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核仁磷酸蛋白/B23在肝细胞癌中的表达增加及其与临床病理参数的相关性

Increased expression of nucleophosmin/B23 in hepatocellular carcinoma and correlation with clinicopathological parameters.

作者信息

Yun J-P, Miao J, Chen G G, Tian Q-H, Zhang C-Q, Xiang J, Fu J, Lai P B S

机构信息

State Key Laboratory of Oncology in Southern China, Cancer Center, Sun Yat-Sen University, Guangzhou, China.

出版信息

Br J Cancer. 2007 Feb 12;96(3):477-84. doi: 10.1038/sj.bjc.6603574. Epub 2007 Jan 23.

DOI:10.1038/sj.bjc.6603574
PMID:17245342
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2360035/
Abstract

Nucleophosmin (NPM, B23, numatrin, NO38) is an abundant nucleolar phosphoprotein involved in multiple cellular functions. Previous evidence indicates that high-level expression of NPM causes uncontrolled cell growth and suggests that NPM may have oncogenic potential. In this study, we examined NPM expression in 103 paired cases of hepatocellular carcinoma (HCC), 12 cases of hepatic focal nodular hyperplasia, 17 cases of liver tissue adjacent to a hepatic haemangioma, and series of array tissues from normal human organs and malignancies using a monoclonal antibody against NPM and reverse transcription-PCR techniques, Western blot analysis, immunohistochemistry, and immunocytofluorescence. Our data indicated that NPM expression was significantly higher in HCC than in the non-malignant hepatocytes (P<0.001). Nucleophosmin was weakly expressed in hepatocytes from a 5-month-old embryo and in stationary hepatocytes of healthy adults. Moreover, enhanced expression of NPM in HCC correlated with the level of PCNA (R(2)=0.5639) and with the clinical prognostic parameters such as serum alpha fetal protein level, tumour pathological grading, and liver cirrhosis (P<0.05). Our results suggest that NPM may play an important role in the progression of tumorigenesis and that NPM may serve as a potential marker for HCC.

摘要

核磷蛋白(NPM,B23,核基质蛋白,NO38)是一种丰富的核仁磷蛋白,参与多种细胞功能。先前的证据表明,NPM的高水平表达会导致细胞生长失控,并提示NPM可能具有致癌潜力。在本研究中,我们使用抗NPM单克隆抗体以及逆转录 - PCR技术、蛋白质免疫印迹分析、免疫组织化学和免疫细胞荧光技术,检测了103对肝细胞癌(HCC)病例、12例肝局灶性结节性增生、17例肝血管瘤旁肝组织以及来自正常人体器官和恶性肿瘤的一系列组织芯片中NPM的表达情况。我们的数据表明,HCC中NPM的表达显著高于非恶性肝细胞(P<0.001)。核磷蛋白在5个月大胚胎的肝细胞以及健康成年人的静止肝细胞中表达较弱。此外,HCC中NPM表达的增强与PCNA水平(R(2)=0.5639)以及血清甲胎蛋白水平、肿瘤病理分级和肝硬化等临床预后参数相关(P<0.05)。我们的结果表明,NPM可能在肿瘤发生发展中起重要作用,并且NPM可能作为HCC的潜在标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5b8/2360035/9cf5cbc67b5c/6603574f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5b8/2360035/65ba7a839ab4/6603574f1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5b8/2360035/96b279b18932/6603574f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5b8/2360035/569250008f48/6603574f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5b8/2360035/a761ef0c5eec/6603574f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5b8/2360035/2f82ec30f7ff/6603574f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5b8/2360035/b81afde55abc/6603574f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5b8/2360035/9cf5cbc67b5c/6603574f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5b8/2360035/65ba7a839ab4/6603574f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5b8/2360035/31093354796c/6603574f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5b8/2360035/96b279b18932/6603574f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5b8/2360035/569250008f48/6603574f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5b8/2360035/a761ef0c5eec/6603574f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5b8/2360035/2f82ec30f7ff/6603574f6.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5b8/2360035/9cf5cbc67b5c/6603574f8.jpg

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