Evidence map›Paper›PMID 40691041›Full record

ArticleAmerican journal of physiology. Cell physiology2025

B0092 tumor-bearing mice are a new model for the study of cachexia in head and neck cancer.

Patrick D Livingston, Ana Luiza Labbate Bonaldo, Nicholas A Jamnick, Natalia M Weinzierl, Caleb J Gammon, Chandler S Callaway, Schuyler Lee, Bifeng Gao, Andrew Goodspeed, Robson F Carvalho and 5 more

Abstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

15 authors.

Patrick D LivingstonDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States.
Ana Luiza Labbate BonaldoDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States.ORCID 0000-0001-6825-9164
Nicholas A JamnickDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States.ORCID 0000-0003-0890-2853
Natalia M WeinzierlDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States.
Caleb J GammonDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States.
Chandler S CallawayDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States.
Schuyler LeeDepartment of Medicine-Pulmonary Sciences and Critical Care, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States.
Bifeng GaoDepartment of Medicine-Pulmonary Sciences and Critical Care, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States.
Andrew GoodspeedDepartment of Biomedical Informatics, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States.
Robson F CarvalhoDepartment of Structural and Functional Biology, Institute of Biosciences, São Paulo State University (UNESP), Botucatu, São Paulo, Brazil.
Christian D YoungDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States.
David J OrlickyDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States.ORCID 0000-0002-0417-1400
Douglas J AdamsDepartment of Orthopedics, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States.
Leah J NovingerDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States.ORCID 0000-0002-9018-7838
Andrea BonettoDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States.ORCID 0000-0002-3235-1871

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
PILOT STUDY--SUBSTRATE METABOLISM IN EXTREMELY LOW BIRTH WEIGHT INFANTSP30DK048520 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI JANINE A HIGGINS · 1995 to 2026
$32.6M
Treating recurrent HNSCC with radiation and dual TGF-Beta/PD-L1.P50CA261605 · NCI · UNIVERSITY OF COLORADO DENVER · PI LUCIA, M. SCOTT · 2021 to 2025
$10.1M
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
American Cancer Society (ACS) 132013-RSG-18-010-01-CCGCancer League of Colorado (CLC) AWD-242527-ABDepartment of Pathology University of ColoradoHHS | NIH | National Cancer Institute (NCI) P50CA261605HHS | NIH | National Cancer Institute (NCI) T32CA190216HHS | NIH | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) R01AR079379HHS | NIH | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) R01AR080051HHS | NIH | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) T32AR080630NCI NIH HHS P30 CA046934NCI NIH HHS P50 CA261605NCI NIH HHS T32 CA190216NIAMS NIH HHS R01 AR079379NIAMS NIH HHS R01 AR080051NIAMS NIH HHS T32 AR080630NIDDK NIH HHS P30 DK048520University of Colorado Cancer Center
6 · The paper itself

Abstract

Head and neck cancer (HNC) accounts for ∼4% of all cancers but causes ∼15,000 deaths annually in the United States. Over 40% of HNC patients present with cachexia, a severe comorbidity associated with skeletal muscle defects, worsened treatment response, and poor outcomes. The mechanisms behind HNC cachexia remain unclear, partly due to limited small animal models. This study characterizes functional and molecular features of cachexia in a novel preclinical model using tobacco-induced B0092 oral squamous cell carcinoma in C57BL/6J mice. C2C12 myotubes were exposed to various concentrations of B0092 conditioned media (CM) to assess effects on myotube diameter and expression of muscle-specific ubiquitin ligases (MuRF-1 and atrogin-1). C57BL/6J male and female mice were implanted with B0092 cells (5 × 10

Indexed as

CachexiaHead and Neck NeoplasmsSquamous Cell Carcinoma of Head and NeckAnimalsCell Line, TumorDisease Models, AnimalFemaleMaleMiceMice, Inbred C57BLMuscle Fibers, SkeletalMuscle ProteinsMuscle, SkeletalMuscular AtrophySKP Cullin F-Box Protein LigasesTripartite Motif ProteinsFbxo32 protein, mouseMuscle ProteinsSKP Cullin F-Box Protein LigasesTrim63 protein, mouseTripartite Motif ProteinsUbiquitin-Protein Ligasesbone losscachexiahead and neck cancermuscle wastingmuscle weakness

Identifiers

PMID40691041
PMCPMC12352498

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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.