Evidence mapPaperPMID 42477307Full record

ArticleJournal of natural medicines2026

Quercetin attenuates cisplatin-induced muscle atrophy via Hippo/YAP1 signaling pathway.

Jingchun Lv, Jianwei Lin, Xiaojing Chen, Qi Wu, Zhiyao Cao, Dapeng Jiang

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Article in Journal of natural medicines, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Jingchun LvDepartment of Oncology (Ward 2), Shanghai Childrens Medical Center, Shanghai Jiao Tong University, Shanghai, China.
Jianwei LinDepartment of Oncology (Ward 2), Shanghai Childrens Medical Center, Shanghai Jiao Tong University, Shanghai, China.
Xiaojing ChenDepartment of Oncology (Ward 2), Shanghai Childrens Medical Center, Shanghai Jiao Tong University, Shanghai, China.
Qi WuDepartment of Oncology (Ward 2), Shanghai Childrens Medical Center, Shanghai Jiao Tong University, Shanghai, China.
Zhiyao CaoDepartment of Oncology (Ward 2), Shanghai Childrens Medical Center, Shanghai Jiao Tong University, Shanghai, China.
Dapeng JiangDepartment of Oncology (Ward 2), Shanghai Childrens Medical Center, Shanghai Jiao Tong University, Shanghai, China. jdp509@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Muscle wasting is a common event among cancer patients receiving chemotherapy treatment and has been reported to affect their survival. However, current therapies for counteracting this side effect are ineffective. This study investigates quercetin's efficacy against cisplatin-induced muscle atrophy and its mechanism. Using both C2C12 myotube and mouse models, we found quercetin pretreatment significantly alleviates cisplatin-induced muscle wasting. Mechanistically, transcriptome analysis identified that the Hippo signaling pathway was involved in cisplatin-induced muscle atrophy. Quercetin restored the activity of this pathway, including the expression and nuclear localization of its effector YAP1. Furthermore, quercetin mitigated cisplatin-induced muscle damage by improving mitochondrial membrane quality and function. Molecular docking revealed a direct interaction between quercetin and YAP1. Additionally, the possible interaction between YAP1 and mitochondrial function was revealed. Our findings demonstrate that quercetin attenuates cisplatin-induced muscle atrophy by modulating the Hippo/YAP1 pathway and preserving mitochondrial homeostasis, highlighting its therapeutic potential.

Indexed as

CisplatinMitochondrial dysfunctionMuscle atrophyQuercetinYAP1

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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 Socratic graph.