Evidence map›Paper›PMID 21948699›Full record

ArticleStem cells (Dayton, Ohio)2011

Phosphatase and tensin homolog regulates the pluripotent state and lineage fate choice in human embryonic stem cells.

Jackelyn A Alva, Grace E Lee, Erika E Escobar, April D Pyle

Open access · bronzeAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

19 citing papers in PubMed, 43 citations in OpenAlex.

  1. Chicken Primordial Germ Cells Do Not Proliferate in Insulin-Lacking Media.International journal of molecular sciences · 2025
    Article
  2. Review
  3. Review
  4. Derivation of induced pluripotent stem cells from ferret somatic cells.American journal of physiology. Lung cellular and molecular physiology · 2020
    Article
  5. PI3K in stemness regulation: from development to cancer.Biochemical Society transactions · 2020
    Review
  6. Article
  7. Article
  8. OncogenicProceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  9. PTEN Inhibition in Human Disease Therapy.Molecules (Basel, Switzerland) · 2018
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Testicular cancer: biology and biomarkers.Virchows Archiv : an international journal of pathology · 2014
    Review
  16. Review
  17. Review
  18. Inhibition of PTEN tumor suppressor promotes the generation of induced pluripotent stem cells.Molecular therapy : the journal of the American Society of Gene Therapy · 2013
    Article
  19. 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

4 authors at 2 institutions in 1 country.

Jackelyn A AlvaDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, California 90095, USA.
Grace E Lee
Erika E Escobar
April D Pyle
University of California, Los Angeles · USBroad Center · US

Funding

UCLA Tumor Immunology Training ProgramT32CA009120 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Steven M. Dubinett, MICHAEL A TEITELL · 1985 to 2026
$10.3M
MARC U*STAR Program at the University of California, Los AngelesT34GM008563 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MCEVOY, MEGAN M, POE, GINA R · 1996 to 2023
$9.7M
NCI NIH HHS T32 CA009120NCI NIH HHS T32CA009120-33
6 · The paper itself

Abstract

Understanding the intrinsic and extrinsic signals that regulate the molecular basis of the pluripotent state may improve our understanding of mammalian embryogenesis, different states of pluripotency, and our ability to tailor lineage differentiation. Although the role of the PI3K/Akt pathway in the self-renewal and maintenance of mESCs is well-established, the specific contribution of the pathway or of its negative regulator, PTEN, in the maintenance of the human pluripotent state is less understood. To explore the PI3K/AKT pathway in human embryonic stem cell (hESC) pluripotency and differentiation, we generated stable PTEN knockdown (KD) hESCs using short hairpin RNA. Similar to mESCs, we found that PTEN KD hESCs have increased self-renewal, cell survival, and proliferation over multiple passages compared to control cells. However, in contrast to mESCs, in vitro, PTEN KD hESCs differentiated inefficiently in directed differentiation assays, in part due to the continued maintenance of OCT4 and NANOG expression. In teratoma assays, PTEN KD hESCs generated tissues from the three germ layers, although with a bias toward neuroectoderm differentiation. These results demonstrate that PTEN is a key regulator of hESC growth and differentiation, and manipulation of this pathway may improve our ability to regulate and understand the pluripotent state.

Indexed as

Cell DifferentiationAnimalsCell LineCell LineageCell ProliferationCell SurvivalEmbryonic Stem CellsGene Knockdown TechniquesHomeodomain ProteinsHumansLentivirusMaleMiceMice, SCIDNanog Homeobox ProteinOctamer Transcription Factor-3Homeodomain ProteinsNanog Homeobox ProteinNANOG protein, humanOctamer Transcription Factor-3Phosphatidylinositol 3-KinasesPOU5F1 protein, humanPTEN PhosphohydrolasePTEN protein, humanRNA, Small Interfering

Identifiers

PMID21948699
PMCPMC3898662
OpenAlexW2080580581

What OpenQuestion holds

Textmetadata
LicenceTDM
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.