Evidence map›Paper›PMID 27530323›Full record

ArticleCancer research2016

Inflammation Triggers Zeb1-Dependent Escape from Tumor Latency.

Jasmine M De Cock, Tsukasa Shibue, Anushka Dongre, Zuzana Keckesova, Ferenc Reinhardt, Robert A Weinberg

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 106 papers.

0numbers the graph read from it
0cells of the map it votes in
106citing papers in PubMed
9.0field-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

106 citing papers in PubMed, 149 citations in OpenAlex.

  1. Review
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  9. Inflammation awakens dormant cancer cells by modulating the epithelial-mesenchymal phenotypic state.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  10. Review
  11. Article
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  17. Mouse Models of Metastasis and Dormancy.Cold Spring Harbor perspectives in medicine · 2024
    Review
  18. Review
  19. Dormancy of cutaneous melanoma.Cancer cell international · 2024
    Review
  20. Article

46 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

6 authors at 1 institution in 1 country.

Jasmine M De CockWhitehead Institute for Biomedical Research, Cambridge, Massachusetts.
Tsukasa ShibueWhitehead Institute for Biomedical Research, Cambridge, Massachusetts.
Anushka DongreWhitehead Institute for Biomedical Research, Cambridge, Massachusetts.
Zuzana KeckesovaWhitehead Institute for Biomedical Research, Cambridge, Massachusetts.
Ferenc ReinhardtWhitehead Institute for Biomedical Research, Cambridge, Massachusetts.
Robert A WeinbergWhitehead Institute for Biomedical Research, Cambridge, Massachusetts. weinberg@wi.mit.edu.
Massachusetts Institute of Technology · US

Funding

Use of Organotypic and Mammary Gland Models to Investigate the Outcomes of ClonalP01CA080111 · NCI · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI DILLON, DEBORAH · 1999 to 2018
$36.0M
Induced Differentiation to Deplete CSCs from Breast CancerR01CA078461 · NCI · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI WEINBERG, ROBERT A · 1999 to 2017
$8.5M
The Extracellular Matrix in Tumor Progression and MetastasisU54CA163109 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI WEINBERG, ROBERT A · 2011 to 2015
$3.7M
NCI NIH HHS P01 CA080111NCI NIH HHS R01 CA078461NCI NIH HHS U54 CA163109
6 · The paper itself

Abstract

The emergence of metastatic disease in cancer patients many years or decades after initial successful treatment of primary tumors is well documented but poorly understood at the molecular level. Recent studies have begun exploring the cell-intrinsic programs, causing disseminated tumor cells to enter latency and the cellular signals in the surrounding nonpermissive tissue microenvironment that maintain the latent state. However, relatively little is known about the mechanisms that enable disseminated tumor cells to escape cancer dormancy or tumor latency. We describe here an in vivo model of solitary metastatic latency in the lung parenchyma. The induction of a localized inflammation in the lungs, initiated by lipopolysaccharide treatment, triggers the awakening of these cells, which develop into macroscopic metastases. The escape from latency is dependent on the expression of Zeb1, a key regulator of the epithelial-to-mesenchymal transition (EMT). Furthermore, activation of the EMT program on its own, as orchestrated by Zeb1, is sufficient to incite metastatic outgrowth by causing carcinoma cells to enter stably into a metastasis-initiating cell state. Cancer Res; 76(23); 6778-84. ©2016 AACR.

Indexed as

AnimalsCell Line, TumorCell ProliferationHumansInflammationMiceNeoplasm MetastasisSignal TransductionZinc Finger E-box-Binding Homeobox 1ZEB1 protein, mouseZinc Finger E-box-Binding Homeobox 1

Identifiers

PMID27530323
PMCPMC5135644
OpenAlexW2515910706

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.