Evidence map›Paper›PMID 27244599›Full record

ArticleScientific reports2016

Aerobic Exercise and Pharmacological Treatments Counteract Cachexia by Modulating Autophagy in Colon Cancer.

Eva Pigna, Emanuele Berardi, Paola Aulino, Emanuele Rizzuto, Sandra Zampieri, Ugo Carraro, Helmut Kern, Stefano Merigliano, Mario Gruppo, Mathias Mericskay and 8 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 123 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
123citing papers in PubMed, 1 pooled it
14.8field-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

123 citing papers in PubMed, 1 synthesis or guideline pooled it, 177 citations in OpenAlex.

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  13. Cancer Cachexia.Advances in experimental medicine and biology · 2025
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63 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

18 authors at 9 institutions in 4 countries.

Eva PignaDAHFMO Unit of Histology and Medical Embryology, Interuniversity Institute of Myology, Sapienza University of Rome, Italy.
Emanuele BerardiDAHFMO Unit of Histology and Medical Embryology, Interuniversity Institute of Myology, Sapienza University of Rome, Italy.
Paola AulinoDAHFMO Unit of Histology and Medical Embryology, Interuniversity Institute of Myology, Sapienza University of Rome, Italy.
Emanuele RizzutoDepartment of Mechanical &Aerospace Engineering, Sapienza University of Rome, Italy.
Sandra ZampieriDepartment of Biomedical Sciences, University of Padua, Italy.
Ugo CarraroIRCCS Fondazione Ospedale San Camillo, Venezia, Italy.
Helmut KernLudwig Boltzmann Institute of Electrical Stimulation and Physical Rehabilitation, Department of Physical Medicine and Rehabilitation, Wilhelminenspital Wien, Austria.
Stefano MeriglianoDepartment of Surgical and Gastroenterological Sciences, University of Padua, Italy.
Mario GruppoDepartment of Surgical and Gastroenterological Sciences, University of Padua, Italy.
Mathias MericskayDepartment of Biological Adaptation and Ageing B2A (CNRS UMR 8256 - INSERM ERL U1164 - UPMC P6), Pierre et Marie Curie University, Paris 6, France.
Zhenlin LiDepartment of Biological Adaptation and Ageing B2A (CNRS UMR 8256 - INSERM ERL U1164 - UPMC P6), Pierre et Marie Curie University, Paris 6, France.
Marco RocchiDepartment of Biomolecular Sciences, Unit of Biostatistics, "Carlo Bo" University of Urbino, Italy.
Rosario BaroneDepartment of Experimental Biomedicine and Clinical Neurosciences (BioNeC), University of Palermo, Italy.
Filippo MacalusoDepartment of Experimental Biomedicine and Clinical Neurosciences (BioNeC), University of Palermo, Italy.
Valentina Di FeliceDepartment of Experimental Biomedicine and Clinical Neurosciences (BioNeC), University of Palermo, Italy.
Sergio AdamoDAHFMO Unit of Histology and Medical Embryology, Interuniversity Institute of Myology, Sapienza University of Rome, Italy.
Dario ColettiDAHFMO Unit of Histology and Medical Embryology, Interuniversity Institute of Myology, Sapienza University of Rome, Italy.
Viviana MoresiDAHFMO Unit of Histology and Medical Embryology, Interuniversity Institute of Myology, Sapienza University of Rome, Italy.
Sapienza University of Rome · ITUniversity of Padua · ITUniversity of Palermo · ITCentre National de la Recherche Scientifique · FRAdaptation Biologique et VieillissementKU Leuven · BEOspedale generale di zona San Camillo Treviso · ITUniversity of Urbino · ITWilhelminen Hospital · AT

Funding

(PQD6) Muscle stem cells and cancer cachexiaR01CA180057 · NCI · OHIO STATE UNIVERSITY · PI GUTTRIDGE, DENIS C · 2013 to 2016
$1.5M
NCI NIH HHS R01 CA180057
6 · The paper itself

Abstract

Recent studies have correlated physical activity with a better prognosis in cachectic patients, although the underlying mechanisms are not yet understood. In order to identify the pathways involved in the physical activity-mediated rescue of skeletal muscle mass and function, we investigated the effects of voluntary exercise on cachexia in colon carcinoma (C26)-bearing mice. Voluntary exercise prevented loss of muscle mass and function, ultimately increasing survival of C26-bearing mice. We found that the autophagic flux is overloaded in skeletal muscle of both colon carcinoma murine models and patients, but not in running C26-bearing mice, thus suggesting that exercise may release the autophagic flux and ultimately rescue muscle homeostasis. Treatment of C26-bearing mice with either AICAR or rapamycin, two drugs that trigger the autophagic flux, also rescued muscle mass and prevented atrogene induction. Similar effects were reproduced on myotubes in vitro, which displayed atrophy following exposure to C26-conditioned medium, a phenomenon that was rescued by AICAR or rapamycin treatment and relies on autophagosome-lysosome fusion (inhibited by chloroquine). Since AICAR, rapamycin and exercise equally affect the autophagic system and counteract cachexia, we believe autophagy-triggering drugs may be exploited to treat cachexia in conditions in which exercise cannot be prescribed.

Indexed as

Physical Conditioning, AnimalAminoimidazole CarboxamideAnimalsAutophagosomesAutophagyCachexiaCell Line, TumorColonic NeoplasmsFemaleHumansLysosomesMiceMice, Inbred BALB CMuscle Fibers, SkeletalMuscle, SkeletalMuscle WeaknessAICA ribonucleotideAminoimidazole CarboxamideRibonucleotidesSirolimus

Identifiers

PMID27244599
PMCPMC4886631
OpenAlexW2408786519

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.