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转录因子FOXP1在胃癌组织中的表达及意义
引用本文:刘剑尚鑫沙素梅夏丽敏吴开春.转录因子FOXP1在胃癌组织中的表达及意义[J].现代生物医学进展,2014,14(5):814-818.
作者姓名:刘剑尚鑫沙素梅夏丽敏吴开春
作者单位:第四军医大学西京消化病医院肿瘤生物学国家重点实验室,陕西西安710032
基金项目:国家重点基础研究发展计划“973项目”(2010cB529302);国家自然科学基金项目(81272652;81172290;91129723)
摘    要:目的:检测FOXP1蛋白在胃癌组织及癌旁正常组织中的表达情况,并探讨其与胃癌患者病理参数及预后的关系。方法:采用免疫组织化学染色方法检测90例胃癌组织和相应癌旁正常组织中FOXP1的表达情况并进行评分,进一步统计分析FOXP1表达与胃癌患者临床病理参数以及预后的关系。结果:FOXP1在胃癌组织中的表达显著低于癌旁正常组织(P0.01);对临床资料进行统计分析表明,在临床III期和IV期患者的胃癌组织中FOXP1的表达显著低于临床I期和II期的患者(P0.05);FOXP1在低分化胃癌中的表达显著低于高、中分化胃癌(P0.01);FOXP1表达阳性者术后总体生存率较表达阴性者高(P=0.145),中位生存期长。结论:FOXP1表达的减少可能参与了胃癌的发生发展,FOXP1在胃癌中可能扮演抑癌基因的角色,FOXP1可作为胃癌治疗的潜在靶点。

关 键 词:FOXP1蛋白  胃癌  免疫组织化学  抑癌基因

Expression and Significance of Forkhead Box P1 in the Tissues of Gastric Cancer*
LIU Jian,SHANG Xin,SHA Su-mei,XIA Li-min. WU Kai-chun.Expression and Significance of Forkhead Box P1 in the Tissues of Gastric Cancer*[J].Progress in Modern Biomedicine,2014,14(5):814-818.
Authors:LIU Jian  SHANG Xin  SHA Su-mei  XIA Li-min WU Kai-chun
Institution:LIU Jian, SHANG Xin, SHA Su-mei, XIA Li-min, WU Kai-chun (State Key Laboratory of Cancer Biology and Xijing Hospital of Digestive Disease, The Fourth Military Medical Universi(y, Xi'an, Shaanxi, 710032, China)
Abstract:Objective: To investigate the expression and clinical significance of Forkhead box PI(FOXP1) protein in gastric cancer tissues and adjacent non-tumor tissues. Methods: Immunohistochemistry was used to detect the expression of FOXP1 in 90 gastric cancer tissues and paired adjacent non-tumor tissues. Statistic analyses were explored to value its correlation with the clinicopathological characteristics and prognosis. Results: FOXP1 expression was significantly decreased in gastric cancer tissues compared with the corresponding adjacent non-tumor tissues (P〈0.01). Further analysis about its correlation with the clinicopathological characteristics showed that FOXP1 expression was significantly lower in patients of clinical HI-IV stage than in I-II stage (P〈0.05). The expression of FOXP1 was significantly lower in poorly differentiated gastric cancer than in moderately and well differentiated gastric cancer (P〈0.01). Patients with FOXP1 positive expression had a better prognosis and longer median survival time than those with negative expression (P=0.145). Conclusions: The decreased FOXP 1 expression may contribute to gastric cancer initiation and progression. FOXP 1 may play its role as a tumor suppressor in gastric cancer. FOXP1 is a potential therapeutic target in gastric cancer.
Keywords:Forkhead box P 1 (FOXP 1)  Gastric cancer  Immunohistochemistry  Tumor suppressor gene
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