国际肿瘤学杂志 ›› 2015, Vol. 42 ›› Issue (4): 255-258.doi: 10.3760/cma.j.issn.1673-422X.2015.04.005

• 论著 • 上一篇    下一篇

c-myc和CD24在结直肠癌的表达及意义

  

  1. 264200  青岛大学医学院附属威海医院消化内科(陈文军、董崇海);青岛大学医学院附属医院消化内科(田字彬)
  • 出版日期:2015-04-08 发布日期:2015-04-22
  • 通讯作者: 陈文军,Email: chwhju@163.com

Expression and significance of c-myc and CD24 in colorectal cancer

  1. Department of Gastroenterology, Weihai Affiliated Hospital of Medical College of Qingdao University, Weihai 264200, China  
  • Online:2015-04-08 Published:2015-04-22
  • Contact: Chen Wenjun, Email:chwhju@163.com

摘要: 目的检测cmyc和CD24在结直肠癌、息肉及正常黏膜中的表达,探讨c-myc和CD24在结直肠癌发生中的作用以及二者之间的关系。方法采用免疫组织化学法对60例结直肠癌、45例大肠腺瘤性息肉、15例大肠增生性息肉、30例正常结直肠黏膜石蜡切片进行cmyc和CD24表达的检测。结果cmyc阳性表达率在结直肠癌中为73.3%,明显高于大肠腺瘤性息肉44.4%(χ2=9.016 8,P<0.01)、大肠增生性息肉13.3%(χ2=18.215 9,P<0.01)和正常黏膜组织6.7%(χ2=35.573 1,P<0.01);CD24阳性表达率在结直肠癌中为76.7%,明显高于大肠增生性息肉6.7%(χ2=25.133 0,P<0.01)、正常黏膜组织3.3%(χ2=43.107 4,P<0.01)。cmyc与结直肠癌的肿瘤部位(χ2=8.352 3, P<0.01)、淋巴结转移(χ2=4.275 1, P<0.05)、分化程度(χ2=4.115 3, P<0.05)和分期(χ2=5.739 9, P<0.05)有相关性;CD24与肿瘤大小(χ2=9.333 6,P<0.01)、淋巴结转移(χ2=7.693 0,P<0.01)、分化程度(χ2=5.870 0, P<0.05)和分期(χ2=4.498 7, P<0.05)有相关性。结直肠癌组织中CD24与cmyc 表达呈正相关(χ2=10.824 9,r=0.39,P<0.05)。结论cmyc与CD24在结直肠癌中高表达,且与一些临床病理特征有关。在结直肠癌的发生、进展、转移过程中,cmyc很可能充当了CD24信号通路的下游靶基因,受CD24调控。

关键词: 结直肠肿瘤, 免疫组织化学, 基因, myc, CD24

Abstract: 【Abstract】ObjectiveTo determine the expression of cmyc and CD24 in colorectal carcinoma, colorectal polyp and normal mucosa, and to explore the role and correlation of them  in the carcinogenesis of colorectal carcinoma. MethodsThe expression of cmyc and CD24 in colorectal carcinoma (n=60), colorectal adenomatous polyp (n=45), colorectal hyperplastic polyp (n=15) and the adjacent noncancerous tissue (n=30) was observed by immunohistochemical assay. ResultsThe positive rate of cmyc in colorectal carcinoma were 73.3%, significantly higher than that in colorectal adenomatous polyp 44.4% (χ2=9.016 8, P<0.01), colorectal hyperplastic polyp 13.3% (χ2=18.215 9, P<0.01) and adjacent noncancerous tissue 6.7% (χ2=25.133 0, P<0.01); the positive rate of CD24 in colorectal carcinoma was 76.7%, significantly higher than that in colorectal hyperplastic polyp 6.7% (χ2=25.133 0, P<0.01) and adjacent noncancerous tissue 3.3% (χ2=43.107 4, P<0.01). cmyc expression in colon cancer was significantly correlated with cancer site (χ2=8.352 3, P<0.01), lymph node metastasis (χ2=4.275 1, P<0.05), differentiation (χ2=4.115 3, P<0.05) and TNM stage (χ2=5.739 9, P<0.05). CD24 expression in colon cancer was significantly correlated with cancer size (χ2=9.333 6, P<0.01), lymph node metastasis (χ2=7.693 0, P<0.01), differentiation (χ2=5.870 0, P<0.05) and TNM stage (χ2=4.498 7, P<0.05). There was a positive correlation relationship between CD24 and cmyc in colorectal carcinoma tissue (χ2=10.824 9, r=0.39, P<0.05).ConclusionThe expression of cmyc and CD24 are high in colorectal cancer, having a significant correlation with some of the clinicaopathological features. cmyc is likely to act as a downstream target gene of CD24 signaling pathway, whose expression is probably regulated by CD24 in colorectal carcinoma tissue.

Key words: Colorectal neoplasms, Immunohistochemistry, Genes, myc, CD24