Evidence map›Paper›PMID 29643230›Full record

ArticleScience translational medicine2018

The systemic response to surgery triggers the outgrowth of distant immune-controlled tumors in mouse models of dormancy.

Jordan A Krall, Ferenc Reinhardt, Oblaise A Mercury, Diwakar R Pattabiraman, Mary W Brooks, Michael Dougan, Arthur W Lambert, Brian Bierie, Hidde L Ploegh, Stephanie K Dougan and 1 more

Abstract read
In one paragraph

Article in Science translational medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 249 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
249citing papers in PubMed, 1 pooled it
–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

249 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  18. Achieving protease substrate-specific inhibition by mAb dual functional selections.Protein science : a publication of the Protein Society · 2026
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189 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Jordan A KrallWhitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.ORCID 0000-0002-7851-6600
Ferenc ReinhardtWhitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.
Oblaise A MercuryWhitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.ORCID 0000-0002-8853-7560
Diwakar R PattabiramanWhitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.
Mary W BrooksWhitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.
Michael DouganWhitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.
Arthur W LambertWhitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.ORCID 0000-0002-2989-7961
Brian BierieWhitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.
Hidde L PloeghWhitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.ORCID 0000-0002-1090-6071
Stephanie K DouganWhitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.
Robert A WeinbergWhitehead Institute for Biomedical Research, Cambridge, MA 02142, USA. weinberg@wi.mit.edu.ORCID 0000-0002-0895-3557

Funding

Regulation of brown fat metabolism by the immune receptor PD-L1K08DK114563 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI DOUGAN, MICHAEL LAWRENCE · 2017 to 2021
$868k
Exploiting the epithelial-to-mesenchymal transition for the differentiation of cancer stem cellsK99CA201574 · NCI · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI PATTABIRAMAN, DIWAKAR R · 2016 to 2017
$202k
NCI NIH HHS K99 CA201574NIDDK NIH HHS K08 DK114563
6 · The paper itself

Abstract

Patients undergoing surgical resection of primary breast tumors confront a risk for metastatic recurrence that peaks sharply 12 to 18 months after surgery. The cause of early metastatic relapse in breast cancer has long been debated, with many ascribing these relapses to the natural progression of the disease. Others have proposed that some aspect of surgical tumor resection triggers the outgrowth of otherwise-dormant metastases, leading to the synchronous pattern of relapse. Clinical data cannot distinguish between these hypotheses, and previous experimental approaches have not provided clear answers. Such uncertainty hinders the development and application of therapeutic approaches that could potentially reduce early metastatic relapse. We describe an experimental model system that definitively links surgery and the subsequent wound-healing response to the outgrowth of tumor cells at distant anatomical sites. Specifically, we find that the systemic inflammatory response induced after surgery promotes the emergence of tumors whose growth was otherwise restricted by a tumor-specific T cell response. Furthermore, we demonstrate that perioperative anti-inflammatory treatment markedly reduces tumor outgrowth in this model, suggesting that similar approaches might substantially reduce early metastatic recurrence in breast cancer patients.

Indexed as

AnimalsBiomarkers, TumorBreast NeoplasmsCD8-Positive T-LymphocytesCell Line, TumorFemaleMiceNeoplasm MetastasisNeoplasm Recurrence, LocalBiomarkers, Tumor

Identifiers

PMID29643230
PMCPMC6364295

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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.