实用器官移植电子杂志 ›› 2013, Vol. 1 ›› Issue (2): 107-111.

• 论著 • 上一篇    下一篇

肝细胞肝癌中生长抑素受体 2/5 的表达研究

李姗霓,孙丽莹
  

  1. 天津市第一中心医院器官移植中心移植内科,天津 300192
  • 出版日期:2013-03-20 发布日期:2021-04-20
  • 基金资助:
    国家高技术研究发展计划(863)项目(2012AA021001)

Characterization of somatostatin receptor 2/5 expression in operable hepatocellular carcinomas

LI Shan-ni,SUN Li-ying.
  

  1. Department of Liver Transplant,First Center Hospital,Tianjin 300192,China
  • Online:2013-03-20 Published:2021-04-20

摘要:

目的 观察生长抑素受体(SSTR)-2/5 在人原发性肝细胞肝癌及癌旁组织的表达,探讨其临床意义。方法 选择 2008 年 2 月至 2010 年 7 月期间在天津市第一中心医院住院手术治疗的 22 例肝细胞肝癌患者,切取病理组织,采用免疫组化和实时荧光定量聚合酶链反应(PCR)方法检测 SSTR-2/5 在肝癌及癌旁组织中的表达,并比较其与临床病理参数的关系。结果 癌旁组织和肝癌组织中 SSTR-2/5 均呈阳性表达 ;肝癌组织 SSTR-2/5 表达明显低于癌旁肝硬化组织〔SSTR-2 mRNA(RQ 值):1.89±0.74 比2.54±0.80,SSTR-5 mRNA(RQ 值):3.61±1.66 比 6.78±4.27;SSTR-2蛋白:68.2%(12/22)比 95.5%(21/22),SSTR-2/5 蛋白均为 95.5%(21/22);均 P<0.05〕。全部患者术后平均无瘤生存期为 27.3 个月,SSTR-2/5 高表达组较低表达组无瘤生存期延长(log-rank=4.08,P=0.043)。结论 SSTR 低表达预后相对较差,SSTR表达的表征可以被用来作为评估肝癌预后的有用参数。

关键词:

Abstract:

Objects To analyze the expression of somatostatin receptor(SSTR)-2/5 in HBV-relatedhepatocellular carcinomas(HCC)and compare its clinicopathological features and follow-up data. Methods 22patients diagnosed with HCC between February 2008 and July 2010 underwent radical liver resection. Expression ofSSTR-2/5 in HCC and adjacent cirrhotic tissues were examined by immunohistochemistry and real time polymerasechain reaction(PCR). Moreover,the relationship between SSTR expression and clinicopathological features werealso compared. The patients had routine follow-up exams until cancer reoccurred. Results Adjacent cirrhoticliver and HCC expressed SSTR-2/5. Compared to adjacent cirrhotic liver tissues,expression of SSTR-2/5 in tumorswere significantly lower〔SSTR-2 mRNA(RQ):1.89±0.74 vs. 2.54±0.80,SSTR-5 mRNA(RQ):3.61±1.66vs. 6.78±4.27 ;SSTR-2 protein :68.2%(12/22)vs. 95.5%(21/22),SSTR-2/5 protein :both 95.5%(21/22),all P<0.05〕. The mean progression free survival for all patients was 27.3 months. The high SSTR-2/5 expressiongroup had significantly improved the progression free survival compared to the low expression group(log-rank=4.08,P=0.043). Conclusions Down regulation of SSTR transcription may result in loss of a tumor suppressive.Characterization of SSTR expression can be used as a useful parameter to evaluate the prognosis of HCC.

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