期刊文献+

终端αGlcNAc糖基可能作为人胰腺癌细胞肿瘤标志物的初步研究 被引量:1

Terminal a-N-acetyiglucosamine residues possibly serve as one of the signs for humanpancreatic cancer
下载PDF
导出
摘要 目的探索终端为α-N-乙酰葡萄糖胺(αGlcNAc)糖基在胰腺癌组织和细胞中是否呈现特异高表达,从而确定终端αGlcNAc糖基是否可能作为胰腺癌的肿瘤标志物。方法利用特异性识别表位为终端αGlcNAc的商业化抗体(HIK1083),应用免疫组化方法,对11例胰腺癌患者和5例正常人胰腺组织进行检测。结果HIK1083抗体对11例胰腺癌组织/细胞均有明显的结合活性,而对正常胰腺组织和细胞无反应。结论终端αGlcNAc糖基可能作为胰腺癌细胞的肿瘤标志物,对胰腺癌的临床靶向治疗和诊断具有重要的研究价值。 Objective To explore the significant expression of terminal a-N-acetylglucosamine (aGlcNAc) residues in the tissues of pancreatic cancer and to determine if the residues could serve as one of the signs for pancreatic cancer. Methods The pancreatic tissues obtained from eleven pancreatic cancer patients and five normal subjects were analyzed by immunohistochemistry with commercial antibody HIK1083, which specially recognized the terminal aGlcNAc residues. Results The antibody, HIK1083, demonstrated a significant combination with the pancreatic tissues from cancer patients, but not in normal counterparts. Conclusion Terminal aGlcNAc residues might serve as the tumor marker for pancreatic cancers, and reflected a great value for implication in target treatment and diagnosis of pancreatic cancers.
出处 《中国急救复苏与灾害医学杂志》 2012年第11期1020-1023,共4页 China Journal of Emergency Resuscitation and Disaster Medicine
关键词 α-N-乙酰葡萄糖胺 胰腺癌 肿瘤标志物 a-N-acetylglucosamine Pancreatic cancer Tumor marker
  • 相关文献

参考文献17

  • 1Shimizu F, Nakayama J, Ishizone S, et reverse transcription-polymerase chain al. Usefulness of the real-time reaction assay targeted to a 1,4-N-acetylglucosaminyltransferase for the detection of gastric cancer. Lab Invest, 2003, 83(2):187-197.
  • 2Ishizone S, Yamauchi K, Kawa S, et al. Clinical utility of quantitative RT-PCR targeted to ct 1,4-N-acetylglucosaminyltransferase mRNA for detection of pancreatic cancer. Cancer Sei, 2006, 97(2):119-126.
  • 3Strasser R, Mucha J, Schwihla H,et al.Molecular cloning and characterization of cDNA coding for beta l,2N-acetylglucosaminyltransferase I (GlcNAc-TI) from Nicotlana tabacum. Glycobiology, 1999, 9(8):779-785.
  • 4Tan D'Agostaro AF, Bendiak B,et al.The human UDP-N- Acety-1 glucosaminect- 6-d-Mannoside-[3-1,2-N-Acety-lglucosaminy ltransferase II Gene (MGAT2).Eur J Biochem, 1995, 231(2):317-328.
  • 5Narasimhan S, Lee JW, Cheung RK, et al. Beta-l,4-mannosyl-glycoprotein beta-l,4-N-acetylglucosaminyltransferase III activity in human B and T lymphocyte lines and in tonsillar B and T lymphocytes. Biochemistry and cell biology, 1988, 66(8):889-900.
  • 6Broekhausen I, Mtiller G, Yang JM, et al. Control of glycoprotein synthesis. Characterization of (1-->4)-N-acetyl-beta-D-glucosaminyltransferases acting on the alpha-D-(1-->3)- and alpha-D-(1-->6)-linked arms of N-linked oligosaccharides. Carbohydr Res, 1992, 236:281-299.
  • 7Palcic MM, Ripka J, Kaur KJ,et al.Regulation of N-Acety- lglucosaminyl -transferase V Activity.J Biol Chem,1990,265(12): 6759-6769.
  • 8Demetriou M, Nabi IR, Coppolino M, et al. Reduced contact-inhibition and substratum adhesion in epithelial ceils expressing GlcNAc-transferase V.J Cell Biol, 1995, 130(2):383-392.
  • 9Brockhausen I, Carver JP, Schachter H. Control of glycoprotein synthesis. The use of oligosaccharide substrates and HPLC to study the sequential pathway for N-acetylglucosaminyltransferases I, II, III, IV, V, and VI in the biosynthesis of highly branched N-glycans by hen oviduct membranes . Biochemistry and cell biology, 1988, 66(10):1134-1151.
  • 10Nakayama J, Yeh JC, Misra AK, et al. Expression cloning of a human ct 1, 4-N-acetylglucosaminyltransferase that forms GlcNAc ct 1-4Ga113 R, a glycan specifically expressed in the gastric gland mucous cell-type mucin. Proc Nat1 Aead Sci U S A, 1999, 96(16):8991-8995.

二级参考文献33

  • 1陈翼,赵云辉,许乙凯,马黎明.联合运用MRI多种成像技术在胰腺肿块鉴别诊断中的价值[J].临床放射学杂志,2006,25(1):49-53. 被引量:12
  • 2朱志军,李林,张雅敏,郑虹,蒋文涛,张建军,高伟,淮明生,沈中阳.肝移植术后新发恶性肿瘤的诊治[J].中华肿瘤杂志,2007,29(3):237-238. 被引量:17
  • 3Jain A, Yee L, Nalesnik MA, et al. Comparative incidence of de novo nonlymphoid malignancies after liver transplantation under tacrolimus using surveillance epidemiologic end result date. Transplantation, 1998,66:1193-1200.
  • 4Penn I. Posttransplantation de novo tumors in liver allograft recipients. Liver Transpl Surg, 1996,2 (1) : 52-59.
  • 5Yao FY, Gautam M, Palese C, et al. De novo malignancies following liver transplantation: a case-control study with long-term follow-up. Clin Transplant, 2006,20 (5) : 617-623.
  • 6Sheil AG, Disney AP, Mathew TH, et al. Lymphoma incidence, cyclosporine, and the evolution and major impact of malignancy following organ transplantation. Transplant Proc, 1997,29: 825-827.
  • 7Benten D, Sterneck M, Panse J, et al. Low recurrence of preexisting extrahepatic malignancies after liver transplantation. Liver Transpl, 2008,14 (6): 789-798.
  • 8de Kroon L, Drent G, van den Berg AP, et al. Current health status of patients who have survived for more than 15 years after liver transplantation. Neth J Med, 2007,65 (7) : 252-258.
  • 9Dumortier J, Guillaud O, Adham M, et al. Negative impact of de novo malignancies rather than alcohol relapse on survival after liver transplantation for alcoholic cirrhosis: a retrospective analysis of 305 patients in a single center. Am J Gastroenterol, 2007, 102 (5): 1032-1041.
  • 10Aseni P, Vertemati M, De Carlis L, et al. De novo cancers and post-transplant lymphoproliferative disorder in adult liver transplantation. Pathol Int, 2006,56 (11) : 712-715.

共引文献12

同被引文献18

引证文献1

二级引证文献14

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