Evidence map›Paper›PMID 39852234›Full record

ArticleThe Journal of international medical research2025

High FGF18 expression levels predict poor prognosis in endometrial carcinoma patients and promote tumor growth and metastasis.

Zheng-Yao Lei, Jian Wu, Bao-Hua Zhang, Wei Xiang, Min Wang, Bin-Bin Li, Ming-Cheng Dai

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Article in The Journal of international medical research, 2025. 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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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Zheng-Yao LeiDepartment of Pathology, Tongji Hospital, Tongji University School of Medicine, Shanghai, China.
Jian WuDepartment of Pathology, Punan Branch of Renji Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.ORCID 0000-0003-2016-4275
Bao-Hua ZhangDepartment of Obstetrics and Gynecology, Punan Branch of Renji Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Wei XiangDepartment of Pathology, Punan Branch of Renji Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Min WangDepartment of Pathology, Punan Branch of Renji Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Bin-Bin LiDepartment of Pathology, Punan Branch of Renji Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Ming-Cheng DaiSchool of Clinical Medicine, Harbin Medical University, Harbin City, Heilongjiang, Province, China.ORCID 0000-0002-9987-3244

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate if fibroblast growth factor 18 (FGF18) expression plays an important role in endometrial carcinoma (EC).

methodsThe clinicopathological associations and prognostic value of FGF18 expression were retrospectively analyzed in 190 patients with EC. FGF18 expression was stably knocked down in EC cell lines. Changes in cell proliferation, migration, and invasion rates were examined via cell behavior experiments. Tumor growth was investigated using a xenograft mouse model. RNA sequencing (RNA-seq) was performed to identify differentially expressed genes (DEGs) in HEC-1-B cells after FGF18 knockdown, followed by pathway enrichment analysis of the DEGs.

resultsHigh FGF18 expression levels were closely correlated with EC clinicopathological features, such as histological subtype, FIGO stage, depth of myometrial invasion, and tumor size. Moreover, EC patients with high FGF18 expression levels had poorer overall survival. FGF18 knockdown in EC cells revealed its role in promoting tumor cell proliferation, migration, and invasion

conclusionsOverexpression of FGF18 may serve as a prognostic biomarker for EC patients and is a potential therapeutic target for treating this disease.

Indexed as

Biomarkers, TumorEndometrial NeoplasmsFibroblast Growth FactorsAgedAnimalsCell Line, TumorCell MovementCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansMiceMiddle AgedNeoplasm InvasivenessNeoplasm MetastasisPrognosisBiomarkers, Tumorfibroblast growth factor 18Fibroblast Growth Factorsbioinformaticsclinicopathological featureendometrial carcinomaFibroblast growth factor 18overall survivalprognostic biomarkerRNA sequencing

Identifiers

PMID39852234
PMCPMC11760137

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