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应用组织芯片技术研究人类肺癌中EphB4、HIF-1α和IGF-Ⅱ表达的生物学意义 被引量:1

A study on biological significance of expression of EphB4,HIF-1α and IGF-Ⅱ in lung cancer through tissue microarray technique
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摘要 目的应用组织芯片技术探讨人类肺癌中EphB4、HIF-1α和IGF-Ⅱ的表达情况以及三者表达的生物学意义。方法构建一个包含54例肺癌和10例正常肺组织的组织芯片蜡块,应用免疫组化SP法检测其EphB4、HIF-1α和IGF-Ⅱ蛋白的表达情况。结果病例组中EphB4、HIF-1α和IGF-Ⅱ蛋白的阳性率分别是44.4%、46.3%和42.6%,显著高于正常对照组(P<0.05);这三种蛋白的表达与肿瘤的大体类型、分化程度和TNM分期密切相关(P<0.05),而与患者性别、年龄、有无淋巴结转移无关(P>0.05)。三种蛋白的表达彼此之间存在显著正相关关系(P<0.01)。结论EphB4、HIF-1α和IGF-Ⅱ蛋白的表达可能与肿瘤的发生和恶性行为有关,三者之间存在着相互作用。 Objective To investigate the relationship among the expression of EphB4. HIF-laand IGF-Ⅱ in lung cancer and its biological significances. Methods Constructing a block with 54 lung cancer and 10 normal lung tissue on it. The expression of EphB4 .HIF-1α and IGF Ⅱwere detected in these specimens by using streptavidin-peroxidase (SP) immunohistochemical method, and 10 normal lung tissues as control. Results Among the 54 cases of lung cancer.the positive rate of EphB4 was 44.4 % 46. 3% of the tumors were positive for HIF-1α and 42. 6 %were positive for IGF-Ⅱ These three kinds of proteins expression were related to gross types,differentiations and clinical stages ( P〈0.05 ). but not to histological classification, age.sex and lymphoid metastasis( P〉0.05 ). A highly positive correlation was observed between EphB4, HIF-1α and IGF- Ⅱ each other( P〈0.01 ). Conclusions Overexpression of EphB4, HIF-1α and IGF- Ⅱ may play an important role in the pathogenesis, progression and malignant degree of lung cancer. There are interaction between them each other.
出处 《国际呼吸杂志》 2006年第10期721-723,F0003,共4页 International Journal of Respiration
基金 天津市科委重点攻关课题资助项目(033804211)
关键词 组织芯片 肺癌 EPHB4 HIF—1α IGF-Ⅱ 免疫组织化学 Tissue microarray Lung cancer EphB4 HIF- 1 α IGF- Ⅱ , Immunohistochemical
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同被引文献4

  • 1郝静,王秀问,蔡毅然,孙殿水,李蓓.急、慢性乏氧标记物(HIF-1α、GLUT1)表达在晚期非小细胞肺癌患者中的临床意义[J].中国肿瘤临床,2006,33(5):294-295. 被引量:3
  • 2Yasuda H, Nakayama K, Watanabe M, et al. Nitroglycerin treatment may enhance chemosensitivity to docetaxel and carboplatin in patients with lung adenocarcinoma. Clin Cancer Res, 2006, 12 (22) :6748 -6757.
  • 3Chang C C, Lin M T, Lin B R, et al. Effect of connective tissue growth factor on hypoxia-inducible factor lalpha degradation and tumor angiogenesis. J Natl Cancer Inst, 2006,19,98 ( 14 ) : 984 - 995.
  • 4Swinson D E, O'Byrne K J. Interactions between hypoxia and epidermal growth factor receptor in non-small-cell lung cancer. Clin Lung Cancer,2006,7 (4) :250 - 256.

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