Evidence map›Paper›PMID 22334668›Full record

ArticleThe Journal of biological chemistry2012

Identification of Akt interaction protein PHF20/TZP that transcriptionally regulates p53.

Sungman Park, Donghwa Kim, Han C Dan, Huihua Chen, Joseph R Testa, Jin Q Cheng

RetractedOpen access · hybridAbstract readRetracted Publication
In one paragraph

Article in The Journal of biological chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. Targeting AKT for cancer therapy.Expert opinion on investigational drugs · 2019
    Review
  4. Article
  5. Adaptations to Endurance and Strength Training.Cold Spring Harbor perspectives in medicine · 2018
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Sungman ParkDepartment of Molecular Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida 33612, USA.
Donghwa Kim
Han C Dan
Huihua Chen
Joseph R Testa
Jin Q Cheng
Molecular Oncology (United States) · USMoffitt Cancer Center · USFox Chase Cancer Center · US

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI KENNETH Lynn WRIGHT · 1998 to 2026
$93.5M
Basis for Lymphomagenesis in Akt2 Transgenic MiceR01CA077429 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI TESTA, JOSEPH R. · 1998 to 2013
$4.7M
MicroRNAs in Human Ovarian CancerR01CA137041 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI CHENG, JIN Q · 2009 to 2013
$1.7M
NCI NIH HHS CA137041NCI NIH HHS CA77429NCI NIH HHS P30 CA076292NCI NIH HHS R01 CA077429NCI NIH HHS R01 CA137041
6 · The paper itself

Abstract

Akt regulates a diverse array of cellular functions, including cell survival, proliferation, differentiation, and metabolism. Although a number of molecules have been identified as upstream regulators and downstream targets of Akt, the mechanisms by which Akt regulates these cellular processes remain elusive. Here, we demonstrate that a novel transcription factor, PHF20/TZP (referring to Tudor and zinc finger domain containing protein), binds to Akt and induces p53 expression at the transcription level. Knockdown of PHF20 significantly reduces p53. PHF20 inhibits cell growth, DNA synthesis, and cell survival. Akt phosphorylates PHF20 at Ser(291) in vitro and in vivo, which results in its translocation from the nucleus to the cytoplasm and attenuation of PHF20 function. These data indicate that PHF20 is a substrate of Akt and plays a role in Akt cell survival/growth signaling.

Indexed as

Transcription, GeneticActive Transport, Cell NucleusAntigens, NeoplasmBiomarkers, TumorCell LineCell NucleusCell ProliferationCell SurvivalChromatinConsensus SequenceDNA-Binding ProteinsHumansNucleotide MotifsPhosphorylationProtein BindingProto-Oncogene Proteins c-aktAntigens, NeoplasmBiomarkers, TumorChromatinDNA-Binding ProteinsPHF20 protein, humanProto-Oncogene Proteins c-aktRNA, MessengerSerineTranscription FactorsTumor Suppressor Protein p53

Identifiers

PMID22334668
PMCPMC3322870
OpenAlexW1999853290

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.