Evidence map›Paper›PMID 40632209›Full record

ArticleCalcified tissue international2025

Decreased Expression and Secretion of the Myokine Fndc5/Irisin by Cisplatin Treatment in Mouse Skeletal Muscle.

Yu Miyauchi, Shinki Soga, Hayato Nanri, Shiori Yonamine, Takayuki Ogiwara, Miho Kiyama, Risako Kon, Nobutomo Ikarashi, Yoshihiko Chiba, Tomoo Hosoe and 1 more

Abstract read
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Article in Calcified tissue international, 2025. 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

11 authors.

Yu MiyauchiDepartment of Biomolecular Pharmacology, School of Pharmacy and Pharmaceutical Science, Hoshi University, 2-4-41 Ebara, Shinagawa-Ku, Tokyo, 1428501, Japan.
Shinki SogaDepartment of Biomolecular Pharmacology, School of Pharmacy and Pharmaceutical Science, Hoshi University, 2-4-41 Ebara, Shinagawa-Ku, Tokyo, 1428501, Japan.
Hayato NanriDepartment of Biomolecular Pharmacology, School of Pharmacy and Pharmaceutical Science, Hoshi University, 2-4-41 Ebara, Shinagawa-Ku, Tokyo, 1428501, Japan.
Shiori YonamineDepartment of Biomolecular Pharmacology, School of Pharmacy and Pharmaceutical Science, Hoshi University, 2-4-41 Ebara, Shinagawa-Ku, Tokyo, 1428501, Japan.
Takayuki OgiwaraDepartment of Biomolecular Pharmacology, School of Pharmacy and Pharmaceutical Science, Hoshi University, 2-4-41 Ebara, Shinagawa-Ku, Tokyo, 1428501, Japan.
Miho KiyamaDepartment of Biomolecular Pharmacology, School of Pharmacy and Pharmaceutical Science, Hoshi University, 2-4-41 Ebara, Shinagawa-Ku, Tokyo, 1428501, Japan.
Risako KonDepartment of Biomolecular Pharmacology, School of Pharmacy and Pharmaceutical Science, Hoshi University, 2-4-41 Ebara, Shinagawa-Ku, Tokyo, 1428501, Japan.
Nobutomo IkarashiDepartment of Biomolecular Pharmacology, School of Pharmacy and Pharmaceutical Science, Hoshi University, 2-4-41 Ebara, Shinagawa-Ku, Tokyo, 1428501, Japan.
Yoshihiko ChibaLaboratory of Molecular Biology and Physiology, School of Pharmacy and Pharmaceutical Science, Hoshi University, 2-4-41 Ebara, Shinagawa-Ku, Tokyo, 1428501, Japan.
Tomoo HosoeDepartment of Biomolecular Pharmacology, School of Pharmacy and Pharmaceutical Science, Hoshi University, 2-4-41 Ebara, Shinagawa-Ku, Tokyo, 1428501, Japan.
Hiroyasu SakaiDepartment of Biomolecular Pharmacology, School of Pharmacy and Pharmaceutical Science, Hoshi University, 2-4-41 Ebara, Shinagawa-Ku, Tokyo, 1428501, Japan. sakai@hoshi.ac.jp.ORCID http://orcid.org/0000-0002-4501-2836

Funding

JSPS KAKENHI Grant-in-Aid for Scientific Research (C) 22K06869
6 · The paper itself

Abstract

The systemic administration of cisplatin has been shown to substantially reduce skeletal muscle mass. This is a serious concern, as muscle loss is correlated with increased mortality in patients with cancer. Cisplatin also contributes to cognitive decline, but the exact mechanism thereof remains unclear. In this study, we focused on fibronectin type III domain-containing 5 (Fndc5), a gene that produces irisin, a myokine that is important for brain health. Male C57BL/6J mice (8-9 weeks old) were injected with cisplatin or saline for 4 consecutive days. Twenty-four h after final injection of cisplatin, quadriceps muscles were isolated. C2C12 myotubes were treated with cisplatin with/without AICAR. In male C57BL/6J mice treated with cisplatin, a reduced expression of the key regulator PGC-1α was observed, along with reduced levels of Fndc5/irisin mRNA and protein in the mice quadriceps muscles. Similar findings were seen in cisplatin-treated C2C12 myotube cells, where the activation of PGC-1α with AICAR partially offset these effects. These results suggest that cisplatin inhibits the synthesis of Fndc5/irisin and may contribute to the metabolic changes and cognitive decline observed in patients with cancer who receive this treatment.

Indexed as

Antineoplastic AgentsCisplatinFibronectinsMuscle, SkeletalAnimalsMaleMiceMice, Inbred C57BLMuscle Fibers, SkeletalMyokinesAntineoplastic AgentsCisplatinFibronectinsFNDC5 protein, mouseMyokinesAnticancer drugsCisplatinIrisinMuscle atrophyPGC-1αSide effects

Identifiers

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.