期刊文献+

肿瘤标记物表达对A/B期结直肠癌患者预后的影响

Influence of expression of tumor markers on prognosis of patients with A/B-stage colorectal cancer
原文传递
导出
摘要 目的了解结直肠癌转移相关标记物过表达对A/B期患者预后的影响。方法收集2001至2002年65例结直肠癌的石蜡标本,用免疫组化染色检测CD44V6、MMP-2、COX-2、EGF、EGFR和VEGF的表达情况。比较阳性表达组和阴性表达组之间5年复发转移率的差异和多个肿瘤标记物过表达对预后的影响。结果A/B期结直肠癌中,CD44V6、EGF和EGFR蛋白阳性组的5年复发转移率分别为30.9%、38.1%和27.5%,显著高于阴性组的5年复发转移率8.3%、8.8%和11.8%(P=0.045、0.022和0.047);有3个以上指标阳性组的5年复发转移率高于0~2个指标阳性组,而5年生存率低于0~2指标阳性组,差异均有显著性(P=0.019和0.030)。结论CD44V6、EGF和EGFR蛋白过表达与Dukes A/B期患者高复发转移相关,肿瘤转移标记物高表达越多,复发转移的机率越高,5年生存率越低。 Objective To evaluate the relationship between tumor marker over-expression and prognosis of the colorectal cancer( CRC ) in Dukes A/B stage. Methods Paraffin-embedded specimens of 65 cases of CRC were collected to evaluate abnormal expression of CD44V6, MMP-2, COX-2, EGF, EGFR and VEGF using the method of immunhistochemistry(IHC). The differences of 5-year recurrence and metastasis rates between positive expression group and negative group and the differences of prognosis affected by multitude tumor markers overexpression in the eolorectal cancer were compared. Results In Dukes A/B stage, the 5-year recurrence rates were 30. 9% , 38. 1% and 27. 5% in the positive expression groups and was 8.3%, 8.8% and 11.8% in the negative groups of CD44V6, EGF and EGFR respectively. In Dukes A/B stage, the more the positive tumor markers, the higher the possibility of the 5-year recurrence rate and the lower the 5-year survival rate. Conclusions The tumor markers CD44V6, EGF and EGFR were the prognostic indicators of CRC in Dukes A/B stage. Moreover, In Dukes A/B stage, the more the positive tumor markers, the higher the possibility of the 5-year recurrence rate and the lower the 5-year survival rate.
出处 《中国肿瘤临床与康复》 2009年第1期25-27,共3页 Chinese Journal of Clinical Oncology and Rehabilitation
关键词 结直肠肿瘤 肿瘤标记物 免疫组织化学 Colorectal neoplasms Tumor marker Immunohistochemistry
  • 相关文献

参考文献7

二级参考文献39

  • 1梁英杰,凌启波.一种快速高敏感的免疫组织化学染色法—LSAB法[J].中华病理学杂志,1993,22(6):369-369. 被引量:71
  • 2蒋曹阳,郁宝铭,王瑞年.结直肠癌浸润转移机制的研究进展[J].肿瘤,1995,15(3):286-288. 被引量:2
  • 3[1] Liotta LA, Rao CN,Barsky SH.Invasion and extracellular matrix. Lab Invest,1983,49:636-639
  • 4[2] Pignatelli M,Vessdy CJ.Adhesion molecules:novel molecular tool s in tumor pathology.Hum Pathol,1994,25:849-896
  • 5[4] Aruffo A,Stamenkouic I,Melmick M,et al.CD44 is the principal c ell surface receptor for hyaluronate.Cell,1990,61:1303-1313
  • 6[5] Guo YJ,Lin GL,Wang XN,et al.Potential use of soluble CD44s in serum as indicator of tumor burden and metastasis in patients with gastric or co lon cancer.Cancer Res,1994,54:422
  • 7[7] Speiser P,Wanner C,Tempfer C,et al.CD44 is an independent prog nostic factor in early-stage cervical cancer.Int J Cancer,1997,74:185-188
  • 8[8] Mulder JM,Krayt PM,Sewnath M,et al.Colorectal cancer prognosis and expression of exon-v6-containing CD44 proteins.Lancet,1994,344:1470-157 2
  • 9[1]Senger DR, Galli SJ, Dvorak AM, et al.Tumor cells secrete a vascular permeability factor that promotes accumulation of ascites fluid [J]. Science, 1983; 219(4587)∶983
  • 10[2]Connolly DT, Heuvelman DM, Nelson R, et al.Tumor vascular permeability factor stimulates endothelial cell growth and angiogenesis [J]. J Clin Invest, 1989; 84(5)∶1470

共引文献45

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