Evidence map›Paper›PMID 28545025›Full record

ArticleOncotarget2017

Oncogenic MNK signalling regulates the metastasis suppressor NDRG1.

Shuye Tian, Xuemin Wang, Christopher G Proud

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. 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
1.0field-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, 23 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. NDRG1 in Aggressive Breast Cancer Progression and Brain Metastasis.Journal of the National Cancer Institute · 2022
    Article
  6. SGK1, autophagy and cancer: an overview.Molecular biology reports · 2022
    Review
  7. Article
  8. Article
  9. Deeping in the Role of the MAP-Kinases Interacting Kinases (MNKs) in Cancer.International journal of molecular sciences · 2020
    Review
  10. Article
  11. Review
  12. Article
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

3 authors at 2 institutions in 1 country.

Shuye TianNutrition and Metabolism, South Australian Health and Medical Research Institute, Adelaide SA5000, Australia.
Xuemin WangNutrition and Metabolism, South Australian Health and Medical Research Institute, Adelaide SA5000, Australia.
Christopher G ProudNutrition and Metabolism, South Australian Health and Medical Research Institute, Adelaide SA5000, Australia.
South Australian Health and Medical Research Institute · AUUniversity of Adelaide · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The protein N-myc down-regulated gene 1 (NDRG1) represses tumour metastasis. It is phosphorylated at several sites by serum and glucocorticoid-regulated kinase 1 (SGK1). Here we show that NDRG1 is also regulated by the oncogenic MAP kinase-interacting kinase (MNK) pathway, a target for cancer therapy.Inhibiting MNKs increases the expression of NDRG1 protein and mRNA in breast cancer cells. MNK inhibition also decreases the phosphorylation of NDRG1. Phosphorylation of NDRG1 is reduced in cells lacking MNK1, but not MNK2-knockout cells, indicating that NDRG1 phosphorylation is a specific target for MNK1. However, MNK1 cannot directly phosphorylate NDRG1 in vitro, indicating that additional signalling connections are involved. Taken together, our data indicate that MNK signaling regulates NDRG1 at transcriptional and post-translational levels.We show that SGK1 phosphorylates MNK1 at a conserved site, which represses its activity. NDRG1, SGK1 and the MNKs are implicated in cell migration and metastasis. As expected, knocking-down NDRG1 promoted cell migration. However, whereas MNK inhibition impairs these processes irrespective of NDRG1 levels, SGK inhibition only did so in NDRG1-depleted cells. Thus, MNKs and SGK affect migration/invasion through distinct mechanisms.Our data reveal several novel connections between signalling pathways important for tumour biology.

Indexed as

AnimalsBreast NeoplasmsCarcinogenesisCell Cycle ProteinsCell Line, TumorCell MovementFemaleGene Expression Regulation, NeoplasticHumansImmediate-Early ProteinsIntracellular Signaling Peptides and ProteinsMiceNeoplasm MetastasisN-myc Downstream-Regulated Gene 1 ProteinPhosphorylationProtein Processing, Post-TranslationalCell Cycle ProteinsImmediate-Early ProteinsIntracellular Signaling Peptides and ProteinsMKNK1 protein, humanMknk1 protein, mouseN-myc Downstream-Regulated Gene 1 ProteinProtein Serine-Threonine KinasesRNA, Small InterferingSerum-Glucocorticoid Regulated Kinasesbreast cancermigrationMNK1NDRG1SGK

Identifiers

PMID28545025
PMCPMC5542254
OpenAlexW2610316222

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.