Evidence map›Paper›PMID 30341686›Full record

ReviewJournal of cancer research and clinical oncology2018

The concept of the okadaic acid class of tumor promoters is revived in endogenous protein inhibitors of protein phosphatase 2A, SET and CIP2A, in human cancers.

Hirota Fujiki, Eisaburo Sueoka, Tatsuro Watanabe, Masami Suganuma

Open access · hybridAbstract readReview
In one paragraph

Review in Journal of cancer research and clinical oncology, 2018. 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
1.9field-weighted citation impact, top 14% 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, 43 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
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  7. Article
  8. ModelingEnvironmental and ecological statistics · 2022
    Article
  9. Review
  10. Article
  11. SET levels contribute to cohesion fatigue.Molecular biology of the cell · 2021
    Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. 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

4 authors at 2 institutions in 1 country.

Hirota FujikiFaculty of Medicine, Saga University, Nabeshima, Saga, 849-8501, Japan. uv4h-fjk@asahi-net.or.jp.ORCID http://orcid.org/0000-0002-1512-3551
Eisaburo SueokaFaculty of Medicine, Saga University, Nabeshima, Saga, 849-8501, Japan.
Tatsuro WatanabeFaculty of Medicine, Saga University, Nabeshima, Saga, 849-8501, Japan.
Masami SuganumaGraduate School of Science and Engineering, Saitama University, Saitama, 338-8570, Japan.
Saga University · JPSaitama University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe okadaic acid class of tumor promoters, which are inhibitors of protein phosphatases 1 and 2A (PP1 and PP2A), induced tumor promotion in mouse skin, rat glandular stomach, and rat liver. Endogenous protein inhibitors of PP2A, SET and CIP2A, were up-regulated in various human cancers, so it is vital to review the essential mechanisms of tumor promotion by the okadaic acid class compounds, together with cancer progression by SET and CIP2A in humans. RESULTS AND DISCUSSION: The first part of this review introduces the okadaic acid class compounds and the mechanism of tumor promotion: (1) inhibition of PP1 and PP2A activities of the okadaic acid class compounds; (2) some topics of tumor promotion; (3) TNF-α gene expression as a central mediator in tumor promotion; (4) exposure to the okadaic acid class of tumor promoters in relation to human cancer. The second part emphasizes the overexpression of SET and CIP2A in cancer progression, and the anticancer activity of SET antagonists as follows: (5) isolation and characterization of SET; (6) isolation and characterization of CIP2A; (7) progression of leukemia with SET; (8) progression of breast cancer with SET and CIP2A; (9) progression of lung cancer with SET; (10) anti-carcinogenic effects of SET antagonists OP449 and FTY720; and also (11) TNF-α-inducing protein of Helicobacter pylori, which is a clinical example of the okadaic acid pathway.

conclusionsThe overexpression of endogenous protein inhibitors of PP2A, SET and CIP2A, is tightly linked to the progression of various human cancers, as well as Alzheimer's disease.

Indexed as

AnimalsAutoantigensBiomarkers, TumorCell Transformation, NeoplasticDisease ProgressionDNA-Binding ProteinsEnvironmental ExposureEnzyme InhibitorsGene Expression Regulation, NeoplasticHelicobacter InfectionsHelicobacter pyloriHistone ChaperonesHumansIntracellular Signaling Peptides and ProteinsMembrane ProteinsMolecular Targeted TherapyAutoantigensBiomarkers, TumorCIP2A protein, humanDNA-Binding ProteinsEnzyme InhibitorsHistone ChaperonesIntracellular Signaling Peptides and ProteinsMembrane ProteinsOkadaic AcidProtein Phosphatase 2SET protein, humanTranscription FactorsTumor Necrosis Factor-alphaCIP2AOkadaic acidPP1PP2ASETTipαTNF-α

Identifiers

PMID30341686
PMCPMC6244643
OpenAlexW2895955401

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.