Evidence map›Paper›PMID 33177579›Full record

ArticleScientific reports2020

Chemoradiation impairs myofiber hypertrophic growth in a pediatric tumor model.

Nicole D Paris, Jacob G Kallenbach, John F Bachman, Roméo S Blanc, Carl J Johnston, Eric Hernady, Jacqueline P Williams, Joe V Chakkalakal

Abstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

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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

8 authors.

Nicole D ParisDepartment of Pharmacology and Physiology, University of Rochester Medical Center, Rochester, NY, USA.
Jacob G KallenbachDepartment of Pharmacology and Physiology, University of Rochester Medical Center, Rochester, NY, USA.
John F BachmanDepartment of Pharmacology and Physiology, University of Rochester Medical Center, Rochester, NY, USA.
Roméo S BlancDepartment of Pharmacology and Physiology, University of Rochester Medical Center, Rochester, NY, USA.
Carl J JohnstonDepartment of Pediatrics, University of Rochester Medical Center, Rochester, NY, USA.
Eric HernadyDepartment of Radiation Oncology, University of Rochester Medical Center, Rochester, NY, USA.
Jacqueline P WilliamsWilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, USA.
Joe V ChakkalakalDepartment of Pharmacology and Physiology, University of Rochester Medical Center, Rochester, NY, USA. joe_chakkalakal@urmc.rochester.edu.

Funding

Rochester Resource-Based Center for Bone, Muscle and Orthopaedic Research (ROCSTARR) (Overall Application)P30AR069655 · NIAMS · UNIVERSITY OF ROCHESTER · PI Edward M. Schwarz · 2016 to 2026
$7.8M
Training in Orthopaedic Researchhttps://apps.era.nih.gov/grantfolder/viewInternalGF.era?applId=8841318&folderId=90T32AR053459 · NIAMS · UNIVERSITY OF ROCHESTER · PI ZUSCIK, MICHAEL J · 2006 to 2017
$3.4M
Interrelationships between age-related skeletal muscle stem cell and NMJ declineR01AG051456 · NIA · UNIVERSITY OF ROCHESTER · PI CHAKKALAKAL, JOE · 2015 to 2019
$1.9M
Cellular Basis for Radiation induced acceleration of sarcopenia in juvenile cancer survivorsR01CA220467 · NCI · UNIVERSITY OF ROCHESTER · PI CHAKKALAKAL, JOE · 2017 to 2021
$1.8M
SARRP 200 Platform for Image Guided Micro IrradiationS10OD021548 · OD · UNIVERSITY OF ROCHESTER · PI WILLIAMS, JACQUELINE PATRICIA · 2016 to 2016
$600k
NCI NIH HHS R01 CA220467NCI NIH HHS R01CA220467NIAMS NIH HHS P30 AR069655NIAMS NIH HHS T32 AR053459NIA NIH HHS R01AG051456NIH HHS S10 OD021548
6 · The paper itself

Abstract

Pediatric cancer treatment often involves chemotherapy and radiation, where off-target effects can include skeletal muscle decline. The effect of such treatments on juvenile skeletal muscle growth has yet to be investigated. We employed a small animal irradiator to administer fractionated hindlimb irradiation to juvenile mice bearing implanted rhabdomyosarcoma (RMS) tumors. Hindlimb-targeted irradiation (3 × 8.2 Gy) of 4-week-old mice successfully eliminated RMS tumors implanted one week prior. After establishment of this preclinical model, a cohort of tumor-bearing mice were injected with the chemotherapeutic drug, vincristine, alone or in combination with fractionated irradiation (5 × 4.8 Gy). Single myofiber analysis of fast-contracting extensor digitorum longus (EDL) and slow-contracting soleus (SOL) muscles was conducted 3 weeks post-treatment. Although a reduction in myofiber size was apparent, EDL and SOL myonuclear number were differentially affected by juvenile irradiation and/or vincristine treatment. In contrast, a decrease in myonuclear domain (myofiber volume/myonucleus) was observed regardless of muscle or treatment. Thus, inhibition of myofiber hypertrophic growth is a consistent feature of pediatric cancer treatment.

Indexed as

AgingAnimalsAntineoplastic Agents, PhytogenicCell Line, TumorChemoradiotherapyDisease Models, AnimalDose Fractionation, RadiationHindlimbHypertrophyMaleMice, Inbred C57BLMuscle Fibers, SkeletalRhabdomyosarcomaRotarod Performance TestTransplantation, IsogeneicVincristineAntineoplastic Agents, PhytogenicVincristine

Identifiers

PMID33177579
PMCPMC7659015

What OpenQuestion holds

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LicenceCC BY
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.