Evidence map›Paper›PMID 38228655›Full record

ArticleScientific reports2024

Metformin protects ovarian granulosa cells in chemotherapy-induced premature ovarian failure mice through AMPK/PPAR-γ/SIRT1 pathway.

Yuxin Yang, Xiangting Tang, Ting Yao, Yiqing Zhang, Yufei Zhong, Shuqing Wu, Yurou Wang, Zezheng Pan

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
17.4field-weighted citation impact, top 1% of its field
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

26 citing papers in PubMed, 32 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Yuxin Yang *Faculty of Jiangxi Medical College, Nanchang University, No.461 Bayi Road, Donghu District, Nanchang City, 330006, Jiangxi Province, People's Republic of China.
Xiangting Tang *The Eighth Affiliated Hospital of Sun Yat-Sen University, Futian, Shenzhen, People's Republic of China.
Ting YaoFaculty of Jiangxi Medical College, Nanchang University, No.461 Bayi Road, Donghu District, Nanchang City, 330006, Jiangxi Province, People's Republic of China.
Yiqing ZhangFaculty of Jiangxi Medical College, Nanchang University, No.461 Bayi Road, Donghu District, Nanchang City, 330006, Jiangxi Province, People's Republic of China.
Yufei ZhongFaculty of Jiangxi Medical College, Nanchang University, No.461 Bayi Road, Donghu District, Nanchang City, 330006, Jiangxi Province, People's Republic of China.
Shuqing WuFaculty of Jiangxi Medical College, Nanchang University, No.461 Bayi Road, Donghu District, Nanchang City, 330006, Jiangxi Province, People's Republic of China.
Yurou WangFaculty of Jiangxi Medical College, Nanchang University, No.461 Bayi Road, Donghu District, Nanchang City, 330006, Jiangxi Province, People's Republic of China.
Zezheng PanFaculty of Jiangxi Medical College, Nanchang University, No.461 Bayi Road, Donghu District, Nanchang City, 330006, Jiangxi Province, People's Republic of China. panzz@ncu.edu.cn.
Nanchang University · CNEighth Affiliated Hospital of Sun Yat-sen University

Funding

National Natural Science Foundation of China 81860263Natural Science Foundation of Jiangxi Province 20192BAB205119
6 · The paper itself

Abstract

Premature ovarian failure (POF) caused by chemotherapy is a growing concern for female reproductive health. The use of metformin (MET), which has anti-oxidative and anti-inflammatory effects, in the treatment of POF damaged by chemotherapy drugs remains unclear. In this study, we investigated the impact of MET on POF caused by cyclophosphamide (CTX) combined with busulfan (BUS) and M1 macrophages using POF model mice and primary granule cells (GCs). Our findings demonstrate that intragastric administration of MET ameliorates ovarian damage and alleviates hormonal disruption in chemotherapy-induced POF mice. This effect is achieved through the reduction of inflammatory and oxidative stress-related harm. Additionally, MET significantly relieves abnormal inflammatory response, ROS accumulation, and senescence in primary GCs co-cultured with M1 macrophages. We also observed that this protective role of MET is closely associated with the AMPK/PPAR-γ/SIRT1 pathway in cell models. In conclusion, our results suggest that MET can protect against chemotherapy-induced ovarian injury by inducing the expression of the AMPK pathway while reducing oxidative damage and inflammation.

Indexed as

Antineoplastic AgentsMetforminPrimary Ovarian InsufficiencyAMP-Activated Protein KinasesAnimalsFemaleGranulosa CellsHumansMicePeroxisome Proliferator-Activated ReceptorsSirtuin 1AMP-Activated Protein KinasesAntineoplastic AgentsMetforminPeroxisome Proliferator-Activated ReceptorsSIRT1 protein, humanSirtuin 1

Identifiers

PMID38228655
PMCPMC10791659
OpenAlexW4390901435

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.