空军军医大学学报2024,Vol.45Issue(10) :1165-1170.DOI:10.13276/j.issn.2097-1656.2024.10.016

脂肪酸结合蛋白3在肾透明细胞癌中的表达及其意义

Expression and significance of fatty acid-binding protein 3 in clear cell renal cell carcinoma

沈旭峰 向安平 汪宁 陈晓农 王荣江
空军军医大学学报2024,Vol.45Issue(10) :1165-1170.DOI:10.13276/j.issn.2097-1656.2024.10.016

脂肪酸结合蛋白3在肾透明细胞癌中的表达及其意义

Expression and significance of fatty acid-binding protein 3 in clear cell renal cell carcinoma

沈旭峰 1向安平 1汪宁 1陈晓农 1王荣江1
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作者信息

  • 1. 湖州师范学院附属第一医院/湖州市第一人民医院泌尿外科,浙江湖州 313000
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摘要

目的 探讨脂肪酸结合蛋白3(FABP3)在肾透明细胞癌(ccRCC)中的表达及其与ccRCCTNM分期、病理分级及预后的相关性.方法 收集湖州师范学院附属第一医院因ccRCC行根治术的患者的癌组织标本及癌旁非癌性组织标本100份,通过qRT-PCR、IHC检测所有ccRCC患者标本FABP3的表达水平.采用WHO/ISUP分级系统对ccRCC进行病理分级,一共4级,Gl、G2、G3、G4;根据ccRCC的TNM分期将ccRCC患者标本分为Ⅰ期、Ⅱ期、Ⅲ期和Ⅳ期,比较各分组或分期FABP3表达的差异,并分析FABP3表达高低与ccRCC患者总生存期(OS)的相关性.结果 qRT-PCR、IHC结果显示FABP3在ccRCC组织中的表达显著高于癌旁非癌性组织(P<0.05).在 WHO/ISUP 分级中,FABP3 的表达水平 G4 组(0.94±0.08)显著高于 G1(0.61±0.08)、G2(0.72±0.07)以及G3(0.82±0.09),差异具有统计学意义(P<0.001).在TNM分期中,FABP3的表达水平Ⅰ期(0.64±0.06)低于Ⅱ期(0.76±0.03),Ⅲ期(0.84±0.02)高于Ⅱ期,而Ⅳ期(0.92±0.04)显著高于Ⅲ期,差异具有统计学意义(P<0.001).FABP3表达水平与ccRCC的TNM分期、WHO/ISUP分级显著正相关(P<0.05).Cox 分析显示,FABP3 高表达(HR=2.21,95%CI:1.47~2.95,P<0.001),TNM 分期中的Ⅲ期(HR=1.41,95%CI:1.07~2.61,P=0.01)和Ⅳ期(HR=2.65,95%CI:1.26~3.23,P<0.001),WHO/ISUP分级中的 G3(HR=1.25,95%CI:1.05~2.95,P=0.014)与 G4(HR=2.87,95%CI:1.54~3.60,P<0.001)是ccRCC患者预后不良的危险因素.结论 在ccRCC患者中,FABP3呈现出高表达趋势,且其高表达与ccRCC的预后不良相关,这提示着FABP3可能可以作为预测ccRCC预后的潜在分子标志物,为进一步研究ccRCC的分子机制和后续治疗策略提供了理论基础.

Abstract

Objective To investigate the expression of fatty acid-binding protein 3(FABP3)in clear cell renal cell carcinoma(ccRCC)and its correlation with TNM staging,pathological grading,and prognosis of ccRCC.Methods The study collected 100 cancer tissue samples and adjacent non-cancerous tissue samples from patients who underwent radical surgery for ccRCC at First Affiliated Hospital of Huzhou University.The expression levels of FABP3 in all ccRCC samples were detected using qRT-PCR and IHC.WHO/ISUP grading system was used for pathological grading of ccRCC,with a total of 4 grades:G1,G2,G3,and G4.Based on the TNM staging,samples were categorized into stages Ⅰ,Ⅱ,Ⅲ,andⅣ.The differences in FABP3 expression among various groups and stages were compared,and the correlation between FABP3 expression levels and overall survival(OS)of ccRCC patients was analyzed.Results qRT-PCR and IHC results showed that FABP3 expression in ccRCC tissues was significantly higher than that in adjacent non-cancerous tissues(P<0.05).In the WHO/ISUP grading system,the expression level of FABP3 in G4 group(0.94±0.08)was significantly higher than that in G1(0.61±0.08),G2(0.72±0.07),and G3(0.82±0.09),and the difference was statistically significant(P<0.001).In the TNM staging,the expression level of FABP3 in stage Ⅰ(0.64±0.06)was lower than that in stage Ⅱ(0.76±0.03),that in stage Ⅲ(0.84±0.02)was higher than that in stage Ⅱ,and that in stage Ⅳ(0.92±0.04)was significantly higher than that in stage Ⅲ,with statistically significant difference(P<0.001).The expression level of FABP3 was significantly positively correlated with TNM staging and WHO/ISUP grading of ccRCC(P<0.05).Cox analysis showed that high expression of FABP3(HR=2.21,95%CI:1.47-2.95,P<0.001),stage Ⅲ(HR=1.41,95%CI:1.07-2.61,P=0.01)and stage Ⅳ(HR=2.65,95%CI:1.26-3.23,P<0.001)in TNM staging,and G3(HR=1.25,95%CI:1.05-2.95,P=0.014)and G4(HR=2.87,95%CI:1.54-3.60,P<0.001)in WHO/ISUP grading were risk factors for poor prognosis in patients with ccRCC.Conclusion In ccRCC patients,FABP3 is highly expressed,and its high expression is related to poor prognosis of ccRCC,which suggests that FABP3 may serve as a potential molecular marker for predicting ccRCC prognosis,providing a theoretical basis for further research into the molecular mechanisms and subsequent treatment strategies of ccRCC.

关键词

脂肪酸结合蛋白3/肾透明细胞癌/WHO/ISUP分级/TNM分期

Key words

fatty acid-binding protein 3/clear cell renal cell carcinoma/WHO/ISUP grading/TNM staging

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基金项目

浙江省医药卫生科技计划项目(2024KY1647)

湖州市科学技术局公益性应用研究项目(2020GYB30)

湖州市科学技术局公益性应用研究项目(2023GYB40)

出版年

2024
空军军医大学学报
第四军医大学

空军军医大学学报

CHSSCD
影响因子:0.372
ISSN:2097-1656
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