Evidence map›Paper›PMID 25291178›Full record

ArticlePloS one2014

Autonomous stimulation of cancer cell plasticity by the human NKG2D lymphocyte receptor coexpressed with its ligands on cancer cells.

Xin Cai, Zhenpeng Dai, Rebecca S Reeves, Andrea Caballero-Benitez, Kate L Duran, Jeffrey J Delrow, Peggy L Porter, Thomas Spies, Veronika Groh

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
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

9 authors at 1 institution in 1 country.

Xin CaiClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Zhenpeng DaiClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Rebecca S ReevesClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Andrea Caballero-BenitezClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Kate L DuranClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Jeffrey J DelrowClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Peggy L PorterHuman Biology Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Thomas SpiesClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Veronika GrohClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Fred Hutch Cancer Center · US

Funding

Vaccinating against IGFBP-2 to prevent ovarian cancer relapseP50CA083636 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI DRESCHER, CHARLES, URBAN, NICOLE DENISE · 1999 to 2015
$35.1M
Stimulation of Tumorigenesis by NKG2DR01CA174470 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI SPIES, THOMAS · 2013 to 2017
$3.1M
NCI NIH HHS P50 CA083636NCI NIH HHS R01 CA174470
6 · The paper itself

Abstract

The stimulatory NKG2D receptor on lymphocytes promotes tumor immune surveillance by targeting ligands selectively induced on cancer cells. Progressing tumors counteract by employing tactics to disable lymphocyte NKG2D. This negative dynamic is escalated as some human cancer cells co-opt expression of NKG2D, thereby complementing the presence of its ligands for autonomous stimulation of oncogenic signaling. Clinical association data imply relationships between cancer cell NKG2D and metastatic disease. Here we show that NKG2D promotes cancer cell plasticity by induction of phenotypic, molecular, and functional signatures diagnostic of the epithelial-mesenchymal transition, and of stem-like traits via induction of Sox9, a key transcriptional regulator of breast stem cell maintenance. These findings obtained with model breast tumor lines and xenotransplants were recapitulated by ex vivo cancer cells from primary invasive breast carcinomas. Thus, NKG2D may have the capacity to drive high malignancy traits underlying metastatic disease.

Indexed as

Gene ExpressionLigandsAnimalsCell Line, TumorDisease Models, AnimalEpithelial-Mesenchymal TransitionHeterograftsHumansMiceNeoplasmsNeoplastic Stem CellsNK Cell Lectin-Like Receptor Subfamily KPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReceptors, ImmunologicHCST protein, humanLigandsNK Cell Lectin-Like Receptor Subfamily KPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReceptors, Immunologic

Identifiers

PMID25291178
PMCPMC4188595
OpenAlexW1973553933

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.