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本文引用的文献

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FGFR3 and P53 characterize alternative genetic pathways in the pathogenesis of urothelial cell carcinoma.FGFR3和P53是尿路上皮细胞癌发病机制中不同遗传途径的特征。
Cancer Res. 2004 Mar 15;64(6):1911-4. doi: 10.1158/0008-5472.can-03-2421.
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Primary carcinoma of the liver: a study of 100 cases among 48,900 necropsies.原发性肝癌:48900例尸检中的100例研究。
Cancer. 1954 May;7(3):462-503. doi: 10.1002/1097-0142(195405)7:3<462::aid-cncr2820070308>3.0.co;2-e.
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Down-regulation of growth arrest DNA damage-inducible gene 45beta expression is associated with human hepatocellular carcinoma.生长停滞DNA损伤诱导基因45β表达下调与人类肝细胞癌相关。
Am J Pathol. 2003 Jun;162(6):1961-74. doi: 10.1016/s0002-9440(10)64329-5.
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Cancer statistics, 2003.2003年癌症统计数据。
CA Cancer J Clin. 2003 Jan-Feb;53(1):5-26. doi: 10.3322/canjclin.53.1.5.
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Prognostic histologic indicators of curatively resected hepatocellular carcinomas: a multi-institutional analysis of 425 patients with definition of a histologic prognostic index.根治性切除肝细胞癌的预后组织学指标:425例患者的多机构分析及组织学预后指数的定义
Am J Surg Pathol. 2002 Jan;26(1):25-34. doi: 10.1097/00000478-200201000-00003.
6
The incidence of thanatophoric dysplasia mutations in FGFR3 gene is higher in low-grade or superficial bladder carcinomas.在低级别或浅表性膀胱癌中,FGFR3基因中致死性发育异常突变的发生率较高。
Cancer. 2001 Nov 15;92(10):2555-61. doi: 10.1002/1097-0142(20011115)92:10<2555::aid-cncr1607>3.0.co;2-m.
7
Analysis of FGFR3 gene mutations in multiple myeloma patients with t(4;14).伴有t(4;14)的多发性骨髓瘤患者FGFR3基因突变分析
Br J Haematol. 2001 Aug;114(2):362-4. doi: 10.1046/j.1365-2141.2001.02957.x.
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Expression profiling and identification of novel genes in hepatocellular carcinomas.肝细胞癌中新型基因的表达谱分析与鉴定
Oncogene. 2001 May 10;20(21):2704-12. doi: 10.1038/sj.onc.1204391.
9
Frequent FGFR3 mutations in papillary non-invasive bladder (pTa) tumors.乳头状非浸润性膀胱(pTa)肿瘤中频繁出现的成纤维细胞生长因子受体3(FGFR3)突变。
Am J Pathol. 2001 Jun;158(6):1955-9. doi: 10.1016/S0002-9440(10)64665-2.
10
Mutations in fibroblast growth factor receptor 2 and fibroblast growth factor receptor 3 genes associated with human gastric and colorectal cancers.与人类胃癌和结直肠癌相关的成纤维细胞生长因子受体2和成纤维细胞生长因子受体3基因的突变。
Cancer Res. 2001 May 1;61(9):3541-3.

成纤维细胞生长因子受体3在人肝细胞癌中的过表达。

Over-expression of fibroblast growth factor receptor 3 in human hepatocellular carcinoma.

作者信息

Qiu Wei-Hua, Zhou Bing-Sen, Chu Peiguo-G, Chen Wen-Gang, Chung Christopher, Shih Jennifer, Hwu Paul, Yeh Christopher, Lopez Richard, Yen Yun

机构信息

City of Hope National Medical Center, 1500 E. Duarte Road, Duarte, CA 91010, USA.

出版信息

World J Gastroenterol. 2005 Sep 14;11(34):5266-72. doi: 10.3748/wjg.v11.i34.5266.

DOI:10.3748/wjg.v11.i34.5266
PMID:16149130
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4622793/
Abstract

AIM

To describe the significant over-expression of fibroblast growth factor receptor 3 (FGFR3), which is a signal transduction and cell proliferation related gene in hepatocellular carcinoma (HCC).

METHODS

Following DNA microarray, Northern blot and quantitative real-time PCR were employed to confirm FGFR3 expression difference in HCC tissues and surrounding non-neoplastic liver tissue. FGFR3 expression levels were further determined by immunohistochemical study in 43 cases of HCC.

RESULTS

Northern blot results showed the significant over-expression of FGFR3 in HCC tissues, which was consistent with that from DNA microarray. Quantitative real-time PCR demonstrated that the mean ratio of FGFR3 mRNA to glyceraldehyde-3-phosphate dehydrogenase (GADPH) mRNA in HCC tissue was 0.250, whereas the ratio in non-neoplastic liver tissue was 0.014. Statistical analyses of 43 cases of HCC revealed that HCC scored higher than the matched non-neoplastic liver tissues. Examination of clinicopathological features revealed a strong correlation of over-expression of FGFR3 with poor tumor differentiation and high nuclear grade.

CONCLUSION

Over-expression of FGFR3 may play an important role in liver carcinogenesis. FGFR3 may be an ideal candidate as a molecular marker in the diagnosis of HCC and a potential therapeutic target.

摘要

目的

描述成纤维细胞生长因子受体3(FGFR3)在肝细胞癌(HCC)中的显著过表达,FGFR3是一种与信号转导和细胞增殖相关的基因。

方法

在DNA微阵列分析之后,采用Northern印迹法和定量实时PCR来确认FGFR3在HCC组织和周围非肿瘤性肝组织中的表达差异。通过免疫组织化学研究进一步测定43例HCC中FGFR3的表达水平。

结果

Northern印迹结果显示FGFR3在HCC组织中显著过表达,这与DNA微阵列分析结果一致。定量实时PCR表明,HCC组织中FGFR3 mRNA与甘油醛-3-磷酸脱氢酶(GADPH)mRNA的平均比值为0.250,而非肿瘤性肝组织中的比值为0.014。对43例HCC的统计分析显示,HCC的得分高于配对的非肿瘤性肝组织。对临床病理特征的检查显示,FGFR3的过表达与肿瘤分化差和核分级高密切相关。

结论

FGFR3的过表达可能在肝癌发生中起重要作用。FGFR3可能是HCC诊断中理想的分子标志物候选物和潜在的治疗靶点。