Evidence map›Paper›PMID 29324443›Full record

ArticleThe Journal of clinical investigation2018

Epithelial-mesenchymal transition leads to NK cell-mediated metastasis-specific immunosurveillance in lung cancer.

Peter J Chockley, Jun Chen, Guoan Chen, David G Beer, Theodore J Standiford, Venkateshwar G Keshamouni

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 102 papers.

0numbers the graph read from it
0cells of the map it votes in
102citing 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

102 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. IL1RAJournal of clinical and translational hepatology · 2025
    Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Natural killer cells: the immune frontline against circulating tumor cells.Journal of experimental & clinical cancer research : CR · 2025
    Review
  12. Article
  13. CD56Journal for immunotherapy of cancer · 2025
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Peter J ChockleyDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine.
Jun ChenDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine.
Guoan ChenDepartment of Surgery, University of Michigan Medical Center, Ann Arbor, Michigan, USA.
David G BeerDepartment of Surgery, University of Michigan Medical Center, Ann Arbor, Michigan, USA.
Theodore J StandifordDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine.
Venkateshwar G KeshamouniDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine.

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI THEODORE S LAWRENCE · 1988 to 2026
$178.2M
RESEARCH TRAINING IN EXPERIMENTAL IMMUNOPATHOLOGYT32AI007413 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Bethany B. Moore · 1993 to 2026
$9.8M
Novel IL-1 Family Members in Lung Innate ImmunityR01HL123515 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI STANDIFORD, THEODORE J. · 2015 to 2018
$2.5M
Regulation of Tumor Associated Macrophages by TGF-betaR01CA132571 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KESHAMOUNI, VENKATESHWAR G · 2008 to 2012
$1.4M
NCI NIH HHS P30 CA046592NCI NIH HHS R01 CA132571NHLBI NIH HHS R01 HL123515NIAID NIH HHS T32 AI007413
6 · The paper itself

Abstract

During epithelial-mesenchymal transition (EMT) epithelial cancer cells transdifferentiate into highly motile, invasive, mesenchymal-like cells, giving rise to disseminating tumor cells. Few of these disseminated cells successfully metastasize. Immune cells and inflammation in the tumor microenvironment were shown to drive EMT, but few studies investigated the consequences of EMT for tumor immunosurveillance. In addition to initiating metastasis, we demonstrate that EMT confers increased susceptibility to natural killer (NK) cells and contributes, in part, to the inefficiency of the metastatic process. Depletion of NK cells allowed spontaneous metastasis without affecting primary tumor growth. EMT-induced modulation of E-cadherin and cell adhesion molecule 1 (CADM1) mediated increased susceptibility to NK cytotoxicity. Higher CADM1 expression correlates with improved patient survival in 2 lung and 1 breast adenocarcinoma patient cohorts and decreased metastasis. Our observations reveal a novel NK-mediated, metastasis-specific immunosurveillance in lung cancer and present a window of opportunity for preventing metastasis by boosting NK cell activity.

Indexed as

Immunity, CellularImmunologic SurveillanceA549 CellsAnimalsCarcinoma, Lewis LungCell Adhesion Molecule-1Epithelial-Mesenchymal TransitionFemaleHumansKiller Cells, NaturalLung NeoplasmsMaleMiceMice, KnockoutNeoplasm ProteinsTumor MicroenvironmentCADM1 protein, humanCadm1 protein, mouseCell Adhesion Molecule-1Neoplasm ProteinsImmunologyImmunotherapyLung cancerNK cellsOncology

Identifiers

PMID29324443
PMCPMC5873856

What OpenQuestion holds

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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.