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食管癌组织中肝素酶mRNA的表达 被引量:2

Relation between heparanase mRNA expression and metastasis of esopha-geal carcinoma
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摘要 目的:探讨肝素酶mRNA表达与食管癌转移的关系。方法:采用原位杂交技术检测了54例食管鳞癌、癌旁组织及其正常食管组织中肝素酶mRNA的表达。结果:21例有淋巴结转移的食管鳞癌癌组织、癌旁及正常组织中肝素酶mRNA阳性表达率分别为100%(21/21)、66.7%(14/21)和0%(0/21)。而在无淋巴结转移的33例食管鳞癌癌组织、癌旁及正常食管组织中肝素酶mRNA阳性表达率分别为30.3%(10/33)、24.2%(8/33)和0%(0/33)。2组癌组织、癌旁组织肝素酶mRNA阳性表达率差异有统计学意义(P<0.01)。结论:肝素酶mRNA表达与食管鳞癌转移有一定关系。 Aim :To investigate the relation between the mRNA expression of heparanase and the metastasis of esophageal carcinoma. Methods: The expression of heparanase mRNA in 54 cases esophageal cancer including cancerous tissues, mucosa adjacent to cancer,and normal mucosa was detected by in situ hybridization. Results: The positive rates of heparanase mRNA in cancerous tissues, mucosa adjacent to cancer, and normal tissues of cases with lymph node metastasis were 100% (21/21) , 66. 7% ( 14/21 ) , and 0% , respectirely, and the positive rates of heparanase mRNA in cancerous tissues, mucosa adjacent to cancer, and normal tissues of cases without lymph node metastasis were 30. 3% (10/33) , 24. 2% (8/33) and 0% , respectirely. There was significant difference between esophageal carcinoma with lymph node metastasis and esophageal carcinoma without lymph node metastasis (P < 0. 01). Conclusion : The results suggest the expression of heparanase gene may be related to the metastasis of esophageal carcinoma.
出处 《郑州大学学报(医学版)》 CAS 北大核心 2004年第2期179-181,共3页 Journal of Zhengzhou University(Medical Sciences)
基金 河南省自然科学基金资助项目 0311643700 河南省高校青年骨干教师资助项目 "十五""211工程"重点学科建设项目 教重办(2002)第2号
关键词 食管肿瘤 肝素酶 esophageal neoplasm carcinoma heparanase
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  • 1王伯沄 陆良勇 吴惠茜 等.原位核酸分子杂交技术[A].见:王伯法等主编.病理学技术[C].北京:人民卫生出版社,2000.565-594.
  • 2Vlodavsky I, Friemann Y, Elkin M, et al. Mammalian heparanase: gene cloning, expression and function in tumor progression and metastasis. Nat Med, 1999,5(7) :793.
  • 3Toyoshima M, Nakajima M. Human heparanase. J Bio Chem, 1999,274(34): 24 153.
  • 4Hulett MD, Hornby JR, Ohms SJ, et al. Identification of active-site residues of the pro-metastatic endoglycosidase heparanase. Biochemistry, 2000,39(51 ) :15 659.
  • 5Vaday GG, Lider O. Extracellular matrix moieties, cytokines, and enzymes: dynamic effects on immune cell behavior and inflammation. J Leuk Biol, 2000,67(2):149.
  • 6Nakajima M, Irimura T, Di Ferrante D, et al. Heparan sulfate degradation: relation to tumor in vasion and metastatic properties of mouse B16 melanoma sublines. Science, 1983,220(4 597) :611.
  • 7Hulett MD, Freeman C, Hamdorf BJ, et al. Cloning of mammalian heparanase, an important enzyme in tumor invasion and metastasis. Nat Med, 1999,5(7) :803.
  • 8Miao HQ, Omitz DM, Aingorn E, et al. Modulation of fibroblast growth factor-2 receptor binding, dimerization, signalling, and angio-genic activity by synthetic heparin-mimiclig polyanionic compound. J Clin Invest, 1997;99(7):1 565.
  • 9Ikuta M, Podyma KA, Maruyama K, et al. Expression of heparanase in oral cancer cell lines and oral cancer tissues.Oral Oncol, 2001, 37(2):177.

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  • 1Tsuchida S,Sato K.Glutathione transferase and cancer[J].Crit Rev Biochem Mol Biol,1992,27(4-5):337-384.
  • 2Kodate C,Fukushi A,Nareta T,et al.Human placental form of glutathione S-transferase (GST-π) as a new immunochemical marker for human colonic carcinoma[J].Jpn J Cancer Res,1986,77(3):226-229.
  • 3Shimizu K,Toriyama F,Zhang HM,et al.The expression of placental-type glutathione S-transferase (GST-pi) in human cutaneous carcinoma in situ,that is,actinic keratosis and Bowen's disease,compared with normal human skin[J].Carcinogenesis.1995,16(10):2327-2330.
  • 4Lim JL,Stern RS.High levels of ultraviolet B exposure increase the risk of non-melanoma skin cancer in psoralen and ultraviolet A-treated patients[J].J Invest Dermatol,2005,124(3):505-513.
  • 5Shiratori Y,Soma Y,Maruyama H,et al.Immumohistochemical detection of the placental form of glutathione S-transferase in dysplasia and neoplastic human aterine cervix lesion[J].Cancer Res,1987,47:6806-6809.
  • 6Shimizu K,Toriyama F,Yoshida H.The expression of placental-type glutathione (GST-π) in human cutaneous squamous cell carcinoma and normal human skin[J].Virchows Arch,1995,425(6):589-592.
  • 7Erb P,Ji J,Wern M,et al.Role of apoptosis in basal cell and squamous cell carcinoma formation[J].Immunol Lett.2005,100(1):68.
  • 8Tsuchida S, Sato K. Glutathione transferase and cancer [ J ]. Crit Rev Biochem Mol Biol, 1992,27 ( 4/5 ) :337.
  • 9Kodate C, Fukushi A, Narita T,et al. Human placental form of glutathione S-transferase (GST-π) as a new immunochemical marker for human colonic carcinoma [ J ]. Jpn J Cancer Res, 1986,77 ( 3 ) :226.
  • 10Shimizu K, Toriyama F, Zhang HM,et al. The expression of placental-type glutathione S-transferase (GST-pi) in human cutaneous carcinoma in situ, that is, actinic keratosis and Bowen's disease, compared with normal human skin [ J ]. Carcinogenesis, 1995,16 ( 10 ) : 2327.

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