Evidence map›Paper›PMID 39779850›Full record

ArticleNature2025

Complex rearrangements fuel ER

Kathleen E Houlahan, Lise Mangiante, Cristina Sotomayor-Vivas, Alvina Adimoelja, Seongyeol Park, Aziz Khan, Sophia J Pribus, Zhicheng Ma, Jennifer L Caswell-Jin, Christina Curtis

Abstract read
In one paragraph

Article in Nature, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
  2. Ultrasound-activated RuORSC advances · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Targeting extrachromosomal DNA in human cancers.Nature reviews. Drug discovery · 2026
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  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

10 authors.

Kathleen E Houlahan *Stanford Cancer Institute, School of Medicine, Stanford University, Stanford, CA, USA.ORCID 0000-0002-2273-2099
Lise Mangiante *Stanford Cancer Institute, School of Medicine, Stanford University, Stanford, CA, USA.ORCID 0000-0001-8309-0950
Cristina Sotomayor-Vivas *Stanford Cancer Institute, School of Medicine, Stanford University, Stanford, CA, USA.ORCID 0000-0001-8228-477X
Alvina Adimoelja *Department of Genetics, School of Medicine, Stanford University, Stanford, CA, USA.
Seongyeol ParkStanford Cancer Institute, School of Medicine, Stanford University, Stanford, CA, USA.
Aziz KhanStanford Cancer Institute, School of Medicine, Stanford University, Stanford, CA, USA.ORCID 0000-0002-6459-6224
Sophia J PribusStanford Cancer Institute, School of Medicine, Stanford University, Stanford, CA, USA.
Zhicheng MaStanford Cancer Institute, School of Medicine, Stanford University, Stanford, CA, USA.
Jennifer L Caswell-JinDepartment of Medicine (Oncology), School of Medicine, Stanford University, Stanford, CA, USA.ORCID 0000-0002-5711-8355
Christina CurtisStanford Cancer Institute, School of Medicine, Stanford University, Stanford, CA, USA. cncurtis@stanford.edu.ORCID 0000-0003-0166-3802

Funding

Stanford Breast Metastasis Center Administrative CoreU54CA261719 · NCI · STANFORD UNIVERSITY · PI Christina N Curtis · 2021 to 2026
$8.6M
Integrative subtyping to improve therapeutic options for metastatic hormone receptor-positive breast cancerK08CA252457 · NCI · STANFORD UNIVERSITY · PI CASWELL-JIN, JENNIFER · 2020 to 2024
$1.1M
NCI NIH HHS K08 CA252457NCI NIH HHS U54 CA261719Wellcome Trust
6 · The paper itself

Abstract

Breast cancer is a highly heterogeneous disease whose prognosis and treatment as defined by the expression of three receptors-oestrogen receptor (ER), progesterone receptor and human epidermal growth factor receptor 2 (HER2; encoded by ERBB2)-is insufficient to capture the full spectrum of clinical outcomes and therapeutic vulnerabilities. Previously, we demonstrated that transcriptional and genomic profiles define eleven integrative subtypes with distinct clinical outcomes, including four ER

Indexed as

Breast NeoplasmsErb-b2 Receptor Tyrosine KinasesGene RearrangementReceptors, EstrogenCohort StudiesFemaleGene AmplificationGenomic InstabilityHumansTriple Negative Breast NeoplasmsERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesReceptors, Estrogen

Identifiers

PMID39779850
PMCPMC11821522

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.