Evidence map›Paper›PMID 38815010›Full record

ArticleScience (New York, N.Y.)2024

Germline-mediated immunoediting sculpts breast cancer subtypes and metastatic proclivity.

Kathleen E Houlahan, Aziz Khan, Noah F Greenwald, Cristina Sotomayor Vivas, Robert B West, Michael Angelo, Christina Curtis

Abstract read
PubMed Publisher
In one paragraph

Article in Science (New York, N.Y.), 2024. 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.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Kathleen E HoulahanStanford Cancer Institute, Stanford University School of Medicine, Stanford, CA, 94305, USA.ORCID 0000-0002-2273-2099
Aziz KhanStanford Cancer Institute, Stanford University School of Medicine, Stanford, CA, 94305, USA.ORCID 0000-0002-6459-6224
Noah F GreenwaldCancer Biology Program, Stanford University School of Medicine, Stanford, CA, 94305, USA.ORCID 0000-0002-7836-4379
Cristina Sotomayor VivasStanford Cancer Institute, Stanford University School of Medicine, Stanford, CA, 94305, USA.ORCID 0000-0001-8228-477X
Robert B WestDepartment of Pathology, Stanford University School of Medicine, Stanford, CA, 94305, USA.ORCID 0000-0002-8330-8283
Michael AngeloDepartment of Pathology, Stanford University School of Medicine, Stanford, CA, 94305, USA.ORCID 0000-0003-1531-5067
Christina CurtisStanford Cancer Institute, Stanford University School of Medicine, Stanford, CA, 94305, USA.ORCID 0000-0003-0166-3802

Funding

Stanford Breast Metastasis Center Administrative CoreU54CA261719 · NCI · STANFORD UNIVERSITY · PI Christina N Curtis · 2021 to 2026
$8.6M
Forecasting tumor evolution: can the past reveal the future?DP1CA238296 · NCI · STANFORD UNIVERSITY · PI CURTIS, CHRISTINA N · 2018 to 2022
$5.5M
NCI NIH HHS DP1 CA238296NCI NIH HHS U54 CA261719
6 · The paper itself

Abstract

Tumors with the same diagnosis can have different molecular profiles and response to treatment. It remains unclear when and why these differences arise. Somatic genomic aberrations occur within the context of a highly variable germline genome. Interrogating 5870 breast cancer lesions, we demonstrated that germline-derived epitopes in recurrently amplified genes influence somatic evolution by mediating immunoediting. Individuals with a high germline-epitope burden in human epidermal growth factor receptor 2 (HER2/

Indexed as

Breast NeoplasmsClonal EvolutionErb-b2 Receptor Tyrosine KinasesGerm-Line MutationEpitopesFemaleGerm CellsHumansNeoplasm MetastasisReceptors, EstrogenEpitopesERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesReceptors, Estrogen

Identifiers

What OpenQuestion holds

Textmetadata
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.