Evidence map›Paper›PMID 29635516›Full record

ArticleHuman molecular genetics2018

Metabolomic studies identify changes in transmethylation and polyamine metabolism in a brain-specific mouse model of tuberous sclerosis complex.

James McKenna, David Kapfhamer, Jason M Kinchen, Brandi Wasek, Matthew Dunworth, Tracy Murray-Stewart, Teodoro Bottiglieri, Robert A Casero, Michael J Gambello

Open access · bronzeAbstract read
In one paragraph

Article in Human molecular genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

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  12. Polyamine Homeostasis in Snyder-Robinson Syndrome.Medical sciences (Basel, Switzerland) · 2018
    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

9 authors at 4 institutions in 1 country.

James McKennaDepartment of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA.
David KapfhamerDepartment of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA.
Jason M KinchenMetabolon, Inc., Durham, NC 27709, USA.
Brandi WasekCenter of Metabolomics, Baylor Scott and White Research Institute, Dallas 75204, TX, USA.
Matthew DunworthDepartment of Oncology, The Sidney Kimmel Comprehensive Cancer Center, The Johns Hopkins School of Medicine, Baltimore, MD 21231, USA.
Tracy Murray-StewartDepartment of Oncology, The Sidney Kimmel Comprehensive Cancer Center, The Johns Hopkins School of Medicine, Baltimore, MD 21231, USA.
Teodoro BottiglieriCenter of Metabolomics, Baylor Scott and White Research Institute, Dallas 75204, TX, USA.
Robert A CaseroDepartment of Oncology, The Sidney Kimmel Comprehensive Cancer Center, The Johns Hopkins School of Medicine, Baltimore, MD 21231, USA.
Michael J GambelloDepartment of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA.
Emory University · USSidney Kimmel Comprehensive Cancer Center · USBaylor Medical Center at Garland · USMetabolon (United States) · US

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI WILLIAM George NELSON · 1985 to 2026
$208.6M
Identification of novel spermine oxidase (SMOX) inhibitors as probes for an emerging chemoprevention targetR01CA204345 · NCI · JOHNS HOPKINS UNIVERSITY · PI CASERO, ROBERT A., WOSTER, PATRICK M · 2016 to 2020
$3.4M
The Role of Polyamines in the Neuropathology of Tuberous Sclerosis ComplexR21NS104410 · NINDS · EMORY UNIVERSITY · PI GAMBELLO, MICHAEL J · 2017 to 2018
$429k
NCI NIH HHS P30 CA006973NCI NIH HHS R01 CA204345NINDS NIH HHS R21 NS104410
6 · The paper itself

Abstract

Tuberous sclerosis complex (TSC) is an autosomal dominant neurodevelopmental disorder and the quintessential disorder of mechanistic Target of Rapamycin Complex 1 (mTORC1) dysregulation. Loss of either causative gene, TSC1 or TSC2, leads to constitutive mTORC1 kinase activation and a pathologically anabolic state of macromolecular biosynthesis. Little is known about the organ-specific metabolic reprogramming that occurs in TSC-affected organs. Using a mouse model of TSC in which Tsc2 is disrupted in radial glial precursors and their neuronal and glial descendants, we performed an unbiased metabolomic analysis of hippocampi to identify Tsc2-dependent metabolic changes. Significant metabolic reprogramming was found in well-established pathways associated with mTORC1 activation, including redox homeostasis, glutamine/tricarboxylic acid cycle, pentose and nucleotide metabolism. Changes in two novel pathways were identified: transmethylation and polyamine metabolism. Changes in transmethylation included reduced methionine, cystathionine, S-adenosylmethionine (SAM-the major methyl donor), reduced SAM/S-adenosylhomocysteine ratio (cellular methylation potential), and elevated betaine, an alternative methyl donor. These changes were associated with alterations in SAM-dependent methylation pathways and expression of the enzymes methionine adenosyltransferase 2A and cystathionine beta synthase. We also found increased levels of the polyamine putrescine due to increased activity of ornithine decarboxylase, the rate-determining enzyme in polyamine synthesis. Treatment of Tsc2+/- mice with the ornithine decarboxylase inhibitor α-difluoromethylornithine, to reduce putrescine synthesis dose-dependently reduced hippocampal astrogliosis. These data establish roles for SAM-dependent methylation reactions and polyamine metabolism in TSC neuropathology. Importantly, both pathways are amenable to nutritional or pharmacologic therapy.

Indexed as

MetabolomicsAnimalsBrainCystathionineCystathionine beta-SynthaseDisease Models, AnimalDNA MethylationEflornithineHumansMechanistic Target of Rapamycin Complex 1Methionine AdenosyltransferaseMiceNeuronsPolyaminesPutrescineS-AdenosylmethionineCystathionineCystathionine beta-SynthaseEflornithineMechanistic Target of Rapamycin Complex 1Methionine AdenosyltransferasePolyaminesPutrescineS-AdenosylmethionineTSC1 protein, humanTsc2 protein, mouseTuberous Sclerosis Complex 1 ProteinTuberous Sclerosis Complex 2 Protein

Identifiers

PMID29635516
PMCPMC5985733
OpenAlexW2796588110

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.