期刊文献+

CYP39A1基因在肝癌组织中的表达及临床意义 被引量:1

Expression of CYP39A1 in hepatocellular carcinoma tissue and its clinical significance
下载PDF
导出
摘要 目的检测人肝癌组织中CYP39A1基因的表达,探讨其与人肝癌临床病理特征的关系。方法应用免疫组化SP法检测32例肝癌组织及其相应的癌旁正常组织中CYP39A1基因的表达。结果 32例肝癌组织中CYP39A1基因阳性及强阳性表达率(25.00%)显著低于其相应的癌旁正常组织(93.75%),差异具有统计学意义(P<0.01)。32例肝癌组织中,CYP39A1基因表达程度与患者的性别、淋巴结转移、远处转移、T分期(T1期+T2期,T3期+T4期)无关(P>0.05),与患者年龄及肿瘤分化程度有关(P<0.05)。结论 CYP39A1基因在肝癌的发生、发展中起着重要作用,可能成为肝癌靶向治疗的一个新靶点。 Objective To detect the expression of CYP39A1 in human hepatocellular carcinoma( HCC),and to explore its relationship with clinical and pathological features of HCC. Methods The expression of CYP39A1 was detected by immunohistochemistry in 32 HCC specimens and their corresponding adjacent normal tissues. Results The rate of positive and strong positive expression of CYP39A1 in HCC tissue was significantly lower than that in adjacent normal tissue( 25. 00% vs 93. 75%,P〈 0. 01). The expression of CYP39A1 was correlated with age and poor differentiation( P 〈0. 05),but not correlated with gender,lymph node metastasis,distant metastasis and T stage( T3 + T4)( P 〈0. 05). Conclusion CYP39A1 gene plays an important role in the occurrence and development of HCC,and may be the novel treatment target of HCC.
出处 《胃肠病学和肝病学杂志》 CAS 2016年第8期865-867,共3页 Chinese Journal of Gastroenterology and Hepatology
关键词 肝癌 癌旁正常组织 CYP39A1基因 免疫组化 Hepatocellular carcinoma Adjacent normal tissue CYP39A1 gene Immunohistochemistry
  • 相关文献

参考文献6

  • 1王斌,李德远.细胞色素P450的结构与催化机理[J].有机化学,2009,29(4):658-662. 被引量:28
  • 2Huang YW, Jansen RA, Fabbri E, et al. Identification of candidate epigenetic biomarkers for ovarian cancer detection [J]. Oncol Rep, 2009, 22(4) : 853-861.
  • 3Khenjanta C, Thanan R, Jusakul A, et al. Association of cyp39al, runx2 and oxidized alpha-1 antitrypsin expression in relation to cholan- giocarcinoma progression [ J]. Asian Pac J Cancer Prev, 2014, 15(23): 10187-10192.
  • 4Li-Hawkins J, Lund EG, Bronson AD, et al. Expression cloning of an oxysterol 7alpha-hydroxylase selective for 24-hydroxycholesterol [J]. J Biol Chem, 2000, 275(22) : 16543-16549.
  • 5Uehiyama T, Kanno H, Ishitani K, et al. An SNP in CYP39A1 is as- sociated with severe neutropenia induced by docetaxel [ J]. Cancer Chemother Pharmacol, 2012, 69(6) : 1617-1624.
  • 6Melchardt T, Hufnagl C, Magnes T, et al. Cyp39al polymorphism is associated with toxicity during intensive induetion chemotherapy in pa- tients with advanced head and neck cancer [ J]. BMC Cancer, 2015, 15 : 725.

二级参考文献29

  • 1王斌,苏喜生,张声华.一氧化氮合酶的结构及其催化机理[J].有机化学,2005,25(3):342-345. 被引量:10
  • 2Denisov, I. G.; Makris, T. M.; Sligar, S. G. Chem. Rev. 2005, 105(6), 2253.
  • 3Masatomo, M.; Hiroshi, S.; Yoshitsugu, S.; Shumpei, A.; Hiroyasu, O.; Shingo, N. Proc. Natl. Acad. Sci. U. S. A. 2007, 104(28), 11591.
  • 4Ivan, J. D.; Brian, R. C.; Jonathan, J, W.; Jay, R. W.; Harry, B. G. Proc. Natl. Acad. Sci. U. S. A. 1999, 96(23), 12987.
  • 5Scott. E. E.; He, Y. A. Proc. Natl. Acad. Sci. U. S. A. 2003, 100(23), 13196.
  • 6Zhao, Y.-H.; White, M. A.; Muralidharaet, B. K.; Sun, L.; Halpert, J. R.; Stout, D. C. J. Biol. Chem. 2006, 281(9), 5973.
  • 7Muralidhara, B. K.; Negi, S.; Chin, C. C.; Braun, W.; Halpert, J. R. J. Biol. Chem. 2006, 281(12), 8051.
  • 8Pylypenko, 0.; Schlichting, I. Annu. Rev. Biochem. 2004, 73, 991.
  • 9Wade, R. C,; Winn, P. J.; Schlichting, I. J. Inorg. Biochem. 2004, 98(7), 1175.
  • 10Koshland, D. E. Angew. Chem.,Int. Ed. Engl. 1994, 33, 2375.

共引文献27

同被引文献12

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