Evidence map›Paper›PMID 41419070›Full record

ReviewBiochimica et biophysica acta. Molecular basis of disease2026

The effects of tissue inflammation on cancer cachexia.

Benjamin R Pryce, Haiming L Kerr

Abstract readReview
In one paragraph

Review in Biochimica et biophysica acta. Molecular basis of disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Benjamin R PryceDepartment of Medicine, Division of Gastroenterology, University of Washington, Seattle, Washington, USA. Electronic address: bpryce@uw.edu.
Haiming L KerrDepartment of Medicine, Division of Gerontology and Geriatric Medicine, University of Washington School of Medicine, WA, Seattle, USA; Geriatric Research, Education and Clinical Center, Veterans Affairs Puget Sound Health Care System, Seattle, WA, 98108, USA. Electronic address: haiml@uw.edu.

Funding

The Role of AMPK in Regulating Muscle Mass and Function in Cancer CachexiaK01AR080787 · NIAMS · UNIVERSITY OF WASHINGTON · PI Haiming Liu Kerr · 2023 to 2026
$488k
NIAMS NIH HHS K01 AR080787
6 · The paper itself

Abstract

Cancer cachexia is characterized by a significant loss in body weight due to the wasting of skeletal muscle and adipose tissue. Systemic inflammation has long been associated with cachexia, with various tumor secreted factors shown to correlate with as well as cause tissue wasting. In addition to systemic inflammation, it has become increasingly appreciated that inflammation occurs in specific tissues in cancer cachexia, with tissues such as muscle, adipose, liver and brain being affected. While several studies have shown that this local tissue inflammation contributes to cachexia, there is evidence that some aspects of the inflammatory response may play a protective role to mitigate tissue wasting. Here, we will review the findings on local tissue inflammation in cachexia, comparing the impacts of such inflammation on tissue wasting and cachexia progression overall. Furthermore, we discuss the methods used to mitigate inflammation in various tissues and highlight the outcomes on the cachectic phenotype. Collectively, understanding how inflammation contributes to cachexia in each tissue will ultimately influence how therapies can be designed to treat cachexia while minimizing possible adverse side effects.

Indexed as

CachexiaInflammationNeoplasmsAdipose TissueAnimalsHumansLiverMuscle, SkeletalCancer CachexiaInflammationMacrophage

Identifiers

PMID41419070
PMCPMC12767137

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.