期刊文献+

LMW-PTP在子宫颈鳞癌中的表达及其临床意义 被引量:1

Expression of low molecular weight protein tyrosine phosphatase in cervical carcinoma and its significance
暂未订购
导出
摘要 目的探讨低分子量酪氨酸磷酸酶(LMW—PTP)在子宫颈鳞癌中的表达及其临床意义。方法采用RT—PCR及免疫组化法分析HaCaT、C33A、SiHa和CaSki细胞系中LMW,PTP的表达情况。免疫组织化学法检测正常宫颈患者19例,宫颈上皮内瘤变(CIN)I期患者18例、CINⅡ~Ⅲ患者46例和宫颈鳞癌患者76例的组织切片中LMW—PTP的表达。结果LMW—PTPmRNA及蛋白在C33A、SiHa及CaSki宫颈癌细胞系中表达明显高于人永生化正常表皮细胞系HaCaT;临床组织样本中,正常宫颈上皮LMW—PTP几乎不表达,在正常宫颈上皮到CIN继而发展成宫颈癌的进展过程中LMW—PTP的表达逐渐升高,差异有统计学意义(P〈0.05);低分化宫颈癌组织中LMW—PTP表达高于中分化组织(P=0.025),中分化宫颈癌组织中LMW—PTP的表达高于高分化组织(P=0.045);宫颈癌组织中LMW—PTP蛋白的表达与组织学分级程度和是否有淋巴结转移密切相关(P〈0.05)。结论LMW—PTP在宫颈癌的进展过程中起重要作用,且与组织分化程度和是否有淋巴转移密切相关,提示LMW—PTP的表达有助于判断宫颈癌患者的预后。 Objective To detect the expression of low molecular weight protein tyrosine phosphatase (LMW-PTP) proteins and its clinical significance in cervical cancer. Methods The expressions of LMW-PTP were determined by RT-PCR and immunohistochernieal assay in HaCaT, C33A, SiHa and CaSki. A series of samples, including 19 cases of normal cervical tissues, 18 cases of cervical intracpithelial neoplasia I phase, 46 cases of cervical intraepithelial neoplasia lI or m phase, 76 cases of squamous cell carcinoma (SCC) , were used to examine LMW-PTP immunohistochemical staining and statistical analysis. Results RT-PCR and Western blot results showed that expression of LMW-PTP in C33A, SiHa and CaSki were higher than expression of LMW-TFP in HaCaT. The results showed that LMW-PTP was barely observed in the normal cervical epithelial cells. With the progression of normal cervical epithelial cells to CIN and cervical cancer, the expression levels of LMW-PTP were increased. There was significantly difference for LMW-PTP expression among normal cervical tissues, CIN, cervical cancer (P 〈 0.05 ). 20 The expression of LMW-PTP in poorly differentiated cervical cancer was higher than expression of LMW-PTP in moderately differentiated cervical cancer which was higher expression of LMW-PTP than high differentiation of cerwith the progression of cervical carcinogenesis and development of cervical cancer. In addition, the association LMW-PTP with lymph node metastasis and histological grade of SCC suggests that LMW-PTP can be a potential therapeutic target of SCC patients.
出处 《安徽医科大学学报》 CAS 北大核心 2013年第12期1522-1526,共5页 Acta Universitatis Medicinalis Anhui
基金 国家自然科学基金(编号:81001168) 安徽省科技攻关计划项目(编号:08010302101)
关键词 宫颈癌 子宫上皮内瘤变 低分子量酪氨酸磷酸酶 淋巴结转移 cancer of cervix cervical intraepithelial neoplasia LMW-PTP lymph node metastasis
  • 相关文献

参考文献2

二级参考文献14

  • 1陈玲,贺慧颖,李红梅,由江峰,衡万杰,李燕,方伟岗.ERK1/2及p38通路调节P2Y受体介导的前列腺癌细胞体外侵袭[J].中华医学杂志,2005,85(2):111-114. 被引量:3
  • 2佟明,艾军魁,袁亦明,殷毅,周利群,辛殿旗,李鸣,那彦群.SRD5A2基因A49T多态性与前列腺癌风险性关系的研究[J].中华医学杂志,2005,85(19):1319-1321. 被引量:2
  • 3廖晖,陈安民,郭风劲,李锋,罗政强,宋登新,陈超.不同骨转移潜能人前列腺癌细胞亚株的筛选[J].中国癌症杂志,2007,17(3):231-235. 被引量:5
  • 4Yonou H, Yokose T, Kamijo T, et al. Establishment of a novel species-and tissue-specific metastasis model of human prostate in humanized no-obese diabetic/severe combined immunodeficient mice engrafted with human adult lung and bone. Cancer Res ,2001,61:2177-2182.
  • 5Letizia TM, Chiarugi P, Cirri P,et al. β-Catenin interacts with low-molecular-weight protein tyrosine phosphatase leading to cadherin-mediated cell-cell adhesion increase. Cancer Res, 2002, 62:6489-6499.
  • 6Taguchi A, Blood DC, del Toro G, et al. Blockage of RAGE- amphoterin signalling suppresses tumor growth and metastasis. Nature, 2000, 405:354-360.
  • 7Oue N, Aung PP, Mitani Y, et al. Genes involved in invasion and metastasis of gastric cancer identified by array-based hybridization and serial analysis of gene expression. Ontology, 2005, 69 Suppl 1:17-22.
  • 8Sasahira T, Akama Y, Fujii K, et al. Expression of receptor for advanced glycation end products and HMGB1/amphoterin in colorectal adenomas. Virchows Arch, 2005, 446:411-415.
  • 9Rauvala H, Huttunen HJ, Fages C, et al. Heparin-binding proteins HB-GAM (pleiotrophin) and amphoterin in the regulation of cell mobility. Matrix Biol,2000,19 :377-387.
  • 10Kuniyasu H, Chihara Y, Kondo H, et al. Differential effects between amphoterin and advanced glycation end products on colon cancer cell. Int J Cancer, 2003, 104:722-727.

共引文献30

同被引文献15

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部