期刊文献+

OY—TES-1在肿瘤组织中的表达及生物信息学分析 被引量:4

Expression of OY-TES-1 in tumor tissues and its bioinformatics analysis
下载PDF
导出
摘要 目的:了解OY-TES-1mRNA及其蛋白在肿瘤组织中的表达情况,初步探讨其结构与功能。方法:利用定量PCR和免疫组织化学技术检测肿瘤组织中OY—TES-1的表达,结合生物信息学技术分析其结构和功能。结果:肿瘤与瘤旁组织中目的基因mRNA的表达频率分别为61.95%和59.57%,其中肝细胞癌72.97%、脑膜瘤55.5s%、胶质瘤57.50%,肿瘤组织中该基因mRNA的表达量明显高于瘤旁组织。目的蛋白在胃癌的阳性率为25.00%,肝细胞癌40.00%,结肠癌46.67%,而瘤旁组织与肺癌均为阴性反应。生物信息学分析提示目的蛋白富含螺旋结构,具有一个信号肽、多种修饰位点及sp32结构域,存在较多T、B细胞表位且主要位于目的蛋白的羧基端。结论:OY-TES-1mRNA及其蛋白均可在肿瘤组织中表达,生物信息学分析结果提示该蛋白功能的多样性。 Objective: To explore gene expression characteristics of OY-TES-1 mRNA and protein level in tumor tissues, and predict its structure and function by bioinformatics analysis. Methods: Tumor tissues were tested to explore the expression of OY-TES-1 mRNA and protein by quantitative PCR and immunohistochemistry staining. The structure and function of OY TES-1 were predicted by bioinformatics techniques. Results: The expressive frequencies of OY-TES-1 mRNA in tumor and adjacent tumor tissues were 61.95% and 59.57% respectively, including 72. 97% in hepatocellular carcinoma, 55.56% in meningioma and 57.50% in glioma, and the expression level of OY-TES-1 mRNA in tumor tissues was higher than that in adjacent tumor tissues. The expressive rate of OY-TES-1 protein in tumor tissues was 25.00% in gastric carcinoma, 40. 00% in hepatocellular carcinoma, and 46.67% in colonma tissues, while adjacent tumor tissues and lung cancer showed negative. Bioinformatics method indicated that target protein was full of helices with a signal peptide, multitude modit'ication sites and sp32 domains. Immunogenicity of OY-TES-1 protein was found with many T cell epitopes and B cell epitopes, which mainly exist in carhoxyl terminus of the target protein. Conclusion: Both OY-TES-1 mRNA and protein could be found in tumor tissues, and the functional diversity of this protein can be predicted by bioinformatics techniques.
出处 《解剖学杂志》 CAS CSCD 北大核心 2009年第5期603-606,共4页 Chinese Journal of Anatomy
基金 国家自然科学基金(30360026,30760055) 广西科学基金(桂科自0728148)
关键词 精子蛋白32 基因表达 肿瘤 生物信息学分析 sperm protein 32 gene expression tumor bioinformatics analysis
  • 相关文献

同被引文献38

  • 1龙海霞,万瑾,王远强,朱波,倪兵,吴玉章,林治华.肿瘤抗原MAGE-A亚家族共同B细胞表位预测及分析[J].免疫学杂志,2009,25(5):572-576. 被引量:5
  • 2陈红松,张华刚,梅铭惠,费然,丛旭,覃理灵,魏来,陈慰峰.NY-ESO-1和MAGE-A3抗原肽诱导肝癌患者的免疫应答研究[J].免疫学杂志,2006,22(6):659-663. 被引量:4
  • 3Armstrong DK, Bundy B, Wenzel L et al. Intraperitoneal cisplatin and paclitaxel in orarian cancer [J]. N Engl J Med, 2006, 364 (1): 34.
  • 4Ono T, Kurashige T, Harada N et al. Identification of proacrosin binding protein sp32 precursor as a human cancer/testis antigen [J]. Proc Natl AcadSci USA, 2001, 98 (6): 3282.
  • 5Tammela J, Ucnaka A, Ono T et al. OY - TES - 1 expression and serum immuoreactivity in epithelial ovarian cancer [J]. Int J Oncol, 2006, 29 (4): 903.
  • 6Filipowicz W, Jaskiewicz L, Kolb FA et al. Post - transcriptional gene silencing by siRNAs and miRNAs [J] . Curr Opin Struct Biol, 2005, 15 (3) : 331.
  • 7Campbell TN, Choy FY. RNA interference: past, present and future [J].Curr Issues Mol Biol, 2005, 7 (1): 1.
  • 8Almofti MR, Harashima H, Shinohara Y et al. Cationic liposome - mediated gene delivery: biophysical study and mechanism of internalization [J]. Arch Biochem Biophys, 2003, 410 (2): 246.
  • 9Dykxhoorn DM, Novina CD, Sharp PA. Killing the messenger: short RNAs that silence gene expression [J]. Nat Rev Mol Cell Biol, 2003. 4 (6): 457.
  • 10Ono T, Kurashige T, Harada N, et al. Identification ofproacrosin binding protein sp32 precursor as a human cancer/testis antigen [J].Proe Natl Aead Sei USA, 2001, 98(6): 3282-3287.

引证文献4

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