Evidence map›Paper›PMID 22473468›Full record

ReviewNature reviews. Molecular cell biology2012

The functions and regulation of the PTEN tumour suppressor.

Min Sup Song, Leonardo Salmena, Pier Paolo Pandolfi

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Molecular cell biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1,136 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1,136citing papers in PubMed, 2 pooled it
73.3field-weighted citation impact, top 1% 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

1,136 citing papers in PubMed, 2 syntheses or guidelines pooled it, 1,905 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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    Review
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  9. Review
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  12. Article
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  15. SurvGRN: a multi-feature fusion framework for bladder cancer survival prediction.International journal of surgery (London, England) · 2026
    Article
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  19. Development of aBioactive materials · 2026
    Article
  20. Article

1,076 more citing papers are in PubMed but not listed here.

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

3 authors at 3 institutions in 2 countries.

Min Sup SongCancer Genetics Program, Beth Israel Deaconess Cancer Center, Department of Medicine and Pathology, Harvard Medical School, Boston, Massachuchetts 02215, USA. msong@bidmc.harvard.edu
Leonardo Salmena
Pier Paolo Pandolfi
Beth Israel Deaconess Medical Center · USHarvard University Press · USPrincess Margaret Cancer Centre · CA

Funding

Canadian Institutes of Health ResearchNCI NIH HHS R01 CA‑82328‑09
6 · The paper itself

Abstract

The importance of the physiological function of phosphatase and tensin homologue (PTEN) is illustrated by its frequent disruption in cancer. By suppressing the phosphoinositide 3-kinase (PI3K)-AKT-mammalian target of rapamycin (mTOR) pathway through its lipid phosphatase activity, PTEN governs a plethora of cellular processes including survival, proliferation, energy metabolism and cellular architecture. Consequently, mechanisms regulating PTEN expression and function, including transcriptional regulation, post-transcriptional regulation by non-coding RNAs, post-translational modifications and protein-protein interactions, are all altered in cancer. The repertoire of PTEN functions has recently been expanded to include phosphatase-independent activities and crucial functions within the nucleus. Our increasing knowledge of PTEN and pathologies in which its function is altered will undoubtedly inform the rational design of novel therapies.

Indexed as

Gene Expression RegulationAnimalsCell NucleusHumansMutationNeoplasmsNeoplastic Stem CellsProtein ConformationPTEN PhosphohydrolaseSignal TransductionTumor Suppressor ProteinsPTEN PhosphohydrolasePTEN protein, humanTumor Suppressor Proteins

Identifiers

PMID22473468
OpenAlexW2017739035

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.