Evidence map›Paper›PMID 38706958›Full record

ArticleFunction (Oxford, England)2024

Long-term Musculoskeletal Consequences of Chemotherapy in Pediatric Mice.

Joshua R Huot, Patrick D Livingston, Fabrizio Pin, Connor R Thomas, Nicholas A Jamnick, Chandler S Callaway, Andrea Bonetto

Abstract read
In one paragraph

Article in Function (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. GL261 glioblastoma induces delayed body weight gain and stunted skeletal muscle growth in young mice.American journal of physiology. Regulatory, integrative and comparative physiology · 2025
    Article
  6. Diversity in chemotherapy-induced cachexia.American journal of physiology. Cell physiology · 2025
    Review
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

7 authors.

Joshua R HuotDepartment of Anatomy, Cell Biology and Physiology, Indiana University School of Medicine, Indianapolis, IN, 46202  USA.
Patrick D LivingstonDepartment of Kinesiology, School of Health and Human Sciences, Indiana University Purdue University Indianapolis, IN, 46202  USA.
Fabrizio PinDepartment of Anatomy, Cell Biology and Physiology, Indiana University School of Medicine, Indianapolis, IN, 46202  USA.
Connor R ThomasDepartment of Anatomy, Cell Biology and Physiology, Indiana University School of Medicine, Indianapolis, IN, 46202  USA.
Nicholas A JamnickDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, 80045  USA.
Chandler S CallawayDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, 80045  USA.
Andrea BonettoDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, 80045  USA.ORCID 0000-0002-3235-1871

Funding

Comprehensive Training Program in Musculoskeletal ResearchT32AR065971 · NIAMS · INDIANA UNIVERSITY INDIANAPOLIS · PI ALEXANDER G ROBLING · 2015 to 2026
$4.4M
Training Program in Cancer BiologyT32CA190216 · NCI · UNIVERSITY OF COLORADO DENVER · PI Craig T. Jordan · 2016 to 2026
$3.5M
Targeting RANKL for the treatment of muscle and bone defects in cachexiaR01AR079379 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI Andrea Bonetto · 2021 to 2026
$2.1M
IGFBP1 mediates a liver-bone-muscle axis in colorectal cancer cachexiaR01AR080051 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI Andrea Bonetto · 2022 to 2026
$2.1M
Interdisciplinary Training in Musculoskeletal ResearchT32AR080630 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI Karin A Payne, MICHAEL J ZUSCIK · 2022 to 2026
$1.7M
NCI NIH HHS T32 CA190216NIAMS NIH HHS R01 AR079379NIAMS NIH HHS R01 AR080051NIAMS NIH HHS T32 AR065971NIAMS NIH HHS T32 AR080630
6 · The paper itself

Abstract

Thanks to recent progress in cancer research, most children treated for cancer survive into adulthood. Nevertheless, the long-term consequences of anticancer agents are understudied, especially in the pediatric population. We and others have shown that routinely administered chemotherapeutics drive musculoskeletal alterations, which contribute to increased treatment-related toxicity and long-term morbidity. Yet, the nature and scope of these enduring musculoskeletal defects following anticancer treatments and whether they can potentially impact growth and quality of life in young individuals remain to be elucidated. Here, we aimed at investigating the persistent musculoskeletal consequences of chemotherapy in young (pediatric) mice. Four-week-old male mice were administered a combination of 5-FU, leucovorin, irinotecan (

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsAnimalsAntineoplastic AgentsCamptothecinFluorouracilIrinotecanLeucovorinMaleMiceMice, Inbred C57BLMuscle, SkeletalAntineoplastic AgentsCamptothecinFluorouracilIrinotecanLeucovorinbone masschemotherapyFolfirilong-term consequencesmouse modelsskeletal muscle

Identifiers

PMID38706958
PMCPMC11065107

What OpenQuestion holds

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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.