Evidence map›Paper›PMID 30154549›Full record

ArticleNature cell biology2018

IL-1β inflammatory response driven by primary breast cancer prevents metastasis-initiating cell colonization.

Zafira Castaño, Beatriz P San Juan, Asaf Spiegel, Ayush Pant, Molly J DeCristo, Tyler Laszewski, Jessalyn M Ubellacker, Susanne R Janssen, Anushka Dongre, Ferenc Reinhardt and 8 more

Abstract read
In one paragraph

Article in Nature cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 107 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
107citing papers in PubMed, 2 pooled it
7.9field-weighted citation impact, top 2% 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

107 citing papers in PubMed, 2 syntheses or guidelines pooled it, 165 citations in OpenAlex.

  1. Pooled it
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  11. NF-κB in inflammation and cancer.Cellular & molecular immunology · 2025
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47 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

18 authors at 7 institutions in 2 countries.

Zafira CastañoDivision of Hematology, Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Beatriz P San JuanThe Kinghorn Cancer Centre, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.
Asaf SpiegelWhitehead Institute for Biomedical Research, Cambridge, MA, USA.
Ayush PantWhitehead Institute for Biomedical Research, Cambridge, MA, USA.
Molly J DeCristoDivision of Hematology, Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Tyler LaszewskiDivision of Hematology, Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Jessalyn M UbellackerDivision of Hematology, Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Susanne R JanssenWhitehead Institute for Biomedical Research, Cambridge, MA, USA.
Anushka DongreWhitehead Institute for Biomedical Research, Cambridge, MA, USA.
Ferenc ReinhardtWhitehead Institute for Biomedical Research, Cambridge, MA, USA.
Ayana HendersonDivision of Hematology, Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Ana Garcia Del RioDivision of Hematology, Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Ann M GiffordWhitehead Institute for Biomedical Research, Cambridge, MA, USA.
Zachary T HerbertMolecular Biology Core Facilities, Dana-Farber Cancer Institute, Boston, MA, USA.
John N HutchinsonDepartment of Biostatistics, Harvard T.H. Chan, School of Public Health, Boston, MA, USA.
Robert A WeinbergWhitehead Institute for Biomedical Research, Cambridge, MA, USA.
Christine L ChafferThe Kinghorn Cancer Centre, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia. c.chaffer@garvan.org.au.ORCID http://orcid.org/0000-0003-2620-6130
Sandra S McAllisterDivision of Hematology, Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA. smcallister1@bwh.harvard.edu.ORCID http://orcid.org/0000-0002-5111-5903
Brigham and Women's Hospital · USWhitehead Institute for Biomedical Research · USGarvan Institute of Medical Research · AUBroad Institute · USDana-Farber Cancer Institute · USHarvard University · USIIT@MIT · US

Funding

VectorP30CA006516 · NCI · DANA-FARBER CANCER INSTITUTE · PI JENNIFER W MACK · 1985 to 2026
$330.6M
Diversity in Biomedical Sciences Via Personalized Research and Education Programs for Post-BaccalaureatesR25GM109436 · NIGMS · HARVARD UNIVERSITY · PI D'SOUZA, VICTORIA MANUEL, VELEZ-RUIZ, GISSELLE A · 2016 to 2024
$2.5M
Understanding How Breast Cancers Activate and Respond to the Systemic EnvironmentR01CA166284 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI MCALLISTER, SANDRA S · 2012 to 2018
$2.2M
NCI NIH HHS P30 CA006516NCI NIH HHS R01 CA166284NIGMS NIH HHS R25 GM109436
6 · The paper itself

Abstract

Lack of insight into mechanisms governing breast cancer metastasis has precluded the development of curative therapies. Metastasis-initiating cancer cells (MICs) are uniquely equipped to establish metastases, causing recurrence and therapeutic resistance. Using various metastasis models, we discovered that certain primary tumours elicit a systemic inflammatory response involving interleukin-1β (IL-1β)-expressing innate immune cells that infiltrate distant MIC microenvironments. At the metastatic site, IL-1β maintains MICs in a ZEB1-positive differentiation state, preventing MICs from generating highly proliferative E-cadherin-positive progeny. Thus, when the inherent plasticity of MICs is impeded, overt metastases cannot be established. Ablation of the pro-inflammatory response or inhibition of the IL-1 receptor relieves the differentiation block and results in metastatic colonization. Among patients with lymph node-positive breast cancer, high primary tumour IL-1β expression is associated with better overall survival and distant metastasis-free survival. Our data reveal complex interactions that occur between primary tumours and disseminated MICs that could be exploited to improve patient survival.

Indexed as

Tumor MicroenvironmentAnimalsAntigens, CDAnti-Inflammatory AgentsBreast NeoplasmsCadherinsCell CommunicationCell DifferentiationCell Line, TumorCell PlasticityCell ProliferationFemaleHumansInflammationInterleukin-1betaLung NeoplasmsAntigens, CDAnti-Inflammatory AgentsCadherinsCDH1 protein, humanIL1B protein, humanIL1B protein, mouseInterleukin-1betaZEB1 protein, humanZinc Finger E-box-Binding Homeobox 1

Identifiers

PMID30154549
PMCPMC6511979
OpenAlexW2888320733

What OpenQuestion holds

Textmetadata
LicenceTDM
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.