Evidence map›Paper›PMID 22246988›Full record

ArticleEMBO molecular medicine2012

N-myc downstream regulated gene 1 modulates Wnt-β-catenin signalling and pleiotropically suppresses metastasis.

Wen Liu, Fei Xing, Megumi Iiizumi-Gairani, Hiroshi Okuda, Misako Watabe, Sudha K Pai, Puspa R Pandey, Shigeru Hirota, Aya Kobayashi, Yin-Yuan Mo and 3 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed
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

95 citing papers in PubMed, 199 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. The inhibition of YTHDF3/mInternational journal of biological sciences · 2024
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Increased Expression of the Δ133p53β Isoform Enhances Brain Metastasis.International journal of molecular sciences · 2023
    Article
  13. Review
  14. Review
  15. Article
  16. Response to de Nonneville, Finetti, Mamessier, and Bertucci.Journal of the National Cancer Institute · 2022
    Article
  17. NDRG1 in Aggressive Breast Cancer Progression and Brain Metastasis.Journal of the National Cancer Institute · 2022
    Article
  18. Article
  19. Article
  20. Article

35 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

13 authors at 3 institutions in 2 countries.

Wen LiuDepartment of Medical Microbiology, Southern Illinois University School of Medicine, Springfield, IL, USA.
Fei Xing
Megumi Iiizumi-Gairani
Hiroshi Okuda
Misako Watabe
Sudha K Pai
Puspa R Pandey
Shigeru Hirota
Aya Kobayashi
Yin-Yuan Mo
Koji Fukuda
Yi Li
Kounosuke Watabe
Southern Illinois University School of Medicine · USBaylor College of Medicine · USIwate Medical University · JP

Funding

Mechanism of tumor metastases suppression by Drg1R01CA124650 · NCI · UNIVERSITY OF MISSISSIPPI MED CTR · PI WATABE, KOUNOSUKE · 2007 to 2012
$1.1M
Functional role of tumor metastases suppressor gene, KAl1, in tumor progressionR01CA129000 · NCI · UNIVERSITY OF MISSISSIPPI MED CTR · PI WATABE, KOUNOSUKE · 2007 to 2012
$1.0M
NCI NIH HHS R01 CA124650NCI NIH HHS R01CA124650NCI NIH HHS R01 CA129000NCI NIH HHS R01CA129000
6 · The paper itself

Abstract

Wnt signalling has pivotal roles in tumour progression and metastasis; however, the exact molecular mechanism of Wnt signalling in the metastatic process is as yet poorly defined. Here we demonstrate that the tumour metastasis suppressor gene, NDRG1, interacts with the Wnt receptor, LRP6, followed by blocking of the Wnt signalling, and therefore, orchestrates a cellular network that impairs the metastatic progression of tumour cells. Importantly, restoring NDRG1 expression by a small molecule compound significantly suppressed the capability of otherwise highly metastatic tumour cells to thrive in circulation and distant organs in animal models. In addition, our analysis of clinical cohorts data indicate that Wnt+/NDRG-/LRP+ signature has a strong predictable value for recurrence-free survival of cancer patients. Collectively, we have identified NDRG1 as a novel negative master regulator of Wnt signalling during the metastatic progression, which opens an opportunity to define a potential therapeutic target for metastatic disease.

Indexed as

Animalsbeta CateninCell Cycle ProteinsCells, CulturedGenes, mycHEK293 CellsHumansIntracellular Signaling Peptides and ProteinsMiceMice, SCIDNeoplasm MetastasisN-myc Downstream-Regulated Gene 1 ProteinSignal TransductionTransfectionWnt Proteinsbeta CateninCell Cycle ProteinsIntracellular Signaling Peptides and ProteinsN-myc Downstream-Regulated Gene 1 ProteinWnt Proteins

Identifiers

PMID22246988
PMCPMC3306556
OpenAlexW2153654059

What OpenQuestion holds

Textmetadata
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.