期刊文献+

中期因子转录物及其蛋白在肝细胞癌中的定位与表达研究 被引量:7

Expression and localization of midkine in hepatocellular carcinoma
原文传递
导出
摘要 目的了解中期因子 (Midkine,MK)转录物及其蛋白产物在肝细胞癌 (hepatocellularcarci noma ,HCC)中的定位情况与表达特点。方法应用原位杂交、免疫组织化学染色等方法对 33例人HCC组织、10例良性肝肿瘤组织及其配对瘤旁肝组织进行了MKmRNA及蛋白的定位与表达研究。结果免疫组织化学结果与原位杂交结果具有一致性 (χ2 =0 5 0 0 ,P >0 0 5 )。MK在HCC组织中呈高表达。MKmRNA及蛋白的阳性信号聚集于HCC细胞质。在HCC细胞外组织中亦有MK表达 ,尤以血管密集处明显。HCCMK表达率与肝癌组织学类型、分级等临床病理学特点无相关性。结论HCC在mRNA和蛋白水平上表达MK增加 。 ObjectiveTo investigate the expression and localization of midkine (MK) in human hepatocellular carcinoma. MethodsIn situ hybridization and immunohistochemical analysis for MK were performed on samples of both tumor tissues and paratumor tissues from HCC and benign liver tumors. ResultsThe distribution and localization of the MK transcripts′ signals determined by in situ hybridization were similar to those obtained by immunohistochemical analysis. Most HCC tissues showed enhanced positive reaction within cytoplasm to both MK probe and MK immunostaining. There was no significant difference in clinicopathological parameters between MK negative and positive cases of HCC. ConclusionsHuman hepatocellular carcinoma overexpresses MK at the mRNA and protein level.
出处 《中华普通外科杂志》 CSCD 北大核心 2002年第4期220-222,共3页 Chinese Journal of General Surgery
基金 上海市医学发展基金资助项目 ( 99ZDII0 0 1)
关键词 生物因子 原位杂交 免疫组织化学 肝细胞癌 中期因子转录物 蛋白定位 蛋白表达 Liver neoplasms Biological factors In situ hybridization Immunohistochemistry
  • 相关文献

参考文献1

二级参考文献2

  • 1Muramatsu H,J Bio Chem,1996年,119卷,6期,1171页
  • 2Fu C,Gene,1994年,146卷,311页

共引文献26

同被引文献57

  • 1张青云,杨敏,王雅明,徐建军.细胞因子Midkine融合蛋白的表达及其单克隆抗体的制备与应用[J].细胞与分子免疫学杂志,2005,21(5):605-608. 被引量:3
  • 2Ying-Jia Ren,Qing-Yun Zhang.Expression of midkine and its clinical significance in esophageal squamous cell carcinoma[J].World Journal of Gastroenterology,2006,12(13):2006-2010. 被引量:14
  • 3原丹丹,李福琴,董春花,刘倩.中期因子在卵巢上皮性肿瘤中的表达及临床意义[J].哈尔滨医科大学学报,2006,40(6):464-466. 被引量:8
  • 4Muramaki M,Miyake H,Hara I,et al.Introduction of midkine gene into human bladder cancer cells enhances their malignant phenotype but increases their sensitivity to antiangiogenic therapy[J].Clin Cancer Res,2003,9(14):5152-5160.
  • 5Mashour GA,Ratner N,Khan GA,et al.The angiogenic factor midkine is aberrantly expressed in NF1-deficient Schwann cells and is a mitogen forneurofibroma-derived cells[J].Oncogene,2001,20(1):97-105.
  • 6Muramaki M,Miyake H,Hara I,et al.Introduction of midkine gene into human bladder cancer cells enhances their malignant phenotype but increases theirsensitivity to antiangiogenic therapy[J].Clin Cancer Res,2003,9(14):5152-60.
  • 7DiSaia P J, Creasrnan W T. Clinical gynecologic oncokgy [ J ]. Sixth Edition Health Science Asia Elsevier Sci,2002,377.
  • 8Kadomatsu K, Muramatsu T. Midkine and pleiotrophin in neural development and cancer[J]. Cancer Lett,2004,204(2):127- 143.
  • 9Dai L, Xu D, Yao X, et al. Conformational determinants of the intraceltular localization of midkine[J]. Elsevier Publiser(Biochem. Res. Comman. ) ,2005,330(1) :310 - 317.
  • 10Aziz S, Kuperstein G, Rosen B, et al. A genetic epidemiological study of primary fallopian tube carcincma[ J ]. Gynecol Oncol, 2001,80 ( 3 ) : 341.

引证文献7

二级引证文献7

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