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胃癌表达Her-2的情况和临床分期的联系 被引量:2

Expression of Her-2 in Stomach Cancer and Its Relationship with Clinical Staging
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摘要 目的:探讨人表皮生长因子受体2(Her-2)在胃癌中的表达情况以其与胃癌临床分期的联系。方法:选取笔者所在医院就诊的237例胃癌病例,利用免疫组织化学染色法分别检测每个患者手术标本中肿瘤组织与正常胃黏膜的Her-2蛋白的表达情况,进行比较。结果:肿瘤组织Her-2表达的阳性率为26.58%,显著高于正常胃黏膜Her-2表达的阳性率为0%,两组比较差异有统计学意义(P<0.05)。此外,Her-2在胃癌组织中的可疑阳性率31.65%亦显著高于正常胃组织5.06%,两组比较差异有统计学意义(P<0.05)。Ⅳ期患者胃癌标本Her-2蛋白表达的阳性率达64.28%,显著高于Ⅲ、Ⅱ、Ⅰ期,比较差异均有统计学意义(P<0.05);并且随着胃癌分期水平的减低,Her-2阳性率亦随之降低,两者呈正相关。结论:与正常胃黏膜相比,Her-2蛋白在胃癌组织中的表达率显著增高,并且与胃癌分期呈现正相关。 Objective:To explore the expression of Her-2 in stomach cancer and its relation with clinical staging.Method:273 cases of lung cancer in our hospital were selected,then detected the expression of Her-2 in tumour tissues and normal tissues by immunohistochemistry stain and compared the results.Result:The positive rate of Her-2 protein in tumour tissues was 26.58%,which was significantly higher than that in gastric mucosa 0%,the difference was statistically significant(P〈0.05).Besides,the suspected positive rate of Her-2 in tumour tissues was significantly higher than that in gastric mucosa(P〈0.05). The statistics showed that the positive Her-2 expression in IV stage was 64.29%,which was significantly higher than stageⅢ,Ⅱ,Ⅰ,and the differences were statistically significant(P〈0.05),with the reduce of staging level for lung cancer,the positive of Her-2 had reduced,which showed positive correlation between them.Conclusion:The expression level of Her-2 in lung cancer tissues is significantly higher than normal gastric mucosa,and it has positive correlation with cancer staging.
作者 凌航 俞训彬
机构地区 福建省立医院
出处 《中外医学研究》 2014年第26期53-54,共2页 CHINESE AND FOREIGN MEDICAL RESEARCH
关键词 胃癌 人类表皮生长因子受体2 免疫组化 临床分期 Lung cancer Human epidermal growth factor receptor-2 Immunohistochemical Clinical staging
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  • 1冯秀丽.基于局限型与浸润型胃癌临床不同病理的特点及预后思路探索32例[J].医学信息(医学与计算机应用),2014,0(8):200-200. 被引量:1
  • 2Rosenfeld N, Aharonov R, Meiri E, et al.MicroRNAs accurately identify cancertissueorigin[J].NatBiotechnol, 2008, 26(4):462-469.
  • 3Ma Y' Y, Tao H Q. Microribonucleic acids and gastric cancer[J]. Cancer Sci, 2012, 103(4): 620-625.
  • 4Ueda T, Volinia S, Okumura H, et al.Relation between microRNA expression and progression and prognosis of gastric cancer: a microRNA expression analysis[J].Lancet Oncol, 2010, 11(2) : 136-146.
  • 5Mees S T, Mardin W A, Sielker S, et al.Involvement CD40 targeting microRNA-224 and miR-486 on the progression of pancreatic ductaladenocarcinomas[J].Ann Surg Oncol, 2009, 16(8): 2339-2350.
  • 6Gokhale A, Kunder R, Goel A, et al.Distinctive microRNA signature of medulloblastomas associated with the WNT signaling pathway[J]iCancer ResTher, 2010, 6(4): 521-529.
  • 7White N M, Chow T F, Mejia-Guerrero S, et al.Three dysregulated miRNAs control kallikrein 10 expression and cell proliferation in ovarian cancer[J].BrJCancer, 2010, 102(8): 1244-1253.
  • 8Li Q, Wang G, Shan J L, et al.MicroRNA-22g is upregulated in HepG2 cells and involved in cellular migration and invasion[J].Joumal of Gastroenterology and Hepatology, 2010, 25(1): 164-171.
  • 9詹文华,韩方海.我国胃癌外科治疗的现状和思考[J].实用肿瘤杂志,2008,23(2):91-93. 被引量:37
  • 10张维,高云升.S100A8在胃癌中的表达及临床意义[J].中国医学创新,2012,9(3):17-18. 被引量:3

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