Evidence map›Paper›PMID 38821060›Full record

ArticleCancer cell2024

The temporal progression of lung immune remodeling during breast cancer metastasis.

Christopher S McGinnis, Zhuang Miao, Daphne Superville, Winnie Yao, Andrei Goga, Nathan E Reticker-Flynn, Juliane Winkler, Ansuman T Satpathy

Abstract read
In one paragraph

Article in Cancer cell, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing 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

49 citing papers in PubMed.

  1. Review
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  8. Dual-pathway induction of pyroptosisActa pharmaceutica Sinica. B · 2026
    Article
  9. Article
  10. Review
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  13. Review
  14. Article
  15. Altered Erythrocyte Function via TLR9-ox-mtDNA Binding Links Mitochondrial Oxidative Damage to Systemic Inflammation in Multiple Sclerosis.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    Article
  16. Article
  17. The Ly6gCancer communications (London, England) · 2026
    Article
  18. Review
  19. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Christopher S McGinnisDepartment of Pathology, Stanford University, Stanford, CA 94305, USA; Gladstone-UCSF Institute of Genomic Immunology, San Francisco, CA 94158, USA; Parker Institute for Cancer Immunotherapy, San Francisco, CA 94129, USA.
Zhuang MiaoDepartment of Pathology, Stanford University, Stanford, CA 94305, USA; Gladstone-UCSF Institute of Genomic Immunology, San Francisco, CA 94158, USA.
Daphne SupervilleHelen Diller Family Comprehensive Cancer Center, UCSF, San Francisco, CA 94158, USA; Department of Cell and Tissue Biology, UCSF, San Francisco, CA 94143, USA; Department of Medicine, UCSF, San Francisco, CA 94143, USA.
Winnie YaoDepartment of Pathology, Stanford University, Stanford, CA 94305, USA; Gladstone-UCSF Institute of Genomic Immunology, San Francisco, CA 94158, USA.
Andrei GogaHelen Diller Family Comprehensive Cancer Center, UCSF, San Francisco, CA 94158, USA; Department of Cell and Tissue Biology, UCSF, San Francisco, CA 94143, USA; Department of Medicine, UCSF, San Francisco, CA 94143, USA.
Nathan E Reticker-FlynnDepartment of Otolaryngology, Stanford University, Stanford, CA 94305, USA.
Juliane WinklerCenter for Cancer Research, Medical University of Vienna, Vienna 1090, Austria. Electronic address: juliane.winkler@meduniwien.ac.at.
Ansuman T SatpathyDepartment of Pathology, Stanford University, Stanford, CA 94305, USA; Gladstone-UCSF Institute of Genomic Immunology, San Francisco, CA 94158, USA; Parker Institute for Cancer Immunotherapy, San Francisco, CA 94129, USA. Electronic address: satpathy@stanford.edu.

Funding

4DN Interrogation of T Cell Exhaustion in CancerU01CA260852 · NCI · STANFORD UNIVERSITY · PI SATPATHY, ANSUMAN · 2020 to 2024
$2.6M
Defining a novel subset of metastasis-associated monocytesF31CA284749 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SUPERVILLE, DAPHNE A · 2023 to 2024
$91k
NCI NIH HHS F31 CA284749NCI NIH HHS U01 CA260852
6 · The paper itself

Abstract

Tumor metastasis requires systemic remodeling of distant organ microenvironments that impacts immune cell phenotypes, population structure, and intercellular communication. However, our understanding of immune phenotypic dynamics in the metastatic niche remains incomplete. Here, we longitudinally assayed lung immune transcriptional profiles in the polyomavirus middle T antigen (PyMT) and 4T1 metastatic breast cancer models from primary tumorigenesis, through pre-metastatic niche formation, to the final stages of metastatic outgrowth at single-cell resolution. Computational analyses of these data revealed a TLR-NFκB inflammatory program enacted by both peripherally derived and tissue-resident myeloid cells that correlated with pre-metastatic niche formation and mirrored CD14

Indexed as

Breast NeoplasmsKiller Cells, NaturalLung NeoplasmsTumor MicroenvironmentAnimalsCell Line, TumorChemokines, CCDisease ProgressionFemaleGene Expression Regulation, NeoplasticHumansInsulin-Like Growth Factor ILungMiceMice, Inbred BALB CMyeloid CellsChemokines, CCInsulin-Like Growth Factor Icancer immunologyimmunosuppressioninflammationmetastasismyeloidnatural killer cellsNF-κBsingle-cell genomicsTLR

Identifiers

PMID38821060
PMCPMC11255555

What OpenQuestion 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 OpenQuestion graph.