期刊文献+

细胞核增殖抗原、p53及表皮生长因子受体在结直肠癌组织的表达及其临床意义 被引量:7

The clinical significance of proliferation cell nuclear antigen, p53 and Epidermal Growth Factor Receptor expression in colorectal cancer
原文传递
导出
摘要 目的探讨结直肠癌组织中细胞核增殖抗原(Ki-67)、p53及表皮生长因子受体(EGFR)表达的临床意义.方法采用免疫组织化学法,观察Ki-67、p53、EGFR在120例结直肠癌组织的表达,应用x2检验、Fisher确切概率法、Spearman秩相关、生存分析等统计学方法,探讨其与临床病理特征及预后的关系.结果 120例结直肠癌Ki-67、p53及EGFR高表达率分别为63.3%、70.0%、3.3%.Ki-67、p53的表达呈正相关(r=0.300,P<0.05).Ki-67在年龄、国际抗癌联盟(UICC)分期上差异有统计学意义(x2=4.125、5.008,P<0.05);p53在淋巴结转移、组织学分级上差异有统计学意义(x2=7.372、10.088,P<0.05).单因素生存分析显示:Ki-67高表达与预后显著相关(x2=14.678,P<0.05).多因素生存分析显示:p53高表达[风险比(HR):0.276,95%可信区间(CI):0.100 ~0.762,P<0.05]和Ki-67高表达(HR:0.303,95% CI:0.121 ~0.758,P<0.05)是结直肠癌预后的独立危险因素,p53和Ki-67高表达组总生存期短于p53或Ki-67高表达组差异有统计学意义(HR:0.318,95% CI:0.148 ~0.683,P<0.05).结论 p53高表达和Ki-67高表达的组合定义了较小的患者组,其预后更差. Objective To investigate the clinical significance of expression of proliferation cell nuclear antigen (Ki-67), p53 and epidermal growth factor receptor (EGFR) in colorectal cancer. Methods Immunohistochemistry was used to detect Ki-67, p53 and EGFR protein expressions in 120 cases of colorectal cancer, the χ2 test, Fisher’s exact probabilities, Spearman’s rank correlation, survival analysis were used to explore the relationship between the expression and clinicopathological characteristics and prognosis. Results The high expression rates of Ki-67, p53 and EGFR in 120 cases of colorectal cancer were 63.3%, 70.0% and 3.3%, respectively. Expressions of Ki-67 and p53 were positively correlated (r=0.300, P<0.05). Ki-67 showed significant differences in age and UICC stage (χ2=4.125, 5.008, P<0.05). p53 showed significant differences in lymph node metastasis and histological grade (χ2=7.372, 10.088, P<0.05). Single-factor survival analysis showed that Ki-67 expression was significantly correlated with prognosis (χ2=14.678, P<0.05). Multi-factor survival analysis showed that high p53 expression [hazard ratio (HR): 0.276, 95% confidence interval (CI): 0.100-0.762, P<0.05], and high expression of Ki-67 (HR: 0.303, 95%CI: 0.121-0.758, P<0.05) are independent risk factors for colorectal cancer prognosis, the overall survival time of the group with high expression of p53 and ki-67 was shorter than that of the group with high expression of p53 or Ki-67, which was statistically significant (HR: 0.318, 95%CI: 0.148-0.683, P<0.05). Conclusion The combination of high expression of p53 and high expression of Ki-67 defines a smaller group of patients with worse prognosis.
作者 查汉益 张海山 智一晓 刘希凡 范嵩 张文涛 沈可欣 Zha Hanyi;Zhang Haishan;Zhi Yixiao;Liu Xifan;Fan Song;Zhang Wentao;Shen Kexin(Department of Gastrointestinal Colorectal and Anal Surgery,China-Japan Union Hospital of Jilin University,Changchun 130033,China;Department of Hepatobiliary and Pancreatic Medicine,the First Hospital of Jilin University,Changchun 130021,China)
出处 《中华实验外科杂志》 CAS CSCD 北大核心 2019年第10期1850-1853,共4页 Chinese Journal of Experimental Surgery
关键词 细胞核增殖抗原 P53 表皮生长因子受体 预后 结直肠癌 Proliferation cell nuclear antigen p53 Epidermal growth factor receptor Prognosis Colorectal cancer
  • 相关文献

参考文献6

二级参考文献45

  • 1Derya Gumurdulu,Seyda Erdogan,Fazilet Kayaselcuk,Gulsah Seydaoglu,Cem K Parsak,Orhan Demircan,Ilhan Tuncer.Expression of COX-2, PCNA, Ki-67 and p53 in gastrointestinal stromal tumors and its relationship with histopathological parameters[J].World Journal of Gastroenterology,2007,13(3):426-431. 被引量:21
  • 2Ferlay J, Soerjomataram I, Ervik M,et al. GLOBOCAN 2012vl.O,Cancer Incidence and Mortality Worldwide : I ARC CancerBase No. 11 [M/OL]. Lyon, France: International Agencyfor Research on Cancer. [2014-01-20]. http: //globocan. iarc. fr.
  • 3Di Carlo A,Mariano A, Terracciano D, et al. Matrixmetalloproteinase-2 and -9 in the urine of prostate cancerpatients[J]. Oncol Rep, 2010,24( 1) : 3-8.
  • 4Yin Y, Zeng K,Wu M, et al. The levels of Ki-67 positive arepositively associated with lymph node metastasis in invasiveductal breast cancer[J]. Cell Biochem Biophys, 2014,70(2):1145-1151.
  • 5Albini A, Sporn MB. The tumour microenvironment as atarget for chemoprevention[jj. Nat Rev Cancer, 2007,7 (2):139-147.
  • 6Colvin EK. Tumor-associated macrophages contribute to tumorprogression in ovarian cancer[J/OL]. Front Oncol, 2014,4 :137[2014-06-06]. http: //journal, frontiersin. org/article/10.3389/fonc. 2014. 00137/full.
  • 7Loffek S,Schilling O,Franzke CW. Series " matrixmetalloproteinases in lung health and disease": biological roleof matrix metalloproteinases: a critical balance[J]. Eur RespirJ, 2011,38(1):191-208.
  • 8Tabata K, Tanaka T, Hayashi T,et al. Ki-67 is a strongprognostic marker of non-small cell lung cancer when tissueheterogeneity is considered[J/OL]. BMC Clin Pathol* 2014,14:23[2014-05-13], http: // www. biomedcentral. com/1472-6890/14/23.
  • 9Hongjie Zhang,Xiaoyi Kuai,Zeyu Ji,Zhengyang Li,Ruihua Shi.Over-Expression of Small Ubiquitin-Related Modifier-1 and Sumoylated p53 in Colon Cancer[J]. Cell Biochemistry and Biophysics . 2013 (3)
  • 10Tae-Hyoung Yoo,Jin-Hee Lee,Hyang-Sook Chun,Sung-Gil Chi.α-Lipoic acid prevents p53 degradation in colon cancer cells by blocking NF-κB induction of RPS6KA4[J]. Anti-Cancer Drugs . 2013 (6)

共引文献64

同被引文献76

引证文献7

二级引证文献16

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