Evidence map›Paper›PMID 39192214›Full record

ArticleBMC cancer2024

Galaxamide alleviates cisplatin-induced premature ovarian insufficiency via the PI3K signaling pathway in HeLa tumor-bearing mice.

Huan Tao, Zongbin Chen, Bo Yao, Xinyi Ren, Hanlin Shuai, Shihai Xu, Qingbing Zha, Ping Li

Abstract read
In one paragraph

Article in BMC cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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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

4 citing papers in PubMed.

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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.

Huan TaoCenter of Reproductive Medicine, First Affiliated Hospital of Jinan University, Guangzhou, 510630, China.
Zongbin ChenDepartment of Gynecology & Obstetrics, First Affiliated Hospital of Jinan University, Guangzhou, 510630, China.
Bo YaoDepartment of Pathology, Jinan University School of Medicine, Guangzhou, 510632, China.
Xinyi RenDepartment of Pathology, Jinan University School of Medicine, Guangzhou, 510632, China.
Hanlin ShuaiDepartment of Gynecology & Obstetrics, First Affiliated Hospital of Jinan University, Guangzhou, 510630, China.
Shihai XuDepartment of Chemistry, College of Chemistry and Material Science, Jian University, Guangzhou, 510632, China. txush@jnu.edu.cn.
Qingbing ZhaCenter of Reproductive Medicine, First Affiliated Hospital of Jinan University, Guangzhou, 510630, China. zhaqingbb@sina.com.
Ping LiDepartment of Pathology, Jinan University School of Medicine, Guangzhou, 510632, China. pinger355@126.com.

Funding

Basic and Applied Basic Research Foundation of Guangdong Province 2024A1515011821
6 · The paper itself

Abstract

backgroundIt is challenging to improve the effects of chemotherapy and reduce its adverse impact on the ovaries. Our previous study suggested that the combination of galaxamide could enhance the antitumor effect of cisplatin (CIS) in HeLa cell xenograft mice. However, their potential effects on ovarian tissues remain unknown.

methodsThe Hela tumor-bearing female BALB/c mice model was established and randomly divided into three groups: control group (PBS group), CIS group (0.3 mg/kg CIS group) and galaxamide group (0.3 mg/kg CIS + 3 mg/kg galaxamide-treated group). The serum sex hormones levels, ovarian morphology, functional and molecular characterisation were determined and compared with those of the control group.

resultsThe hormonal effects indicated premature ovarian insufficiency (POI) associated with CIS-induced tumor-bearing mice. CIS induces the apoptosis in primordial and developing follicles and subsequently increases follicular atresia, eventually leading to follicle loss. After cotreatment, galaxamide significantly increased anti-Mullerian hormone (AMH) and follicle-stimulating hormone receptor (FSHR) expression and prevented the CIS-induced PI3K pathway, which triggers follicle activation, apoptosis or atresia.

conclusionThese findings demonstrate that galaxamide could attenuate CIS-induced follicle loss by acting on the PI3K signaling pathway by stimulating AMH and/or FSHR and thus provides promising therapeutic options for patients with cervical cancer.

Indexed as

CisplatinPhosphatidylinositol 3-KinasesPrimary Ovarian InsufficiencySignal TransductionAnimalsAnti-Mullerian HormoneAntineoplastic AgentsApoptosisFemaleHeLa CellsHumansMiceMice, Inbred BALB CReceptors, FSHUterine Cervical NeoplasmsXenograft Model Antitumor AssaysAnti-Mullerian HormoneAntineoplastic AgentsCisplatinPhosphatidylinositol 3-KinasesReceptors, FSHCisplatinPremature ovarian insufficiencySeaweedTumor-bearing

Identifiers

PMID39192214
PMCPMC11350984

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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.