Evidence mapPaperPMID 36232456Full record

ArticleInternational journal of molecular sciences2022

Heterozygous Loss of KRIT1 in Mice Affects Metabolic Functions of the Liver, Promoting Hepatic Oxidative and Glycative Stress.

Raffaella Mastrocola, Eleonora Aimaretti, Gustavo Ferreira Alves, Alessia Sofia Cento, Claudia Fornelli, Federica Dal Bello, Chiara Ferraris, Luca Goitre, Andrea Perrelli, Saverio Francesco Retta

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. KRIT1 in vascular biology and beyond.Bioscience reports · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. 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

10 authors at 3 institutions in 3 countries.

Raffaella MastrocolaDepartment of Clinical and Biological Sciences, University of Torino, 10043 Orbassano (TO), Italy.ORCID 0000-0002-0104-6129
Eleonora AimarettiDepartment of Clinical and Biological Sciences, University of Torino, 10043 Orbassano (TO), Italy.ORCID 0000-0001-6336-1442
Gustavo Ferreira AlvesDepartment of Neurosciences "Rita Levi Montalcini", University of Torino, 10126 Torino (TO), Italy.ORCID 0000-0003-2529-2006
Alessia Sofia CentoDepartment of Clinical and Biological Sciences, University of Torino, 10043 Orbassano (TO), Italy.
Claudia FornelliDepartment of Clinical and Biological Sciences, University of Torino, 10043 Orbassano (TO), Italy.
Federica Dal BelloDepartment of Molecular Biotechnology and Health Sciences, University of Torino, 10126 Torino (TO), Italy.ORCID 0000-0003-0726-3025
Chiara FerrarisDepartment of Clinical and Biological Sciences, University of Torino, 10043 Orbassano (TO), Italy.
Luca GoitreDepartment of Clinical and Biological Sciences, University of Torino, 10043 Orbassano (TO), Italy.
Andrea PerrelliDepartment of Clinical and Biological Sciences, University of Torino, 10043 Orbassano (TO), Italy.ORCID 0000-0001-8512-6080
Saverio Francesco RettaDepartment of Clinical and Biological Sciences, University of Torino, 10043 Orbassano (TO), Italy.ORCID 0000-0001-9761-2959
University of Turin · ITUniversidade Federal de Santa Catarina · BRUniversity of Rochester Medical Center · US

Funding

Fondazione CRT Cerebro-NGS.TOTelethon Foundation GGP15219University of Turin Local Research Funding 2018-21
6 · The paper itself

Abstract

KRIT1 loss-of-function mutations underlie the pathogenesis of Cerebral Cavernous Malformation (CCM), a major vascular disease affecting the central nervous system (CNS). However, KRIT1 is also expressed outside the CNS and modulates key regulators of metabolic and oxy-inflammatory pathways, including the master transcription factor FoxO1, suggesting a widespread functional significance. Herein, we show that the KRIT1/FoxO1 axis is implicated in liver metabolic functions and antioxidative/antiglycative defenses. Indeed, by performing comparative studies in KRIT1 heterozygous (KRIT1

Indexed as

InsulinsNF-E2-Related Factor 2AnimalsAntioxidantsGlucoseGlycogenKRIT1 ProteinLiverMiceOxidative StressAntioxidantsGlucoseGlycogenInsulinsKRIT1 ProteinKrit1 protein, mouseNF-E2-Related Factor 2adaptive redox and metabolic homeostasisadvanced glycation end-products (AGEs)FoxO1hepatic antioxidant and antiglycative defenseshepatic glucose metabolismhepatic insulin signalingKRIT1/CCM1Nrf2redox-metabolic interplay

Identifiers

PMID36232456
PMCPMC9570113
OpenAlexW4296993374

What Socratic 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 Socratic graph.