Evidence map›Paper›PMID 21860426›Full record

ArticleOncogene2012

MicroRNA-mediated upregulation of integrin-linked kinase promotes Src-induced tumor progression.

C Oneyama, E Morii, D Okuzaki, Y Takahashi, J Ikeda, N Wakabayashi, H Akamatsu, M Tsujimoto, T Nishida, K Aozasa and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
2.8field-weighted citation impact, top 11% 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

41 citing papers in PubMed, 72 citations in OpenAlex.

  1. Article
  2. Assessment ofInternational journal of molecular sciences · 2023
    Article
  3. Article
  4. Article
  5. Integrin-linked kinase (ILK): the known vs. the unknown and perspectives.Cellular and molecular life sciences : CMLS · 2022
    Review
  6. Article
  7. Review
  8. Historical retrospective of theMolecular and clinical oncology · 2020
    Review
  9. Article
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  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
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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

11 authors at 2 institutions in 1 country.

C OneyamaDepartment of Oncogene Research, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan. coneyama@biken.osaka-u.ac.jp
E Morii
D Okuzaki
Y Takahashi
J Ikeda
N Wakabayashi
H Akamatsu
M Tsujimoto
T Nishida
K Aozasa
M Okada
Osaka University · JPOsaka Police Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tyrosine kinase c-Src is upregulated in various human cancers; however, the molecular mechanisms underlying c-Src-mediated tumor progression remain unclear. Here we show that downregulation of microRNA (miR)-542-3p is tightly associated with tumor progression via c-Src-related oncogenic pathways. In c-Src-transformed fibroblasts and human cancer cells that overexpress c-Src, miR-542-3p is substantially downregulated, and the ectopic expression of miR-542-3p suppresses tumor growth. We identified the integrin-linked kinase (ILK) as a conserved target of miR-542-3p. ILK upregulation promotes cell adhesion and invasion by activating the integrin-focal adhesion kinase (FAK)/c-Src pathway, and can also contribute to tumor growth via the AKT and glycogen synthase kinase 3β pathways. MiR-542-3p expression is downregulated by the activation of c-Src-related signaling molecules, including epidermal growth factor receptor, K-Ras and Ras/Raf/mitogen-activated protein kinase/extracellular signal-regulated kinase. In human colon cancer tissues, downregulation of miR-542-3p is significantly correlated with the upregulation of c-Src and ILK. Our results suggest that the novel c-Src-miR-542-3p-ILK-FAK circuit plays a crucial role in controlling tumor progression.

Indexed as

AnimalsCell AdhesionCell LineColonic NeoplasmsCSK Tyrosine-Protein KinaseDisease ProgressionFocal Adhesion Kinase 1HumansMiceMicroRNAsNeoplasm InvasivenessNeoplasmsProtein Serine-Threonine KinasesProtein-Tyrosine KinasesScaffold Protein ILKsrc-Family KinasesCSK protein, humanCSK Tyrosine-Protein KinaseFocal Adhesion Kinase 1MicroRNAsMIRN542 microRNA, mouseProtein Serine-Threonine KinasesProtein-Tyrosine KinasesScaffold Protein ILKsrc-Family Kinases

Identifiers

PMID21860426
OpenAlexW1992716524

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.