Evidence map›Paper›PMID 23056600›Full record

ArticlePloS one2012

Cthrc1, a novel circulating hormone regulating metabolism.

J Patrizia Stohn, Nicole G Perreault, Qiaozeng Wang, Lucy Liaw, Volkhard Lindner

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

33 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
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  10. Tranexamic acid reduces inflammation, edema and burn wound conversion in a rodent model.Burns : journal of the International Society for Burn Injuries · 2024
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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

5 authors at 1 institution in 1 country.

J Patrizia StohnCenter for Molecular Medicine, Maine Medical Center Research Institute, Scarborough, Maine, United States of America.
Nicole G Perreault
Qiaozeng Wang
Lucy Liaw
Volkhard Lindner
Maine Medical Center Research Institute · US

Funding

Transcriptional Decisions in Endothelial Cell DifferentiationP20RR015555 · NCRR · MAINE MEDICAL CENTER · PI PRUDOVSKY, IGOR · 2000 to 2009
$21.4M
WNT SIGNALING IN PREIMPLANTATION EMBRYOP20RR018789 · NCRR · MAINE MEDICAL CENTER · PI WANG, ZACK Z. · 2003 to 2011
$18.9M
Phase III COBRE in Vascular BiologyP30GM103392 · NIGMS · MAINEHEALTH · PI ST. GERMAIN, DONALD L. · 2012 to 2016
$4.7M
Remodelin, a Novel Vascular Injury and Bone Related GeneR01HL069182 · NHLBI · MAINE MEDICAL CENTER · PI LINDNER, VOLKHARD · 2002 to 2013
$3.5M
COBRE in Stem Cell Biology and Regenerative MedicineP20GM103465 · NIGMS · MAINEHEALTH · PI WOJCHOWSKI, DON MICHAEL · 2012 to 2012
$2.0M
PHASE III COBRE IN VASCULAR BIOLOGYP30RR030927 · NCRR · MAINEHEALTH · PI FRIESEL, ROBERT E · 2011 to 2011
$1.2M
NCRR NIH HHS P20 RR015555NCRR NIH HHS P20 RR018789NCRR NIH HHS P20RR018789NCRR NIH HHS P20 RR-15555NCRR NIH HHS P30 RR030927NCRR NIH HHS P30RR030927NHLBI NIH HHS HL69182NHLBI NIH HHS R01 HL069182NIGMS NIH HHS P20 GM103465NIGMS NIH HHS P20GM103465NIGMS NIH HHS P30 GM103392NIGMS NIH HHS P30GM103392
6 · The paper itself

Abstract

backgroundWe discovered the gene Collagen Triple Helix Repeat Containing 1 (Cthrc1) and reported its developmental expression and induction in adventitial cells of injured arteries and dermal cells of skin wounds. The role of Cthrc1 in normal adult tissues has not yet been determined. METHODOLOGY/PRINCIPAL

findingsWe generated mutant mice with a novel Cthrc1 null allele by homologues recombination. Cthrc1 null mice appeared developmentally normal. On the C57BL/6J background, livers from Cthrc1 null mice accumulated vast quantities of lipid, leading to extensive macrovesicular steatosis. Glycogen levels in skeletal muscle and liver of Cthrc1 null mice on the 129S6/SvEv background were significantly increased. However, Cthrc1 expression is not detectable in these tissues in wild-type mice, suggesting that the lipid and glycogen storage phenotype may be a secondary effect due to loss of Cthrc1 production at a distant site. To investigate potential hormonal functions of Cthrc1, tissues from adult mice and pigs were examined for Cthrc1 expression by immunohistochemistry with monoclonal anti-Cthrc1 antibodies. In pigs, Cthrc1 was detected around chromophobe cells of the anterior pituitary, and storage of Cthrc1 was observed in colloid-filled follicles and the pituitary cleft. Pituitary follicles have been observed in numerous vertebrates including humans but none of the known pituitary hormones have hitherto been detected in them. In C57BL/6J mice, however, Cthrc1 was predominantly expressed in the paraventricular and supraoptic nucleus of the hypothalamus but not in the posterior pituitary. In human plasma, we detected Cthrc1 in pg/ml quantities and studies with (125)I-labeled Cthrc1 revealed a half-life of 2.5 hours in circulation. The highest level of Cthrc1 binding was observed in the liver.

conclusionsCthrc1 has characteristics of a circulating hormone generated from the anterior pituitary, hypothalamus and bone. Hormonal functions of Cthrc1 include regulation of lipid storage and cellular glycogen levels with potentially broad implications for cell metabolism and physiology.

Indexed as

AnimalsExtracellular Matrix ProteinsGlycogenGlycoproteinsImmunohistochemistryLipid MetabolismLiverMaleMiceMice, KnockoutRatsRats, Sprague-DawleyCthrc1 protein, mouseCthrc1 protein, ratExtracellular Matrix ProteinsGlycogenGlycoproteins

Identifiers

PMID23056600
PMCPMC3466254
OpenAlexW1979704727

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.