Evidence map›Paper›PMID 40136406›Full record

ArticleCurrent issues in molecular biology2025

The Protective Effects of Perch Essence Against Muscle Atrophy in Cancer Cachexia and Cisplatin Treatment.

Shu-Lan Yeh, Pei-Yin Chen, Jiunn-Wang Liao, Ruo-Li Huang, Shu-Han Yu, Ling-Ni Chen, Mao-Hsiang Lee, Li-Wen Chen, Haw-Wen Chen, Ya-Chen Yang and 2 more

Abstract read
In one paragraph

Article in Current issues in molecular biology, 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

12 authors.

Shu-Lan YehDepartment of Nutrition, Chung Shan Medical University, Taichung 40203, Taiwan.
Pei-Yin ChenDepartment of Senior Citizen Welfare and Long-Term Care Business (Master Program), Hungkuang University, Taichung 433304, Taiwan.
Jiunn-Wang LiaoGraduate Institute of Veterinary Pathology, College of Veterinary Medicine, National Chung Hsing University, Taichung 402202, Taiwan.ORCID 0000-0001-7374-1203
Ruo-Li HuangDepartment of Nutrition, Chung Shan Medical University, Taichung 40203, Taiwan.
Shu-Han YuDepartment of Nutrition, Chung Shan Medical University, Taichung 40203, Taiwan.
Ling-Ni ChenAnyong Biotechnology Inc., Kaohsiung 827012, Taiwan.ORCID 0000-0001-7442-463X
Mao-Hsiang LeeAnyong Biotechnology Inc., Kaohsiung 827012, Taiwan.ORCID 0009-0007-2792-4763
Li-Wen ChenDivision of Nutrition Therapy, Jen-Ai Hospital, Taichung 412224, Taiwan.
Haw-Wen ChenDepartment of Nutrition, China Medical University, Taichung 40402, Taiwan.ORCID 0000-0001-7611-5515
Ya-Chen YangDepartment of Health and Nutrition Biotechnology, Asia University, Taichung 413, Taiwan.
Yu-Ling WuCardiovascular and Mitochondrial Related Disease Research Center, Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Hualien 970, Taiwan.
Kai-Li LiuDepartment of Nutrition, Chung Shan Medical University, Taichung 40203, Taiwan.

Funding

China Medical University and Asia University CMU103-ASIA-06Chung Shan Medical University CSMU-INT-113-06 and CSMU-INT-113-17
6 · The paper itself

Abstract

Muscle atrophy, through several pathways including increased protein catabolism, leads to adverse effects in cachexia induced by cancer and chemotherapy. Perch essence (PE) is a perch extract rich in branched-chain amino acids and peptides. The present study initially investigated the effects of PE supplementation on muscle atrophy in a mouse model of cancer cachexia induced by C26 cancer cells and compared these effects with those of tryptone. Compared with the tumor-only group, we found that PE supplementation significantly improved body weight, muscle mass, maximum limb grip strength (MLGS), and myosin heavy chain expression in the muscles of tumor-bearing mice. PE also significantly inhibited the expression of factors related to protein degradation, oxidative stress, and inflammation, while enhancing the expression of antioxidant enzymes in tumor-bearing mice. These effects of PE were associated with an increased expression of phosphorylated Akt and forkhead box protein O1, along with a reduced expression of phosphorylated nuclear factor-κB p65 in the muscles of tumor-bearing mice. Furthermore, PE similarly increased MLGS and attenuated muscle atrophy in mice exposed to cisplatin by inhibiting protein degradation. All the therapeutic effects of PE supplementation mentioned above were generally greater than those of tryptone supplementation. These results suggest the potential of PE in protecting against muscle atrophy induced by tumors or chemotherapy.

Indexed as

cancer cachexiacisplatinmuscle atrophyperch essence

Identifiers

PMID40136406
PMCPMC11941385

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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.