Evidence map›Paper›PMID 38593809›Full record

ArticleCell reports. Medicine2024

Pharmacological induction of chromatin remodeling drives chemosensitization in triple-negative breast cancer.

Meisam Bagheri, Gadisti Aisha Mohamed, Mohammed Ashick Mohamed Saleem, Nevena B Ognjenovic, Hanxu Lu, Fred W Kolling, Owen M Wilkins, Subhadeep Das, Ian S LaCroix, Shivashankar H Nagaraj and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports. Medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

14 citing papers in PubMed, 16 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. High-Efficiency Genomic Mapping of Chromatin-Associated Targets with CUT&RUN.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. EMT and cancer: what clinicians should know.Nature reviews. Clinical oncology · 2025
    Review
  13. Review
  14. 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

14 authors at 2 institutions in 2 countries.

Meisam BagheriDepartment of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Lebanon, NH, USA.
Gadisti Aisha MohamedDepartment of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Lebanon, NH, USA.
Mohammed Ashick Mohamed SaleemLifebytes India Pvt. Ltd., Bengaluru, India.
Nevena B OgnjenovicDepartment of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Lebanon, NH, USA.
Hanxu LuDepartment of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Lebanon, NH, USA.
Fred W KollingCenter for Quantitative Biology, Geisel School of Medicine at Dartmouth, Lebanon, NH, USA.
Owen M WilkinsCenter for Quantitative Biology, Geisel School of Medicine at Dartmouth, Lebanon, NH, USA.
Subhadeep DasLifebytes India Pvt. Ltd., Bengaluru, India.
Ian S LaCroixDepartment of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Lebanon, NH, USA.
Shivashankar H NagarajCentre for Genomics and Personalised Health, School of Biomedical Sciences, Faculty of Health, Queensland University of Technology, Brisbane, QLD, Australia; Translational Research Institute, Brisbane, QLD 4102, Australia.
Kristen E MullerDepartment of Pathology, Geisel School of Medicine at Dartmouth, Lebanon, NH, USA.
Scott A GerberDepartment of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Lebanon, NH, USA.
Todd W MillerDepartment of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Lebanon, NH, USA; Department of Pharmacology & Toxicology, Medical College of Wisconsin, Milwaukee, WI, USA; Department of Pathology, Medical College of Wisconsin, Milwaukee, WI, USA. Electronic address: tomiller@mcw.edu.
Diwakar R PattabiramanDepartment of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Lebanon, NH, USA. Electronic address: diwakar.r.pattabiraman@dartmouth.edu.
Dartmouth College · USTranslational Research Institute · AU

Funding

Translational Engineering in Cancer (TEC)P30CA023108 · NCI · DARTMOUTH COLLEGE · PI Steven D Leach · 1985 to 2026
$91.3M
Zhao - Proj 2P20GM130454 · NIGMS · DARTMOUTH COLLEGE · PI Chengxiang Qiu · 2019 to 2026
$27.2M
Therapeutically leveraging metabolic vulnerabilities in breast cancerR01CA262232 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Todd W. Miller · 2022 to 2026
$2.2M
Uncovering the basis and implications of lineage plasticity in breast cancerR01CA267691 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Todd W. Miller · 2022 to 2026
$1.8M
Defining human kinase-substrate networks and their dynamic regulationR01GM122846 · NIGMS · DARTMOUTH COLLEGE · PI GERBER, SCOTT A. · 2017 to 2020
$1.5M
Exploiting the epithelial-to-mesenchymal transition for the differentiation of cancer stem cellsR00CA201574 · NCI · DARTMOUTH COLLEGE · PI PATTABIRAMAN, DIWAKAR R · 2018 to 2020
$686k
Acquisition of the NextSeq2000 Sequencing platform to Increase Next Generation Sequencing Throughput While Reducing Costs at DartmouthS10OD030242 · OD · DARTMOUTH COLLEGE · PI KOLLING IV, FRED W · 2021 to 2021
$321k
10X Genomics Chromium Single-cell Sequencing to Expand Research At DartmouthS10OD025235 · OD · DARTMOUTH COLLEGE · PI TOMLINSON, CRAIG R · 2018 to 2018
$125k
NCI NIH HHS P30 CA023108NCI NIH HHS R00 CA201574NCI NIH HHS R01 CA262232NCI NIH HHS R01 CA267691NIGMS NIH HHS P20 GM130454NIGMS NIH HHS R01 GM122846NIH HHS S10 OD025235NIH HHS S10 OD030242
6 · The paper itself

Abstract

Targeted therapies have improved outcomes for certain cancer subtypes, but cytotoxic chemotherapy remains a mainstay for triple-negative breast cancer (TNBC). The epithelial-to-mesenchymal transition (EMT) is a developmental program co-opted by cancer cells that promotes metastasis and chemoresistance. There are no therapeutic strategies specifically targeting mesenchymal-like cancer cells. We report that the US Food and Drug Administration (FDA)-approved chemotherapeutic eribulin induces ZEB1-SWI/SNF-directed chromatin remodeling to reverse EMT that curtails the metastatic propensity of TNBC preclinical models. Eribulin induces mesenchymal-to-epithelial transition (MET) in primary TNBC in patients, but conventional chemotherapy does not. In the treatment-naive setting, but not after acquired resistance to other agents, eribulin sensitizes TNBC cells to subsequent treatment with other chemotherapeutics. These findings provide an epigenetic mechanism of action of eribulin, supporting its use early in the disease process for MET induction to prevent metastatic progression and chemoresistance. These findings warrant prospective clinical evaluation of the chemosensitizing effects of eribulin in the treatment-naive setting.

Indexed as

Antineoplastic AgentsFuransKetonesPolyether PolyketidesTriple Negative Breast NeoplasmsChromatin Assembly and DisassemblyHumansProspective StudiesUnited StatesAntineoplastic AgentseribulinFuransKetonesPolyether Polyketidesbreast cancerchemotherapydrug resistanceEMTepigeneticepithelial-to-mesenchymal transitionmesenchymal-to-epithelial transitionmetastasis

Identifiers

PMID38593809
PMCPMC11031425
OpenAlexW4394567665

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.