Evidence map›Paper›PMID 28483982›Full record

ArticleBiology open2017

Akt3 is responsible for the survival and proliferation of embryonic stem cells.

Ling Wang, Delun Huang, Zongliang Jiang, Yan Luo, Carol Norris, Ming Zhang, Xiuchun Tian, Young Tang

Open access · goldAbstract read
In one paragraph

Article in Biology open, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

21 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  11. Review
  12. CircMYC regulates the mitochondrial respiration and cell viabilityAmerican journal of translational research · 2021
    Article
  13. Article
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  15. International journal of molecular sciences · 2020
    Article
  16. Article
  17. Effects of high-fat diet and intestinal aryl hydrocarbon receptor deletion on colon carcinogenesis.American journal of physiology. Gastrointestinal and liver physiology · 2020
    Article
  18. Article
  19. Review
  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

8 authors at 2 institutions in 3 countries.

Ling WangDepartment of Animal Science, Institute for Systems Genomics, University of Connecticut, Storrs, CT 06269, USA.
Delun HuangDepartment of Animal Science, Institute for Systems Genomics, University of Connecticut, Storrs, CT 06269, USA.
Zongliang JiangDepartment of Animal Science, Institute for Systems Genomics, University of Connecticut, Storrs, CT 06269, USA.
Yan LuoDepartment of Animal Science, Institute for Systems Genomics, University of Connecticut, Storrs, CT 06269, USA.
Carol NorrisCenter for Open Research Resources and Equipment, University of Connecticut, Storrs, CT 06269, USA.
Ming ZhangAnimal Reproduction Institute, Guangxi University, Nanning, 530004, People's Republic of China.
Xiuchun TianDepartment of Animal Science, Institute for Systems Genomics, University of Connecticut, Storrs, CT 06269, USA xiuchun.tian@uconn.edu yong.tang@uconn.edu.
Young TangDepartment of Animal Science, Institute for Systems Genomics, University of Connecticut, Storrs, CT 06269, USA xiuchun.tian@uconn.edu yong.tang@uconn.edu.ORCID http://orcid.org/0000-0001-6188-7758
University of Connecticut · USGuangxi University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The phosphatidylinositol 3-kinase (PI3K)/protein kinase B (PKB/Akt) pathway plays an important role in regulating cell proliferation, metabolism, and survival. However, the distinct roles of Akt isoforms (Akt1, Akt2, and Akt3) in pluripotent stem cell maintenance are not fully defined. Using mouse embryonic stem cells (ESCs), we show that direct inhibition of Akt activity leads to ESC apoptosis. The Akt3, but not Akt1 or Akt2, activity specifically regulates this effect. Inhibiting Akt3 also leads to a cell cycle arrest at G1 phase. These regulatory roles of Akt3 are dependent on its kinase activity. Blocking the expression of Akt1 plus Akt2 in ESCs does not affect cell survival or proliferation, although blocking Akt1 aggravates the apoptotic effect induced by depletion of Akt3. We further show that blocking Akt3 in ESCs results in significant nuclear accumulation of p53, as well as the activation of its downstream targets, such as Mdm2, p21, and Fas. Inhibiting p53 and its downstream targets partially rescued the effects caused by Akt3-depletion. Our results revealed an Akt3 isoform-specific mechanism for ESC survival and proliferation involving the control of p53 activity.

Indexed as

Akt3Cell cycleCell survivalEmbryonic stem cellsp53

Identifiers

PMID28483982
PMCPMC5483023
OpenAlexW2612830819

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.