Evidence map›Paper›PMID 22496624›Full record

ArticleNeoplasia (New York, N.Y.)2012

Apoptosis resistance and PKC signaling: distinguishing features of high and low metastatic cells.

Sung-Hyeok Hong, Ling Ren, Arnulfo Mendoza, Ananth Eleswarapu, Chand Khanna

Open access · goldAbstract read
In one paragraph

Article in Neoplasia (New York, N.Y.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

17 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Pharmacologic Inhibition of EIF4A Blocks NRF2 Synthesis to Prevent Osteosarcoma Metastasis.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Article
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  4. Novel role of the dietary flavonoid fisetin in suppressing rRNA biogenesis.Laboratory investigation; a journal of technical methods and pathology · 2021
    Article
  5. NSG Mice FacilitateFrontiers in oncology · 2021
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. mTOR Inhibition Mitigates Enhanced mRNA Translation Associated with the Metastatic Phenotype of Osteosarcoma Cells In Vivo.Clinical cancer research : an official journal of the American Association for Cancer Research · 2016
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. 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

5 authors at 2 institutions in 1 country.

Sung-Hyeok HongTumor and Metastasis Biology Section, Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Ling Ren
Arnulfo Mendoza
Ananth Eleswarapu
Chand Khanna
Center for Cancer Research · USNational Cancer Institute · US

Funding

Tumor and Metastasis BiologyZIABC010566 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HELMAN, LEE J. · 2009 to 2017
$4.6M
Tumor and Metastasis TherapyZIABC011024 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KHANNA, CHAND · 2009 to 2013
$3.2M
Intramural NIH HHS
6 · The paper itself

Abstract

The complexity of the process of metastasis is widely recognized. We report herein on a recurrent feature of high compared to low metastatic cells that is linked to their ability to survive early after their arrival at secondary sites. Using novel fluorescent-based imaging strategies that assess tumor cell interaction with the lung microenvironment, we have determined that most high and low metastatic cells can be distinguished within 6 hours of their arrival in the lung and further that this difference is defined by the ability of high metastatic cells to resist apoptosis at the secondary site. Despite the complexity of the metastatic cascade, the performance of cells during this critical window is highly defining of their metastatic proclivity. To explore mechanisms, we next evaluated biochemical pathways that may be linked to this survival phenotype in highly metastatic cells. Interestingly, we found no association between the Akt survival pathway and this metastatic phenotype. Of all pathways examined, only protein kinase C (PKC) activation was significantly linked to survival of highly metastatic cells. These data provide a conceptual understanding of a defining difference between high and low metastatic cells. The connection to PKC activation may provide a biologic rationale for the use of PKC inhibition in the prevention of metastatic progression.

Indexed as

ApoptosisSignal TransductionAnimalsCell Line, TumorCell ProliferationFemaleHumansLung NeoplasmsMiceMice, Inbred BALB CNeoplasmsPhenotypeProtein Kinase CProtein Kinase InhibitorsProto-Oncogene Proteins c-aktProtein Kinase CProtein Kinase InhibitorsProto-Oncogene Proteins c-akt

Identifiers

PMID22496624
PMCPMC3323902
OpenAlexW1950298337

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.