Evidence map›Paper›PMID 33503847›Full record

ArticleBiomolecules2021

Efficacy of Providing the PI3K p110α Inhibitor BYL719 (Alpelisib) to Middle-Aged Mice in Their Diet.

Christopher P Hedges, Jordi Boix, Jagdish K Jaiswal, Bhoopika Shetty, Peter R Shepherd, Troy L Merry

Open access · goldAbstract read
In one paragraph

Article in Biomolecules, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

7 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. PI3K inhibitors are finally coming of age.Nature reviews. Drug discovery · 2021
    Review
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

6 authors at 1 institution in 1 country.

Christopher P HedgesDiscipline of Nutrition, School of Medical Sciences, University of Auckland, Auckland 1023, New Zealand.ORCID 0000-0003-1104-0385
Jordi BoixCentre for Brain Research, University of Auckland, Auckland 1023, New Zealand.ORCID 0000-0001-8460-2567
Jagdish K JaiswalMaurice Wilkins Centre for Molecular Biodiscovery, University of Auckland, Auckland 1023, New Zealand.ORCID 0000-0002-0731-2117
Bhoopika ShettyDiscipline of Nutrition, School of Medical Sciences, University of Auckland, Auckland 1023, New Zealand.ORCID 0000-0002-0221-2483
Peter R ShepherdMaurice Wilkins Centre for Molecular Biodiscovery, University of Auckland, Auckland 1023, New Zealand.
Troy L MerryDiscipline of Nutrition, School of Medical Sciences, University of Auckland, Auckland 1023, New Zealand.
University of Auckland · NZ

Funding

Health Research Council of New Zealand 17/099Rutherford Discovery Fellowship RDF-15-UOA-020
6 · The paper itself

Abstract

BYL719 (alpelisib) is a small molecule inhibitor of PI3K p110α developed for cancer therapy. Targeted suppression of PI3K has led to lifespan extension in rodents and model organisms. If PI3K inhibitors are to be considered as an aging therapeutic, it is important to understand the potential consequences of long-term exposure, and the most practical way to achieve this is through diet administration. Here, we investigated the pharmacokinetics of BYL719 delivered in diet and the efficacy of BYL719 to suppress insulin signaling when administered in the diet of 8-month-old male and female mice. Compared to oral gavage, diet incorporation resulted in a lower peak plasma BYL719 (3.6 vs. 9.2 μM) concentration but similar half-life (~1.5 h). Consuming BYL719 resulted in decreased insulin signaling in liver and muscle within 72 h, and mice still showed impaired glucose tolerance and insulin sensitivity following 6 weeks of access to a diet containing 0.3 g/kg BYL719. However, consuming BYL719 did not affect food intake, body mass, muscle function (rotarod and hang time performance) or cognitive behaviors. This provides evidence that BYL719 has long-term efficacy without major toxicity or side effects, and suggests that administering BYL719 in diet is suitable for studying the effect of pharmacological suppression of PI3K p110α on aging and metabolic function.

Indexed as

AgingAnimalsBehavior, AnimalClass I Phosphatidylinositol 3-KinasesFemaleGlucoseGlucose Tolerance TestHomeostasisLiverMaleMiceMice, Inbred C57BLMusclesMuscle, SkeletalPhosphatidylinositol 3-KinasesReceptor, Insulin1-phosphatidylinositol 3-kinase p110 subunit, mouseAlpelisibClass I Phosphatidylinositol 3-KinasesGlucosePhosphatidylinositol 3-KinasesReceptor, InsulinThiazolesagingBYL-719glucose toleranceinsulin signalingpharmacokinetics

Identifiers

PMID33503847
PMCPMC7911305
OpenAlexW3124080678

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.