Evidence map›Paper›PMID 42106562›Full record

ArticleCommunications biology2026

Aggressive breast cancers secrete heme metabolites to alter macrophage immune suppression and function.

Michelle M Williams, Jessica L Christenson, Nicole S Spoelstra, Sabrina A Hafeez, Li-Wei Kuo, Lyndsey S Crump, Kathleen I O'Neill, Alexis A Hill, Angelica Phan, Lauren M McCue and 8 more

Abstract read
In one paragraph

Article in Communications biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

18 authors.

Michelle M WilliamsDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA. mmw178@pitt.edu.ORCID http://orcid.org/0000-0002-7063-9147
Jessica L ChristensonDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.ORCID http://orcid.org/0000-0002-6311-8191
Nicole S SpoelstraDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Sabrina A HafeezDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Li-Wei KuoDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Lyndsey S CrumpDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Kathleen I O'NeillDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Alexis A HillDepartment of Pharmacology and Chemical Biology, University of Pittsburgh, Pittsburgh, PA, USA.ORCID http://orcid.org/0009-0003-3544-6686
Angelica PhanDepartment of Pharmacology and Chemical Biology, University of Pittsburgh, Pittsburgh, PA, USA.ORCID http://orcid.org/0009-0003-2210-7191
Lauren M McCueDepartment of Pharmacology and Chemical Biology, University of Pittsburgh, Pittsburgh, PA, USA.
Thomas M HintelmannDepartment of Pharmacology and Chemical Biology, University of Pittsburgh, Pittsburgh, PA, USA.
Juanantonio RuizDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Haley E SaxDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Jared WilliamsDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.ORCID http://orcid.org/0000-0003-2082-8553
Meher Preethi BoorgulaUniversity of Colorado Cancer Center, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Andrew GoodspeedUniversity of Colorado Cancer Center, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Jill E SlanskyUniversity of Colorado Cancer Center, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.ORCID http://orcid.org/0000-0003-3820-1724
Jennifer K RicherDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.ORCID http://orcid.org/0000-0002-9960-0991

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHRISTOPHER J. BAKKENIST · 1988 to 2026
$158.0M
University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
Training Program in Cancer BiologyT32CA190216 · NCI · UNIVERSITY OF COLORADO DENVER · PI Craig T. Jordan · 2016 to 2026
$3.5M
Targeting heme metabolism to initiate an immune response against breast cancer liver metastasisR00CA266748 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Michelle M Williams · 2024 to 2026
$731k
Targeting heme metabolism to initiate an immune response against breast cancer liver metastasisK99CA266748 · NCI · UNIVERSITY OF COLORADO DENVER · PI WILLIAMS, MICHELLE M · 2022 to 2023
$229k
Impact of heme catabolism on triple negative breast cancer metastasis via immune-suppressionF32CA239436 · NCI · UNIVERSITY OF COLORADO DENVER · PI WILLIAMS, MICHELLE M · 2020 to 2021
$142k
NCI NIH HHS F32 CA239436NCI NIH HHS K99 CA266748NCI NIH HHS P30 CA046934NCI NIH HHS P30 CA047904NCI NIH HHS R00 CA266748NCI NIH HHS T32 CA190216U.S. Department of Defense (United States Department of Defense) W81XWH-19-BCRP-EAU.S. Department of Defense (United States Department of Defense) W81XWH-20-1-0617U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) F32CA239436U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) K99R00CA266748
6 · The paper itself

Abstract

The heme catabolism pathway is often elevated in aggressive cancers; however, the impact of this pathway and some of its byproducts on the tumor microenvironment remain largely unknown. In human breast cancers, tumor expression of the heme catabolizing enzyme heme oxygenase-1 (HO-1/HMOX1) is positively associated with macrophage abundance. In mouse mammary tumors, knockdown of Hmox1 significantly decreased tumor growth and lung metastasis. Analysis of mammary tumor interstitial fluid compared to matching plasma revealed that the heme metabolite bilirubin was elevated intratumorally, which could be partially reversed via Hmox1 knockdown. Further investigation revealed that bilirubin nearly ablates macrophage engulfment of dead tumor cells and significantly increases macrophage T cell suppression. Mammary tumors harboring Hmox1 knockdown had a significant decrease in tumor growth rate and number of pro-metastatic CD206

Indexed as

Breast NeoplasmsHemeMacrophagesAnimalsBilirubinCell Line, TumorFemaleHeme Oxygenase-1HumansMiceTumor MicroenvironmentBilirubinHemeHeme Oxygenase-1

Identifiers

PMID42106562
PMCPMC13376764

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.