FOLR1在宫颈鳞状细胞癌中表达上调并与患者的无进展生存率相关

IF 0.5 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Pteridines Pub Date : 2020-01-01 DOI:10.1515/pteridines-2020-0014
Lingling Xie, Qingwen Li, Mei-Ping Zhang, Xia Sun, Zhongyu Xi, Aiyun Sun
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Eighty one cervical squamous cell cancer patients who received surgery were included for FOLR1 protein expression detected by immunohistochemistry assay (IHC). The correlation between FOLR1 protein expression and patients’ clinical features was analyzed. Results FOLR1 mRNA was up-regulated in tumor tissue compared to corresponding normal cervical tissue of cervical squamous cell carcinoma. Top 20 genes interacted with FOLR1 was identified through the network with the edges of 146. UBXN10 (r=0.668, P<0.01) and GBP6 (r-=0.606, P<0.01) were the top 2 genes that most correlated with FOLR1. The serum level of FR-α (FOLR1 coding protein) were 275.50±83.79 and 161.70±66.62 (ng/L) for the cervical cancer and healthy control subjects respectively with significant statistical difference (P<0.05). Using the serum FR-α as serological marker for cervical cancer detection, the diagnostic sensitivity, specificity and AUC were 80.0% (58.40% to 91.93%), 80.65% (63.72% to 90.81%) and 0.85(95%CI:0.74-0.96), respectively. Immunohistochemical assay indicated that of the 81 cancer tissue samples, 45 (55.6%) was FOLR1 protein positive. FOLR1 protein positive expression rate in FIGO stage Ⅲ/Ⅳ was significant higher than in the stage Ⅰ/Ⅱ with statistical difference (P<0.05). The progression free survival (PFS) was significant different between FOLR1 high and low expression group (HR=2.48, 95%CI:1.1-5.58, P=0.023). However, the overall survival (OS) was not statistical different between the two groups (HR=1.34, 95%CI:0.84-2.15, P=0.22). 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引用次数: 1

摘要

目的探讨叶酸受体1 (FOLR1)在宫颈鳞状细胞癌中的表达及其临床意义。方法在多发性肿瘤肿瘤基因组图谱(TCGA)数据库中检测FOLR1 mRNA表达水平。通过GEPIA在线数据分析工具比较宫颈鳞癌患者肿瘤组织与正常宫颈组织中FOLR1 mRNA的相对表达量。采用log-rank检验比较FOLR1高表达组和低表达组的总生存期(OS)和无进展生存期(PFS)。选取31例宫颈鳞癌患者和20例健康对照者进行血清FOLR1蛋白水平检测。采用免疫组化法(IHC)检测81例宫颈鳞癌手术患者FOLR1蛋白表达。分析FOLR1蛋白表达与患者临床特征的相关性。结果与宫颈鳞癌正常组织相比,FOLR1 mRNA在肿瘤组织中表达上调。通过网络鉴定出与FOLR1互作最多的20个基因,边数为146。UBXN10 (r=0.668, P<0.01)和GBP6 (r-=0.606, P<0.01)是与FOLR1最相关的前2个基因。宫颈癌患者与健康对照组血清FR-α (FOLR1编码蛋白)水平分别为275.50±83.79、161.70±66.62 (ng/L),差异有统计学意义(P<0.05)。采用血清FR-α作为宫颈癌的血清学标志物,诊断敏感性为80.0%(58.40% ~ 91.93%),特异性为80.65% (63.72% ~ 90.81%),AUC为0.85(95%CI:0.74 ~ 0.96)。免疫组化检测结果显示,81例癌组织标本中有45例(55.6%)为FOLR1蛋白阳性。FIGO期Ⅲ/ⅣFOLR1蛋白阳性表达率显著高于Ⅰ/Ⅱ期,差异有统计学意义(P<0.05)。FOLR1高、低表达组患者无进展生存期(PFS)差异有统计学意义(HR=2.48, 95%CI:1.1 ~ 5.58, P=0.023)。两组患者总生存期(OS)差异无统计学意义(HR=1.34, 95%CI:0.84 ~ 2.15, P=0.22)。结论:FOLR1在宫颈鳞状细胞癌的血清和癌组织中均表达上调,可能对宫颈鳞状细胞癌具有诊断和预后作用。
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FOLR1 was up-regulated in cervical squamous cell carcinoma and correlated with the patients’ progression free survival
Abstract Objective The aim of the present work was to evaluate the folate-receptor 1 (FOLR1) expression in cervical squamous cell carcinoma and its clinical significance. Methods FOLR1 mRNA expression level was detected in the cancer genome atlas (TCGA) database for multiple carcinomas. The FOLR1 mRNA relative expression between tumor tissue and normal cervix tissue of the cervical squamous cell cancer patients was compared by the online data analysis tool of GEPIA. The overall survival (OS) and progression free survival (PFS) between the FOLR1 high and low expression groups were compared by the log-rank test. Thirty one cervical squamous cancer patients and 20 healthy controls were included in and tested for serum FOLR1 protein level detection. Eighty one cervical squamous cell cancer patients who received surgery were included for FOLR1 protein expression detected by immunohistochemistry assay (IHC). The correlation between FOLR1 protein expression and patients’ clinical features was analyzed. Results FOLR1 mRNA was up-regulated in tumor tissue compared to corresponding normal cervical tissue of cervical squamous cell carcinoma. Top 20 genes interacted with FOLR1 was identified through the network with the edges of 146. UBXN10 (r=0.668, P<0.01) and GBP6 (r-=0.606, P<0.01) were the top 2 genes that most correlated with FOLR1. The serum level of FR-α (FOLR1 coding protein) were 275.50±83.79 and 161.70±66.62 (ng/L) for the cervical cancer and healthy control subjects respectively with significant statistical difference (P<0.05). Using the serum FR-α as serological marker for cervical cancer detection, the diagnostic sensitivity, specificity and AUC were 80.0% (58.40% to 91.93%), 80.65% (63.72% to 90.81%) and 0.85(95%CI:0.74-0.96), respectively. Immunohistochemical assay indicated that of the 81 cancer tissue samples, 45 (55.6%) was FOLR1 protein positive. FOLR1 protein positive expression rate in FIGO stage Ⅲ/Ⅳ was significant higher than in the stage Ⅰ/Ⅱ with statistical difference (P<0.05). The progression free survival (PFS) was significant different between FOLR1 high and low expression group (HR=2.48, 95%CI:1.1-5.58, P=0.023). However, the overall survival (OS) was not statistical different between the two groups (HR=1.34, 95%CI:0.84-2.15, P=0.22). Conclusion: FOLR1 was up-regulated in both serum and cancer tissue of cervical squamous cell carcinoma which may act as diagnostic and prognostic maker for cervical squamous cell cancer.
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来源期刊
Pteridines
Pteridines 生物-生化与分子生物学
CiteScore
1.20
自引率
25.00%
发文量
6
审稿时长
>12 weeks
期刊介绍: Pteridines is an open acess international quarterly journal dealing with all aspects of pteridine research. Pteridines are heterocyclic fused ring compounds involved in a wide range of biological functions from the color on butterfly wings to cofactors in enzyme catalysis to essential vitamins. Of the pteridines, 5,6,7,8-tetrahydrobiopterin is the necessary cofactor of several aromatic amino acid monoxygenases, the nitric oxide synthases and glyceryl ether monoxygenase (GEMO). Neopterin plays an essential role in the immune system and is an important biomarker in laboratory medicine for diseases such as HIV, cardiovascular disease, malignant tumors, among others. Topics: -Neopterin, dihydroneopterin, monapterin- Biopterin, tetrahydrobiopterin- Folates, antifolates, riboflavin- Phenylalanine, tyrosine, phenylketonuria, serotonin, adrenalin, noradrenalin, L-DOPA, dopamine, related biogenic amines- Phenylalanine hydroxylase, tyrosine hydroxylase, tryptophan hydroxylase, nitric oxide synthases (iNOS), alkylglycerol monooxygenase (AGMO), dihydropterin reductase, sepiapterin reductase- Homocysteine, mediators of inflammation, redox systems, iron.
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