Evidence map›Paper›PMID 23832960›Full record

ArticleEndocrinology2013

Inhibition of cisplatin-induced lipid catabolism and weight loss by ghrelin in male mice.

Jose M Garcia, Thomas Scherer, Ji-an Chen, Bobby Guillory, Anriada Nassif, Victor Papusha, Joanna Smiechowska, Mark Asnicar, Christoph Buettner, Roy G Smith

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

60 citing papers in PubMed, 119 citations in OpenAlex.

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  11. Exercise alleviates cisplatin-induced toxicity in the hippocampus of mice by inhibiting neuroinflammation and improving synaptic plasticity.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2024
    Article
  12. Drug-related sarcopenia as a secondary sarcopenia.Geriatrics & gerontology international · 2024
    Review
  13. Article
  14. Review
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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

10 authors at 4 institutions in 1 country.

Jose M GarciaDepartment of Medicine and Molecular and Cell Biology, Baylor College of Medicine, Houston, Texas 77030, USA. jgarcia1@bcm.edu
Thomas Scherer
Ji-an Chen
Bobby Guillory
Anriada Nassif
Victor Papusha
Joanna Smiechowska
Mark Asnicar
Christoph Buettner
Roy G Smith
Baylor College of Medicine · USMichael E. DeBakey VA Medical Center · USIcahn School of Medicine at Mount Sinai · USUniversity of Pittsburgh · US

Funding

VESICULAR LOCALIZATION AND FUNCTION OF PRESENILIN 1 FRAGMENTP50AG005138 · NIA · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI NEUGROSCHL, JUDITH · 1985 to 2019
$37.9M
Vanderbilt Diabetes Research CenterP30DK020593 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI OWEN P MCGUINNESS · 2012 to 2026
$29.3M
TRANSGENIC MOUSE/ ES CELL SHARES RESOURCESP60DK020593 · NIDDK · VANDERBILT UNIVERSITY · PI MCGUINNESS, OWEN P · 1986 to 2011
$28.1M
Vanderbilt Mouse Metabolic Physiology CenterU24DK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2001 to 2015
$14.9M
Diabetes Endocrinology Research CenterP30DK079638 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI CHAN, LAWRENCE · 2008 to 2012
$6.4M
Vanderbilt Mouse Metabolic Phenotyping CenterU2CDK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2016 to 2021
$6.3M
CELL &MOLECULAR BIOLOGY OF AGINGT32AG000183 · NIA · BAYLOR COLLEGE OF MEDICINE · PI DONEHOWER, LAWRENCE A. · 1989 to 2015
$3.7M
Ghrelin Regulation: Implications for Understanding ObesityR01DK076037 · NIDDK · UNIVERSITY OF VIRGINIA · PI THORNER, MICHAEL O · 2008 to 2012
$2.7M
Regulation of Adipose Tissue Metabolism by Central Insulin and LeptinR01DK083658 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BUETTNER, CHRISTOPH · 2009 to 2013
$1.9M
Training in Renal, GI, Endocrine, and Epithelial BiologyT35DK065521 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DEFRANCO, DONALD B, JURCZAK, MICHAEL J. · 2004 to 2024
$811k
The role of the endocannabinoid system in regulating hepatic glucose fluxesR03DK082724 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BUETTNER, CHRISTOPH · 2009 to 2010
$169k
The role of ghrelin and the ghrelin receptor GHSR1a in sarcopenia of agingR03AG040583 · NIA · BAYLOR COLLEGE OF MEDICINE · PI GARCIA, JOSE M. · 2011 to 2012
$157k
BLRD VA I01 BX000507CSRD VA I01 CX000174NIA NIH HHS AG040583NIA NIH HHS P50 AG005138NIA NIH HHS R03 AG040583NIA NIH HHS T32 AG000183NIA NIH HHS T32AG000183NIDDK NIH HHS DK020593NIDDK NIH HHS DK059637NIDDK NIH HHS DK 065521NIDDK NIH HHS DK076037NIDDK NIH HHS DK082724NIDDK NIH HHS DK083658NIDDK NIH HHS P30 DK020593NIDDK NIH HHS P30 DK079638NIDDK NIH HHS P60 DK020593NIDDK NIH HHS R01 DK076037NIDDK NIH HHS R01 DK083658NIDDK NIH HHS R03 DK082724NIDDK NIH HHS R56 DK083658NIDDK NIH HHS T35 DK065521NIDDK NIH HHS U24 DK059637NIDDK NIH HHS U24 DK59637
6 · The paper itself

Abstract

Cachexia, defined as an involuntary weight loss ≥ 5%, is a serious and dose-limiting side effect of chemotherapy that decreases survival in cancer patients. Alterations in lipid metabolism are thought to cause the lipodystrophy commonly associated with cachexia. Ghrelin has been proposed to ameliorate the alterations in lipid metabolism due to its orexigenic and anabolic properties. However, the mechanisms of action through which ghrelin could potentially ameliorate chemotherapy-associated cachexia have not been elucidated. The objectives of this study were to identify mechanisms by which the chemotherapeutic agent cisplatin alters lipid metabolism and to establish the role of ghrelin in reversing cachexia. Cisplatin-induced weight and fat loss were prevented by ghrelin. Cisplatin increased markers of lipolysis in white adipose tissue (WAT) and of β-oxidation in liver and WAT and suppressed lipogenesis in liver, WAT, and muscle. Ghrelin prevented the imbalance between lipolysis, β-oxidation, and lipogenesis in WAT and muscle. Pair-feeding experiments demonstrated that the effects of cisplatin and ghrelin on lipogenesis, but not on lipolysis and β-oxidation, were due to a reduction in food intake. Thus, ghrelin prevents cisplatin-induced weight and fat loss by restoring adipose tissue functionality. An increase in caloric intake further enhances the anabolic effects of ghrelin.

Indexed as

Adipose Tissue, WhiteAdiposityAnimalsAntineoplastic AgentsAppetite StimulantsBiomarkersCachexiaCisplatinEnergy IntakeGene Expression Regulation, EnzymologicGhrelinLipogenesisLipolysisLiverMaleMiceAntineoplastic AgentsAppetite StimulantsBiomarkersCisplatinGhrelin

Identifiers

PMID23832960
PMCPMC3749475
OpenAlexW1990433760

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.