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nm23-H1和PTEN蛋白与肝癌侵袭进展关系的研究 被引量:4

The Study about nm23-H1 and PTEN Protein in the Development of Primary Human Hepatocellular Carcinoma
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摘要 为研究原发性肝细胞性肝癌中nm23-H1和PTEN的表达状况,并分析两者的临床意义,本研究选取顺德第一人民医院2005年1月至2008年12月原发性肝细胞性肝癌手术患者蜡块标本68例,按Edmondson标准进行组织学分级,68例原发性肝细胞性肝癌组织为对照组,5例正常肝组织作为参照组。通过采取免疫组化S-P实验法测定两组标本nm23-H1、PTEN的表达。结果显示,nm23-H1蛋白在HCC、正常肝组织中的阳性表达率分别是30.88%(21168)、86.67%(13/15),nm23-H1在HCC中的表达低于正常肝组织(χ^2=15.813,p〈0.05)。同时,根据实验分析可见,PTEN在正常肝组织、肝癌组织中的阳性率分别为93.33%(14/15)、60.29%(41/68),且PTEN在HCC中的表达低于正常肝组织(χ^2=6.001,p〈0.05),两者均与肿瘤的分化程度和转移相关。本研究表明PTEN、nm23-H1与HCC侵袭性强弱和是否发生转移有一定的相关性。 In order to study the expression ofnm23-H1 and PTEN in primary hepatocellular carcinoma, and to analyze the clinical significance of the two, this study selected 68 patients with primary hepatocellular carcinoma from January 2005 to December 2008 who were enrolled in the Shunde First People's Hospital. The specimens were classified according to Edmondson criteria. 68 cases of primary hepatocellular carcinoma were selected as control group and 5 cases of normal liver tissue as reference group. The expression ofnm23-H1 and PTEN in the two groups was determined by immunohistochemical S-P assay. The results showed that the positive expression rates ofnm23-H1 protein in HCC and normal liver tissues were 30.88% (21/68) and 86.67% (13/15) respectively. The expression of nm23-H1 in HCC was lower than that in normal liver tissues (χ^2= 15.813, p〈0.05). Meanwhile, according to experimental analysis, the positive rates of PTEN in normal liver tissues and liver cancer tissues were 93.33% (14/15) and 60.29% (41/68), respectively. The expression of PTEN in HCC was lower than that of normal liver tissue (χ^2=6.001, p〈0.05), both of which were related to tumor differentiation and metastasis. The result showed that PTEN, nm23-H1 and HCC had a certain correlation with the strength of invasive and metastasis.
作者 王晓蔚 康凯夫 张鑫 Wang Xiaowei;Kang Kaifu;Zhang Xin(Yuncheng Vocational Nursing College,Yuncheng,044000;Shunde Hospital of Southern Medical University,Foshan,528300)
出处 《基因组学与应用生物学》 CAS CSCD 北大核心 2018年第11期4949-4954,共6页 Genomics and Applied Biology
基金 广东省社会发展领域科技计划项目(No.200883113)资助
关键词 原发性肝癌 NM23-H1 PTEN 免疫组化 nm23-H1 PTEN HCC Immunhistochemistry
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  • 1Chung MJ, Jung SH, Lee BJ, et al. Inactivation of the PTEN gene protein product is associated with the invasiveness and metastasis, but not angiogenesis, of breast cancer[J]. Pathol Int,2004,54(1):10-15. 被引量:1
  • 2Iizuka N, Oka M, Noma T, et al. Nm23H1 and nm23H2 messenger RNA abundance in human hepatocellular carcinoma[J]. Cancer Res, 1995,55(3):652-657. 被引量:1
  • 3Gazzeri S, Brambilla E, Negoescu A, et al. Overexpression of nucleoside diphosphate/kinase A/nm23H1 protein in human lung tumors: association with tumor progression in squamous carcinoma[J]. Lab Invest, 1996,74(1):158-167. 被引量:1
  • 4Lee CS, Redshaw A, Boag G, et al. Nm23H1 protein immunoreactivity in laryngeal carcinoma[J]. Cancer, 1996,77(11): 2246-2250. 被引量:1
  • 5Marone M, Scambia G, Ferrandina G, et al. Nm23 expression in endometrial and cervical cancer:inverse correlation with lymph node involvement and myometrial invasion[J]. Br J Cancer, 1996,74(7):1063-1068. 被引量:1
  • 6Fujii K, Yasui W, Shimamoto F, et al.Immunohistochemical analysis of nm23 gene product in human gallbladder carcinomas[J]. Virchows Arch, 1995,426(4):355-359. 被引量:1
  • 7杨竹林 李永国.胆道恶性肿瘤nm23基因蛋白表达及其意义[J].中华实验外科杂志,1995,9(5):361-361. 被引量:1
  • 8Bresalier RS,Ho SB,Schoeppner HL, et al. Enhanced sialylation of mucin associated carbohydrate structures in human colon cancer metastasis[J]. Gastroenterology,1996,110(5):1354-1367. 被引量:1
  • 9Besson A, Robbins SM, Yong VW. PTEN/MMAC1 mutations in signal transduetion and tumorigenesis[J]. Eur J Biochem, 1999,263:605-611. 被引量:1
  • 10Xue-fei Yang Yan Xin Li-li Mao.CLINICOPATHOLOGICAL SIGNIFICANCE OF PTEN AND CASPASE-3 EXPRESSIONS IN BREAST CANCER[J].Chinese Medical Sciences Journal,2008,23(2):95-102. 被引量:6

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