Evidence map›Paper›PMID 37756565›Full record

ArticleCancer discovery2023

Spatial and Temporal Mapping of Breast Cancer Lung Metastases Identify TREM2 Macrophages as Regulators of the Metastatic Boundary.

Ido Yofe, Tamar Shami, Noam Cohen, Tomer Landsberger, Fadi Sheban, Liat Stoler-Barak, Adam Yalin, Truong San Phan, Baoguo Li, Lea Monteran and 9 more

Open access · greenAbstract read
In one paragraph

Article in Cancer discovery, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 88 papers.

0numbers the graph read from it
0cells of the map it votes in
88citing papers in PubMed
17.8field-weighted citation impact, top 1% 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

88 citing papers in PubMed, 102 citations in OpenAlex.

  1. Review
  2. Review
  3. The immunology of human breast cancer.Nature reviews. Immunology · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

28 more citing papers are in PubMed but not listed here.

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

19 authors at 2 institutions in 1 country.

Ido Yofe *Department of Systems Immunology, Weizmann Institute of Science, Rehovot, Israel.ORCID 0009-0004-4747-7057
Tamar Shami *Department of Pathology, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.ORCID 0009-0007-2014-4297
Noam Cohen *Department of Pathology, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.ORCID 0009-0003-7047-8843
Tomer Landsberger *Department of Systems Immunology, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0001-6926-2648
Fadi ShebanDepartment of Systems Immunology, Weizmann Institute of Science, Rehovot, Israel.ORCID 0009-0008-2819-6953
Liat Stoler-BarakDepartment of Systems Immunology, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0001-8194-9979
Adam YalinDepartment of Systems Immunology, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0001-7161-6126
Truong San PhanDepartment of Systems Immunology, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0002-8837-5119
Baoguo LiDepartment of Systems Immunology, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0001-9276-7943
Lea MonteranDepartment of Pathology, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.ORCID 0000-0002-7633-2090
Ye'ela ScharffDepartment of Pathology, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.ORCID 0000-0002-4886-9923
Amir GiladiDepartment of Systems Immunology, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0002-5880-2845
Miriam ElbazDepartment of Systems Immunology, Weizmann Institute of Science, Rehovot, Israel.ORCID 0009-0005-2127-1162
Eyal DavidDepartment of Systems Immunology, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0002-9020-2364
Anna Gurevich-ShapiroDepartment of Systems Immunology, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0001-9698-1306
Chamutal GurDepartment of Systems Immunology, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0001-5191-2956
Ziv ShulmanDepartment of Systems Immunology, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0002-9604-212X
Neta ErezDepartment of Pathology, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.ORCID 0000-0001-6506-9074
Ido AmitDepartment of Systems Immunology, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0003-2968-877X
Weizmann Institute of Science · ILTel Aviv University · IL

Funding

Emerson Collective (Emerson)European Research Council 101055341HORIZON EUROPE European Research Council (ERC) 101055341-TROJAN-CellIsrael Cancer Research Fund (ICRF)Israel Science Foundation (ISF) 1090/18Israel Science Foundation (ISF) #3495/19U.S. Department of Defense (DOD) W81XWH2110394Worldwide Cancer Research 20-0169Worldwide Cancer Research (WCR)
6 · The paper itself

Abstract

Cancer mortality primarily stems from metastatic recurrence, emphasizing the urgent need for developing effective metastasis-targeted immunotherapies. To better understand the cellular and molecular events shaping metastatic niches, we used a spontaneous breast cancer lung metastasis model to create a single-cell atlas spanning different metastatic stages and regions. We found that premetastatic lungs are infiltrated by inflammatory neutrophils and monocytes, followed by the accumulation of suppressive macrophages with the emergence of metastases. Spatial profiling revealed that metastasis-associated immune cells were present in the metastasis core, with the exception of TREM2+ regulatory macrophages uniquely enriched at the metastatic invasive margin, consistent across both murine models and human patient samples. These regulatory macrophages (Mreg) contribute to the formation of an immune-suppressive niche, cloaking tumor cells from immune surveillance. Our study provides a compendium of immune cell dynamics across metastatic stages and niches, informing the development of metastasis-targeting immunotherapies. SIGNIFICANCE: Temporal and spatial single-cell analysis of metastasis stages revealed new players in modulating immune surveillance and suppression. Our study highlights distinct populations of TREM2 macrophages as modulators of the microenvironment in metastasis, and as the key immune determinant defining metastatic niches, pointing to myeloid checkpoints to improve therapeutic strategies. This article is featured in Selected Articles from This Issue, p. 2489.

Indexed as

Breast NeoplasmsLung NeoplasmsAnimalsFemaleHumansLungMacrophagesMembrane GlycoproteinsMiceNeoplasm MetastasisReceptors, ImmunologicTumor MicroenvironmentMembrane GlycoproteinsReceptors, ImmunologicTREM2 protein, human

Identifiers

PMID37756565
PMCPMC7617931
OpenAlexW4387088536

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.