临床肿瘤学杂志

• 论著 • 上一篇    下一篇

ANXA4和ANXA6在肝门部胆管癌中的表达及临床意义

李超富1,俞文隆2,于观贞3,高勇4   

  1. 1 200120 上海 大连医科大学东方医院肿瘤科 2 200438 东方肝胆外科医院外科 3 200032 上海中医药大学附属龙华医院肿瘤科 4 200120 同济大学附属东方医院肿瘤科
  • 收稿日期:2017-04-27 修回日期:2017-07-03 出版日期:2017-08-31 发布日期:2017-08-31
  • 通讯作者: 高勇

Expressions of ANXA4 and ANXA6 in hilarcholangiocarcinoma and their clinical significance

LI Chaofu,YU Wenlong,YU Guanzhen,GAO Yong   

  1. Department of Oncology,East Hospital,Dalian Medical University,Shanghai 200120,China
  • Received:2017-04-27 Revised:2017-07-03 Online:2017-08-31 Published:2017-08-31
  • Contact: GAO Yong

摘要: 目的 探讨膜联蛋白A4(ANXA4)和膜联蛋白A6(ANXA6)在肝门部胆管癌(HC)组织中的表达及两者与HC临床病理特征和预后的关系。方法 采用组织芯片与免疫组织化学技术检测2005年至2007年49例HC组织及10例癌旁组织中ANXA4和ANXA6的表达情况,分析两者表达与HC临床病理特征及预后的关系。结果 ANXA4和ANXA6在HC组织中的阳性表达率分别为63.3%(31/49)和69.4%(34/49),明显高于癌旁组织的20.0%(2/10)和30.0%(3/10),差异均有统计学意义(P<0.05)。ANXA4蛋白表达与淋巴结转移有关(P<0.05),ANXA6表达则与肿瘤大小、淋巴结转移及TNM分期有关(P<005)。ANXA4阳性表达者的中位总生存时间(OS)和无进展生存时间(PFS)分别为14个月和12个月,明显短于阴性表达者的46个月和39个月(P<0.05);ANXA6阳性表达者的中位OS和PFS分别为14个月和12个月,明显短于阴性表达者的42个月和39个月(P<0.05)。Cox多因素分析显示,ANXA6、浸润深度是影响OS的独立因素,浸润深度是影响PFS的独立因素。结论 ANXA4和ANXA6与HC的发生、发展有关,且ANXA6是潜在的评估预后的肿瘤标志物。

Abstract: Objective To explore the expressions of Annexin A4(ANXA4)and Annexin A6(ANXA6)protein in hilarcholangiocarcinoma(HC)and to determine their relationships with clinical parameters and prognosis. Methods The expressions of ANXA4 and ANXA6 were detected by tissue microarray and immunohistochemistry in 49 HC tissues and 10 tumor adjacent tissues from 2005 to 2007.The relationships between the expressions of ANXA4 and ANXA6 and clinical parameters were analyzed,as well as prognosis. Results The positive rates of ANXA4 and ANXA6 in HC tissues(63.3%,69.4%)were significantly higher than those(20.0%,30.0%)in tumor adjacent tissues(P<0.05). The expression of ANXA4 was closely associated with lymph node metastasis(P<0.05). The expression of ANXA6 was closely associated with tumor size,lymph node metastasis and TNM stage(P<0.05). The median overall survival(OS)and progression-free survival(PFS)of patients with ANXA4 positive expression was 14 months and 12 months,shorter than 46 months and 39 months of patients with ANXA4 negative expression(P<0. 05). The median OS and PFS of patients with ANXA6 positive expression was 14 months and 12 months,shorter than 42 months and 39 months of patients with ANXA6 negative expression(P<0.05). Multivariate analysis revealed that ANXA6 and invasion depth were independent prognostic factors influencing OS,and invasion depth was also an independent factor influencing PFS. Conclusion ANXA4 and ANXA6 are associated with occurrence and development of HC,and ANXA6 may be a new tumor marker for predicting prognosis of HC.

No related articles found!
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!