Evidence map›Paper›PMID 40973862›Full record

ArticleJournal of assisted reproduction and genetics2025

Inhibition of integrated stress response by ISRIB promotes mouse and human primordial follicle activation via the mTOR pathway.

Tiantian Hao, Weiyong Wang, Ziyong Zhao, Zhenyu Zhou, Wenbo Zhang, Yashuang Weng, Longwei Gao, Hongwei Wei, Wenjun Zhou, Shuang Liu and 2 more

Abstract read
In one paragraph

Article in Journal of assisted reproduction and genetics, 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. Article
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.

Tiantian Hao *The Innovation Centre of Ministry of Education for Development and Diseases, School of Medicine, South China University of Technology, Guangzhou Higher Education Mega Center, 382 Outer Ring East Road, Guangdong, 510006, China.
Weiyong Wang *The Innovation Centre of Ministry of Education for Development and Diseases, School of Medicine, South China University of Technology, Guangzhou Higher Education Mega Center, 382 Outer Ring East Road, Guangdong, 510006, China.
Ziyong ZhaoCenter for Reproductive Medicine, Zhongshan City People's Hospital, 2 Sunwen East Road, Guangdong, 528403, China.
Zhenyu ZhouThe First Clinical College of Hainan Medical University, Haikou, 570102, China.
Wenbo ZhangThe Innovation Centre of Ministry of Education for Development and Diseases, School of Medicine, South China University of Technology, Guangzhou Higher Education Mega Center, 382 Outer Ring East Road, Guangdong, 510006, China.
Yashuang WengThe Innovation Centre of Ministry of Education for Development and Diseases, School of Medicine, South China University of Technology, Guangzhou Higher Education Mega Center, 382 Outer Ring East Road, Guangdong, 510006, China.
Longwei GaoThe Innovation Centre of Ministry of Education for Development and Diseases, School of Medicine, South China University of Technology, Guangzhou Higher Education Mega Center, 382 Outer Ring East Road, Guangdong, 510006, China.
Hongwei WeiThe Innovation Centre of Ministry of Education for Development and Diseases, School of Medicine, South China University of Technology, Guangzhou Higher Education Mega Center, 382 Outer Ring East Road, Guangdong, 510006, China.
Wenjun ZhouThe Innovation Centre of Ministry of Education for Development and Diseases, School of Medicine, South China University of Technology, Guangzhou Higher Education Mega Center, 382 Outer Ring East Road, Guangdong, 510006, China.
Shuang LiuThe Innovation Centre of Ministry of Education for Development and Diseases, School of Medicine, South China University of Technology, Guangzhou Higher Education Mega Center, 382 Outer Ring East Road, Guangdong, 510006, China.
Meijia ZhangThe Innovation Centre of Ministry of Education for Development and Diseases, School of Medicine, South China University of Technology, Guangzhou Higher Education Mega Center, 382 Outer Ring East Road, Guangdong, 510006, China. zhangmeijia@scut.edu.cn.ORCID http://orcid.org/0000-0001-7803-3054
Yuezhou ChenCenter for Reproductive Medicine, Zhongshan City People's Hospital, 2 Sunwen East Road, Guangdong, 528403, China. yzchen415@126.com.

Funding

the Guangdong Basic and Applied Basic Research Foundation 2022A1515220206the National Key Research and Development Program of China 2022YFC2703000the National Natural Science Foundation of China 32270900the National Natural Science Foundation of China U24A20662
6 · The paper itself

Abstract

purposeThe aim of this study is to investigate the effect of integrated stress response (ISR) inhibitor (ISRIB) on primordial follicle activation.

methodsWe identified drugs promoting primordial follicle activation and investigated their mechanisms through culturing newborn mouse ovaries in vitro. Validation was performed in vivo through intraperitoneal injection in newborn mice. Additionally, we analyzed its potential mechanisms through transcriptome sequencing. Finally, the function and mechanisms of ISRIB were further validated through culturing human ovarian tissues in vitro.

resultsISR activity was present in neonatal mouse ovaries. ISRIB in vitro culture and in vivo intraperitoneal injection significantly decreased the protein levels of phosphorylated eukaryotic translation initiation factor 2 subunit alpha (p-eIF2α) and activating transcription factor 4 (ATF4). ISRIB also significantly increased the growing follicle number and the protein levels of phosphorylated mammalian target of rapamycin (p-mTOR), KIT ligand (KITL), phosphorylated protein kinase B (p-Akt), and phosphorylated forkhead Box O3a (p-FOXO3a) in neonatal mouse ovaries and/or cultured human ovarian fragments. ISRIB significantly increased the relative fluorescence intensities of p-mTOR in the pre-granulosa cells of primordial follicles, and ISRIB-induced increase of p-Akt and p-FOXO3a was completely reversed by KIT inhibitor ISCK03. In the excessive ISR mouse model induced by corticosterone, ISRIB could partially reverse the apoptosis of primordial and growing follicles.

conclusionISRIB promoted mouse and human primordial follicle activation via the mTOR pathway and partly reversed corticosterone-induced decrease of growing follicles. These results suggest that ISRIB may be a potential drug for rescuing infertility in POI patients.

Indexed as

Ovarian FollicleStress, PhysiologicalTOR Serine-Threonine KinasesActivating Transcription Factor 4AnimalsAnimals, NewbornFemaleForkhead Box Protein O3HumansMiceOvaryProto-Oncogene Proteins c-aktSignal TransductionStem Cell FactorActivating Transcription Factor 4Forkhead Box Protein O3MTOR protein, humanmTOR protein, mouseProto-Oncogene Proteins c-aktStem Cell FactorTOR Serine-Threonine KinasesIntegrated stress responseISRIBMTORPremature ovarian insufficiencyPrimordial follicle activation

Identifiers

PMID40973862
PMCPMC12705521

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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.