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Expression of Interferon Regulatory Factors in Breast Cancer Tissue

机译:干扰素调节因子在乳腺癌组织中的表达

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Purpose As neoplasia is the result of unbalanced cell growth and cell death, alternations in the growth control pathway including the immunity within the individual host-tumor relationship has been attributed to the development of breast cancer. Interferon(IFN)-γ based immunity was recently reported to have an antitumor effect and some new methods to assess the state of interferon-γ based immunity have been introduced. Interferon regulatory factor(IRF)-1 and interferon regulatory factor(IRF)-2 are transcriptional factors that mediate the effects of Interferon-γ. It was suggested that the loss of IRF-1 expression is associated with the loss of tumor suppression and the development of IRF-2 expression is associated with oncogenic activation. Thus, we studied the significances of the IRF-1 and IRF-2 expressions as they are related with some clinicopathological parameters to determine the biological behavior of breast cancer including the menopausal status, tumor size, lymph node status, histologic grade, the expression of steroid receptors, the expression of c-erb B2 oncoprotein and the expression of p53 protein. Methods Formalin-fixed paraffin embedded specimens from 82 patients with invasive ductal carcinoma were used to evaluate the expression of IRF-1 and IRF-2 by performing immunohistochemical staining with using an avidin-biotin-peroxidase complex technique. Results The expression of IRF-1 was observed in 80.5% of the study group. However, the expression of IRF-1 did not show any correlation with menopausal status, tumor size, histologic grade, the expression of steroid receptors, the expression of c-erb B2 oncoprotein and the p53 expression. Only lymph node metastasis showed a decreasing tendency of IRF-1 expression, but this was without statistical significance ( p =0.075). The expression of IRF-2 was observed in 58.5% of the study group and it did not show any significant relationship with any of the above mentioned clinicopathological parameters. Conclusion This study suggests that the expression of IRF-1 and IRF-2 does not affect the previously established parameters for determining such biological behaviors of breast cancer as the tumor size, lymph node metastasis, the histologic grade, the expression of steroid receptors, the expression of c-erb B2 and the expression of p53. In spite of these results, We'd like to recommend that another study be done to evaluate the role of IRF-1 and IRF-2 for the proper selection of the patients who are suitable for immunotherapy.
机译:目的由于瘤形成是细胞生长和细胞死亡失衡的结果,因此生长控制途径的改变(包括个体宿主-肿瘤关系中的免疫力)已归因于乳腺癌的发展。最近报道了基于干扰素(IFN)-γ的免疫具有抗肿瘤作用,并且已经引入了一些评估基于干扰素-γ的免疫状态的新方法。干扰素调节因子(IRF)-1和干扰素调节因子(IRF)-2是介导干扰素-γ作用的转录因子。提示IRF-1表达的丧失与肿瘤抑制的丧失有关,而IRF-2表达的发展与致癌激活有关。因此,我们研究了IRF-1和IRF-2表达与一些临床病理参数有关的意义,以确定乳腺癌的生物学行为,包括更年期,肿瘤大小,淋巴结状态,组织学分级,类固醇受体,c-erb B2癌蛋白的表达和p53蛋白的表达。方法对82例浸润性导管癌患者用福尔马林固定的石蜡包埋标本,采用抗生物素蛋白-生物素-过氧化物酶复合物进行免疫组织化学染色,评价IRF-1和IRF-2的表达。结果在研究组中有80.5%的IRF-1表达。但是,IRF-1的表达与绝经状态,肿瘤大小,组织学分级,类固醇受体的表达,c-erb B2癌蛋白的表达以及p53的表达均无相关性。仅淋巴结转移显示IRF-1表达下降趋势,但无统计学意义(p = 0.075)。在研究组中有58.5%的人观察到IRF-2的表达,并且与上述任何临床病理参数没有显着关系。结论这项研究表明,IRF-1和IRF-2的表达不会影响先前确定的确定乳腺癌生物学行为的参数,如肿瘤大小,淋巴结转移,组织学分级,类固醇受体的表达,肿瘤的表达等。 c-erb B2的表达和p53的表达。尽管取得了这些成果,我们想建议另一项研究中做以评估谁是适合于免疫治疗的患者选择适当的IRF-1和IRF-2的作用。

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