Evidence map›Paper›PMID 25116380›Full record

ArticleCancer medicine2014

Acetylation-dependent regulation of essential iPS-inducing factors: a regulatory crossroad for pluripotency and tumorigenesis.

Xiangpeng Dai, Pengda Liu, Alan W Lau, Yueyong Liu, Hiroyuki Inuzuka

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Xiangpeng DaiDepartment of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.
Pengda Liu
Alan W Lau
Yueyong Liu
Hiroyuki Inuzuka
Beth Israel Deaconess Medical Center · USHarvard University · US

Funding

Training Program in Angiogenesis &InflammationT32HL007893 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI DVORAK, HAROLD FISHER · 1998 to 2017
$5.5M
New insights into the role of the Fbw7 tumor suppressor in senescence and agingK01AG041218 · NIA · BETH ISRAEL DEACONESS MEDICAL CENTER · PI INUZUKA, HIROYUKI · 2011 to 2015
$621k
Elucidating a Novel Akt Activation Mechanism for Targeted Prostate Cancer TherapyK99CA181342 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI LIU, PENGDA · 2014 to 2015
$339k
NCI NIH HHS K99 CA181342NHLBI NIH HHS 5T32HL007893NHLBI NIH HHS T32 HL007893NIA NIH HHS AG041218NIA NIH HHS K01 AG041218
6 · The paper itself

Abstract

Induced pluripotent stem (iPS) cells can be generated from somatic cells by coexpression of four transcription factors: Sox2, Oct4, Klf4, and c-Myc. However, the low efficiency in generating iPS cells and the tendency of tumorigenesis hinder the therapeutic applications for iPS cells in treatment of human diseases. To this end, it remains largely unknown how the iPS process is subjected to regulation by upstream signaling pathway(s). Here, we report that Akt regulates the iPS process by modulating posttranslational modifications of these iPS factors in both direct and indirect manners. Specifically, Akt directly phosphorylates Oct4 to modulate the Oct4/Sox2 heterodimer formation. Furthermore, Akt either facilitates the p300-mediated acetylation of Oct4, Sox2, and Klf4, or stabilizes Klf4 by inactivating GSK3, thus indirectly modulating stemness. As tumorigenesis shares possible common features and mechanisms with iPS, our study suggests that Akt inhibition might serve as a cancer therapeutic approach to target cancer stem cells.

Indexed as

Cellular ReprogrammingAmino Acid MotifsAmino Acid SequenceCell Cycle ProteinsCell LineCell Transformation, NeoplasticE1A-Associated p300 ProteinF-Box ProteinsF-Box-WD Repeat-Containing Protein 7Gene Expression RegulationGlycogen Synthase Kinase 3HumansInduced Pluripotent Stem CellsKruppel-Like Factor 4Kruppel-Like Transcription FactorsModels, BiologicalacetylacetoneCell Cycle ProteinsE1A-Associated p300 ProteinF-Box ProteinsF-Box-WD Repeat-Containing Protein 7FBXW7 protein, humanGlycogen Synthase Kinase 3KLF4 protein, humanKruppel-Like Factor 4Kruppel-Like Transcription FactorsOctamer Transcription Factor-3PentanonesProto-Oncogene Proteins c-aktSOXB1 Transcription FactorsUbiquitin-Protein LigasesAktiPS cellKlf4Oct4p300Sox2

Identifiers

PMID25116380
PMCPMC4302671
OpenAlexW2149829585

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.