Evidence map›Paper›PMID 24084740›Full record

ArticleThe Journal of clinical investigation2013

NF-κB-mediated Pax7 dysregulation in the muscle microenvironment promotes cancer cachexia.

Wei A He, Emanuele Berardi, Veronica M Cardillo, Swarnali Acharyya, Paola Aulino, Jennifer Thomas-Ahner, Jingxin Wang, Mark Bloomston, Peter Muscarella, Peter Nau and 9 more

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 253 papers.

0numbers the graph read from it
0cells of the map it votes in
253citing papers in PubMed
14.2field-weighted citation impact, top 1% 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

253 citing papers in PubMed, 349 citations in OpenAlex.

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  10. The effects of tissue inflammation on cancer cachexia.Biochimica et biophysica acta. Molecular basis of disease · 2026
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193 more citing papers are in PubMed but not listed here.

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

19 authors at 7 institutions in 4 countries.

Wei A He
Emanuele Berardi
Veronica M Cardillo
Swarnali Acharyya
Paola Aulino
Jennifer Thomas-Ahner
Jingxin Wang
Mark Bloomston
Peter Muscarella
Peter Nau
Nilay Shah
Matthew E R Butchbach
Katherine Ladner
Sergio Adamo
Michael A Rudnicki
Charles Keller
Dario Coletti
Federica Montanaro
Denis C Guttridge
The Ohio State University · USNationwide Children's Hospital · USKU Leuven · BEMemorial Sloan Kettering Cancer Center · USOregon Health & Science University · USSorbonne Université · FRUniversity of Ottawa · CA

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
The Ohio State University Center for Clinical and Translational Science (UL1)UL1TR000090 · NCATS · OHIO STATE UNIVERSITY · PI JACKSON, REBECCA D · 2012 to 2013
$7.9M
Elucidating the role of NF-kB signaling in rhabdomyocarcomaR01CA143082 · NCI · OHIO STATE UNIVERSITY · PI GUTTRIDGE, DENIS C, KELLER, CHARLES · 2011 to 2015
$1.6M
(PQD6) Muscle stem cells and cancer cachexiaR01CA180057 · NCI · OHIO STATE UNIVERSITY · PI GUTTRIDGE, DENIS C · 2013 to 2016
$1.5M
NF-kB Regulation of Muscle Wasting in Cancer CachexiaR01CA098466 · NCI · OHIO STATE UNIVERSITY · PI GUTTRIDGE, DENIS C · 2003 to 2007
$1.2M
Cytokines and NFkappaBeta Regulation of Cancer CachexiaK01CA097953 · NCI · OHIO STATE UNIVERSITY · PI GUTTRIDGE, DENIS C · 2002 to 2006
$740k
Early Detection of Pancreatic Cancer CachexiaR03CA124692 · NCI · OHIO STATE UNIVERSITY · PI GUTTRIDGE, DENIS C · 2006 to 2007
$148k
NCATS NIH HHS UL1 TR000090NCATS NIH HHS UL1TR000090NCI NIH HHS K01 CA097953NCI NIH HHS K01CA097953NCI NIH HHS P30 CA016058NCI NIH HHS R01 CA098466NCI NIH HHS R01CA098466NCI NIH HHS R01 CA143082NCI NIH HHS R01 CA180057NCI NIH HHS R03 CA124692NCI NIH HHS R03CA124692
6 · The paper itself

Abstract

Cachexia is a debilitating condition characterized by extreme skeletal muscle wasting that contributes significantly to morbidity and mortality. Efforts to elucidate the underlying mechanisms of muscle loss have predominantly focused on events intrinsic to the myofiber. In contrast, less regard has been given to potential contributory factors outside the fiber within the muscle microenvironment. In tumor-bearing mice and patients with pancreatic cancer, we found that cachexia was associated with a type of muscle damage resulting in activation of both satellite and nonsatellite muscle progenitor cells. These muscle progenitors committed to a myogenic program, but were inhibited from completing differentiation by an event linked with persistent expression of the self-renewing factor Pax7. Overexpression of Pax7 was sufficient to induce atrophy in normal muscle, while under tumor conditions, the reduction of Pax7 or exogenous addition of its downstream target, MyoD, reversed wasting by restoring cell differentiation and fusion with injured fibers. Furthermore, Pax7 was induced by serum factors from cachectic mice and patients, in an NF-κB-dependent manner, both in vitro and in vivo. Together, these results suggest that Pax7 responds to NF-κB by impairing the regenerative capacity of myogenic cells in the muscle microenvironment to drive muscle wasting in cancer.

Indexed as

AdolescentAdultAgedAged, 80 and overAnimalsCachexiaCase-Control StudiesCell Line, TumorFemaleGene Expression Regulation, NeoplasticHumansMaleMiceMice, Inbred mdxMice, NudeMice, TransgenicNF-kappa BPAX7 protein, humanPax7 protein, mousePAX7 Transcription Factor

Identifiers

PMID24084740
PMCPMC3809785
OpenAlexW2147476151

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.