Evidence map›Paper›PMID 24121273›Full record

ArticleOncogene2014

Oncogenic suppression of PHLPP1 in human melanoma.

L Dong, L Jin, H-Y Tseng, C Y Wang, J S Wilmott, B Yosufi, X G Yan, C C Jiang, R A Scolyer, X D Zhang and 1 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

25 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The Essential Oil fromPharmaceuticals (Basel, Switzerland) · 2023
    Article
  5. Article
  6. Article
  7. Article
  8. PHLPP Signaling in Immune Cells.Current topics in microbiology and immunology · 2022
    Review
  9. Article
  10. PHLPPing the Script: Emerging Roles of PHLPP Phosphatases in Cell Signaling.Annual review of pharmacology and toxicology · 2021
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

11 authors at 3 institutions in 2 countries.

L DongSchool of Medicine and Public Health, The University of Newcastle, Newcastle, NSW, Australia.
L JinSchool of Medicine and Public Health, The University of Newcastle, Newcastle, NSW, Australia.
H-Y TsengSchool of Medicine and Public Health, The University of Newcastle, Newcastle, NSW, Australia.
C Y WangDepartment of Molecular Biology, Shanxi Cancer Hospital and Institute, Affiliated Hospital of Shanxi Medical University, Taiyuan, China.
J S Wilmott1] Melanoma Institute Australia, Sydney, NSW, Australia [2] Discipline of Pathology, The University of Sydney, Sydney, NSW, Australia.
B YosufiMelanoma Institute Australia, Sydney, NSW, Australia.
X G YanSchool of Medicine and Public Health, The University of Newcastle, Newcastle, NSW, Australia.
C C JiangSchool of Medicine and Public Health, The University of Newcastle, Newcastle, NSW, Australia.
R A Scolyer1] Melanoma Institute Australia, Sydney, NSW, Australia [2] Discipline of Pathology, The University of Sydney, Sydney, NSW, Australia [3] Tissue Pathology and Diagnostic Oncology, Royal Prince Alfred Hospital, Sydney, NSW, Australia.
X D ZhangSchool of Medicine and Public Health, The University of Newcastle, Newcastle, NSW, Australia.
S T GuoDepartment of Molecular Biology, Shanxi Cancer Hospital and Institute, Affiliated Hospital of Shanxi Medical University, Taiyuan, China.
University of Newcastle Australia · AUMelanoma Institute Australia · AUShanxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Akt is constitutively activated in up to 70% of human melanomas and has an important role in the pathogenesis of the disease. However, little is known about protein phosphatases that dephosphorylate and thereby inactivate it in melanoma cells. Here we report that suppression of pleckstrin homology domain and leucine-rich repeat Ser/Thr protein phosphatase 1 (PHLPP1) by DNA methylation promotes Akt activation and has an oncogenic role in melanoma. While it is commonly downregulated, overexpression of PHLPP1 reduces Akt activation and inhibits melanoma cell proliferation in vitro, and retards melanoma growth in a xenograft model. In contrast, knockdown of PHLPP1 increases Akt activation, enhances melanoma cell and melanocyte proliferation, and results in anchorage-independent growth of melanocytes. Suppression of PHLPP1 involves blockade of binding of the transcription factor Sp1 to the PHLPP1 promoter. Collectively, these results suggest that suppression of PHLPP1 by DNA methylation contributes to melanoma development and progression.

Indexed as

Gene Expression Regulation, NeoplasticGene SilencingAnimalsCell Line, TumorCell ProliferationCell SurvivalDNA MethylationDown-RegulationEnzyme ActivationHumansMaleMelanomaMiceMice, NudeNuclear ProteinsPhosphatidylinositol 3-KinasesNuclear ProteinsPHLPP1 protein, humanPhosphatidylinositol 3-KinasesPhosphoprotein PhosphatasesProto-Oncogene Proteins c-aktSp1 Transcription Factor

Identifiers

PMID24121273
OpenAlexW2045993352

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.