessica Shpigel, Emilia F Luciano, Blessing Ukandu, Moira Sauane, Columba de la Parra

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

5 authors.

Jessica ShpigelDepartment of Chemistry, Herbert H. Lehman College, City University of New York, New York, NY 10468, USA.
Emilia F LucianoDepartment of Chemistry, Herbert H. Lehman College, City University of New York, New York, NY 10468, USA.ORCID 0009-0004-9787-1300
Blessing UkanduDepartment of Chemistry, Herbert H. Lehman College, City University of New York, New York, NY 10468, USA.
Moira SauaneDepartment of Biological Sciences, Herbert H. Lehman College, City University of New York, New York, NY 10468, USA.ORCID 0000-0003-2710-3491
Columba de la ParraDepartment of Chemistry, Herbert H. Lehman College, City University of New York, New York, NY 10468, USA.ORCID 0000-0002-5438-8157

Funding

U-RISE at Lehman CollegeT34GM149385 · HERBERT H. LEHMAN COLLEGE · 2025 to 2025
$237k
Translation Initiation Inhibitor for Cancer TherapyR16GM145561 · HERBERT H. LEHMAN COLLEGE · 2025 to 2025
$143k
The role of an alternate mechanism of translation initiation in TNBC MetabolismR16GM153947 · HERBERT H. LEHMAN COLLEGE · 2025 to 2025
$138k
National Institute of General Medical Sciences of the National Institutes of Health R16GM153947NIGMS NIH HHS R16 GM145561NIGMS NIH HHS R16 GM153947NIGMS NIH HHS T34 GM149385
6 · The paper itself

Abstract

Breast cancer treatment has advanced significantly, particularly for estrogen receptor-positive (ER+) tumors. Tamoxifen, an estrogen antagonist, is widely used; however, approximately 40% of patients develop resistance. Recent studies indicate that microRNAs, especially miR-155, play a critical role in this resistance. Our analysis of MCF-7 tamoxifen-sensitive (TAM-S) and tamoxifen-resistant (TAM-R) cells revealed that miR-155 is significantly upregulated in TAM-R cells. Overexpression of miR-155 in TAM-S cells increased resistance to tamoxifen. Additionally, genistein, a natural isoflavone from soybeans, effectively downregulated miR-155 and its targets associated with apoptosis and glucose metabolism, including STAT3 and hexokinase 2 (HK2). Notably, genistein also significantly decreased cell migration, suggesting potential anti-metastatic effects. Furthermore, genistein reduced glucose consumption, indicating its potential to overcome miR-155-mediated tamoxifen resistance and modulate the Warburg effect. These findings highlight genistein as a promising therapeutic agent for overcoming tamoxifen resistance in ER+ breast cancer and merit further investigation.

Indexed as

Breast NeoplasmsDrug Resistance, NeoplasmGenisteinGlucoseGlycine maxMicroRNAsTamoxifenApoptosisCell Line, TumorCell MovementFemaleGene Expression Regulation, NeoplasticHexokinaseHumansMCF-7 CellsSTAT3 Transcription FactorGenisteinGlucoseHexokinaseHK2 protein, humanMicroRNAsMIRN155 microRNA, humanSTAT3 Transcription FactorTamoxifenbreast cancergenisteinglucose metabolismisoflavonemicroRNAnatural compoundstamoxifen

Identifiers

PMID39859445
PMCPMC11765730

What Socratic holds

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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 Socratic graph.