国际肿瘤学杂志 ›› 2016, Vol. 43 ›› Issue (5): 346-349.doi: 10.3760/cma.j.issn.1673422X.2016.05.007

• 论著 • 上一篇    下一篇

UHRF1和P53在结肠癌中的表达及临床意义

艾晓晴,贾喜花,王晓博,郑淑君,赵霞,张丙信   

  1. 071000 保定市第一中心医院肿瘤内科
  • 出版日期:2016-05-08 发布日期:2016-04-07
  • 通讯作者: 贾喜花 E-mail:15903126558@163.com

Expressions of UHRF1, P53 and their clinical significances in colon carcinoma

Ai Xiaoqing, Jia Xihua, Wang Xiaobo, Zheng Shujun, Zhao Xia, Zhang Bingxin   

  1. Department of Medical Oncology, Baoding First Central Hospital, Baoding 071000, China
  • Online:2016-05-08 Published:2016-04-07
  • Contact: Jia Xihua E-mail:15903126558@163.com

摘要: 目的探讨结肠癌组织中泛素样含PHD和环指域1(UHRF1)、P53蛋白的表达及其临床意义。方法采用免疫组织化学法检测70例结肠癌组织和30例癌旁正常组织中UHRF1、P53蛋白的表达情况,分析两者在结肠癌发生发展中的相关性,及其与结肠癌患者临床病理特征和预后的关系。结果UHRF1和P53在结肠癌癌组织中表达均明显高于癌旁正常组织(87.1%∶56.7%,χ2=11.366,P=0.001;64.3%∶6.7%,χ2=27.988,P=0.000),且两者在结肠癌中的表达呈正相关(r=0.248,P=0.038)。UHRF1、P53蛋白在结肠癌中的表达与肿瘤TNM分期(χ2=4.426,P=0.049;χ2=6.000,P=0.016)、浸润深度(χ2=12.553,P=0.002;χ2=4.904,P=0.036)密切相关,与患者年龄(χ2=0.473,P=0.494;χ2=0.090,P=0.799)、性别(χ2=2.297,P=0.166;χ2=0.512,P=0.617)、肿瘤大小(χ2=0.638,P=0.481;χ2=2.392,P=0.215)、分化程度(χ2=2.088,P=0.352;χ2=0.303,P=0.859)无关。KaplanMeier曲线提示,UHRF1、P53均阳性表达患者的中位生存时间为21.83个月,较单独UHRF1阳性表达者(24.49个月)短(Z=-0.624,P=0.533),前两者中位生存时间明显较UHRF1阴性表达者(37.33个月)短(Z=-2.856,P=0.004;Z=-2.694,P=0.007)。结论UHRF1、P53在结肠癌中均呈高表达,二者与结肠癌的发生发展密切相关,其表达强度可以作为患者预后的重要指标。

关键词: 结肠肿瘤, 肿瘤抑制蛋白质p53, 泛素样含PHD和环指域1

Abstract: ObjectiveTo investigate the expression levels and clinical significances of ubiquitinlike with PHD and ring finger domains 1 (UHRF1) and P53 in colon carcinoma. MethodsThe expressions of UHRF1 and P53 in 70 colon cancer tissues and 30 normal colon ones were detected by means of immunohistochemistry to analyze the correlation of these two proteins in the occurrence and development of colon carcinoma, and the relationship between their expressions and clinicopathological factors as well as prognosis was discussed. ResultsThe expression levels of UHRF1 and P53 in cancer tissues were significantly higher than those of canceradjacent tissues (87.1% vs. 56.7%, χ2=11.366, P=0.001; 64.3% vs. 6.7%, χ2=27.988, P=0.000) and showed a positive correlation between the two proteins (r=0.248, P=0.038). Both UHRF1 and P53 were associated with TNM stages (χ2=4.426, P=0.049; χ2=6.000, P=0.016) and the depth of invasion (χ2=12.553, P=0.002; χ2=4.904, P=0.036). However, they were irrelevant with the age (χ2=0.473, P=0.494; χ2=0.090, P=0.799) and gender (χ2=2.297, P=0.166; χ2=0.512, P=0.617) of patients, as well as the size (χ2=0.638, P=0.481; χ2=2.392, P=0.215) and histological grading of tumors (χ2=2.088, P=0.352; χ2=0.303, P=0.859). KaplanMeier analysis showed that the median survival time of patients with UHRF1, P53 positive expression was 21.83 months that was lower than patients with UHRF1 positive expression of 24.49 months (Z=-0.624, P=0.533). Both former of which was distinctly lower than that of negative ones of 37.33 months (Z=-2.856, P=0.004; Z=-2.694, P=0.007). ConclusionBoth UHRF1 and P53 are highly expressed in colon cancer tissues, which imply that UHRF1 and P53 may be strongly related with colon cancer development and can be a predictor for colon cancer prognosis.

Key words: Colon neoplasms, Tumor suppressor protein p53, Ubiquitinlike with PHD and ring finger domains 1