Evidence map›Paper›PMID 36461911›Full record

ArticleMolecular oncology2023

PP2A methylesterase PME-1 suppresses anoikis and is associated with therapy relapse of PTEN-deficient prostate cancers.

Anna Aakula, Aleksi Isomursu, Christian Rupp, Andrew Erickson, Nikhil Gupta, Otto Kauko, Pragya Shah, Artur Padzik, Yuba Raj Pokharel, Amanpreet Kaur and 9 more

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

6 citing papers in PubMed, 12 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

19 authors at 7 institutions in 4 countries.

Anna AakulaTurku Bioscience Centre, University of Turku and Åbo Akademi University, Finland.
Aleksi IsomursuTurku Bioscience Centre, University of Turku and Åbo Akademi University, Finland.
Christian RuppTurku Bioscience Centre, University of Turku and Åbo Akademi University, Finland.
Andrew EricksonHUSLAB Laboratory Services, Helsinki University Hospital Medicum and Institute for Molecular Medicine Finland FIMM, University of Helsinki, Finland.
Nikhil GuptaTurku Bioscience Centre, University of Turku and Åbo Akademi University, Finland.
Otto KaukoTurku Bioscience Centre, University of Turku and Åbo Akademi University, Finland.
Pragya ShahWeill Institute for Cell and Molecular Biology & Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA.
Artur PadzikTurku Bioscience Centre, University of Turku and Åbo Akademi University, Finland.
Yuba Raj PokharelTurku Bioscience Centre, University of Turku and Åbo Akademi University, Finland.
Amanpreet KaurTurku Bioscience Centre, University of Turku and Åbo Akademi University, Finland.
Song-Ping LiInstitute of Biomedicine, University of Turku, Finland.
Lloyd TrotmanCold Spring Harbor Laboratory, NY, USA.
Pekka TaimenInstitute of Biomedicine, University of Turku, Finland.
Antti RannikkoDepartment of Urology, Helsinki University Central Hospital, Finland.
Jan LammerdingWeill Institute for Cell and Molecular Biology & Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA.
Ilkka PaateroTurku Bioscience Centre, University of Turku and Åbo Akademi University, Finland.
Tuomas MirttiHUSLAB Laboratory Services, Helsinki University Hospital Medicum and Institute for Molecular Medicine Finland FIMM, University of Helsinki, Finland.
Johanna IvaskaTurku Bioscience Centre, University of Turku and Åbo Akademi University, Finland.ORCID https://orcid.org/0000-0002-6295-6556
Jukka WestermarckTurku Bioscience Centre, University of Turku and Åbo Akademi University, Finland.ORCID https://orcid.org/0000-0001-7478-3018
Åbo Akademi University · FICornell University · USUniversity of Helsinki · FICold Spring Harbor Laboratory · USHelsinki University Hospital · FIShenyang Pharmaceutical University · CNUniversity of Turku · FI

Funding

Project 3: Physical and Metabolic Constraints of Cancer Cell InvasionU54CA210184 · NCI · CORNELL UNIVERSITY · PI ZIPFEL, WARREN R · 2016 to 2020
$10.2M
Nuclear mechanics and mechanotransduction in muscular laminopathiesR01HL082792 · NHLBI · CORNELL UNIVERSITY · PI LAMMERDING, JAN · 2007 to 2023
$4.8M
Metastasis of PTEN Mutant Prostate CancerR01CA275128 · NCI · COLD SPRING HARBOR LABORATORY · PI TROTMAN, LLOYD C · 2022 to 2025
$2.7M
Nuclear mechanobiology in confined migration (Equipment Supplement 2023)R01GM137605 · NIGMS · CORNELL UNIVERSITY · PI LAMMERDING, JAN · 2020 to 2023
$1.6M
NCI NIH HHS R01 CA275128NCI NIH HHS U54 CA210184NHLBI NIH HHS R01 HL082792NIGMS NIH HHS R01 GM137605NIH HHS R01 GM137605NIH HHS R01HL082792NIH HHS U54CA210184
6 · The paper itself

Abstract

While organ-confined prostate cancer (PCa) is mostly therapeutically manageable, metastatic progression of PCa remains an unmet clinical challenge. Resistance to anoikis, a form of cell death initiated by cell detachment from the surrounding extracellular matrix, is one of the cellular processes critical for PCa progression towards aggressive disease. Therefore, further understanding of anoikis regulation in PCa might provide therapeutic opportunities. Here, we discover that PCa tumours with concomitant inhibition of two tumour suppressor phosphatases, PP2A and PTEN, are particularly aggressive, having < 50% 5-year secondary-therapy-free patient survival. Functionally, overexpression of PME-1, a methylesterase for the catalytic PP2A-C subunit, inhibits anoikis in PTEN-deficient PCa cells. In vivo, PME-1 inhibition increased apoptosis in in ovo PCa tumour xenografts, and attenuated PCa cell survival in zebrafish circulation. Molecularly, PME-1-deficient PC3 cells display increased trimethylation at lysines 9 and 27 of histone H3 (H3K9me3 and H3K27me3), a phenotype known to correlate with increased apoptosis sensitivity. In summary, our results demonstrate that PME-1 supports anoikis resistance in PTEN-deficient PCa cells. Clinically, these results identify PME-1 as a candidate biomarker for a subset of particularly aggressive PTEN-deficient PCa.

Indexed as

AnoikisCarboxylic Ester HydrolasesProstatic NeoplasmsAnimalsHumansMaleNeoplasm Recurrence, LocalPTEN PhosphohydrolaseZebrafishCarboxylic Ester Hydrolasesprotein phosphatase methylesterase-1PTEN PhosphohydrolasePTEN protein, humananoikisintegrinLAP2A/Bnuclear laminaPP2A-C methylationPPME1

Identifiers

PMID36461911
PMCPMC10257411
OpenAlexW4310642170

What OpenQuestion holds

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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.