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CIP2A overexpression is associated with c-Myc expression in colorectal cancer

机译:CIP2A过表达与大肠癌中c-Myc表达相关

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Background: To improve the prognostic evaluation of colorectal cancer requires new molecular markers. Cancerous inhibitor of protein phosphatase 2A (CIP2A) serves as an oncoprotein by targeting PP 2A-mediated inhibition of c-Myc. A prognostic role for CIP2A has been demonstrated in gastric, lung and tongue cancers. Results: CIP2A was overexpressed in 661 (87.9%) specimens. CIP2A overexpression was associated with tumor differentiation grade (p = 0.014), p53 immunopositivity (p = 0.042), EGFR immunopositivity (p = 0.007) and c-Myc nuclear immunopositivity (p = 0.018). In survival analysis, CIP2A failed to show any prognostic significance (p = 0.270, log-rank test). Methods: 863 consecutive colorectal cancer patients treated at Helsinki University Central Hospital in 1983-2001 were collected with 752 scored successfully for CIP2A immunohistochemical expression from tumor tissue microarrays. Associations with clinicopathologic variables and molecular markers were explored by the chi-square test, and the Kaplan-Meier method served for survival analysis. Conclusions: Overexpression of CIP2A in colorectal cancer patients may be an important step in colorectal carcinogenesis. Based on our findings, CIP2A shows no association with patient prognosis in colorectal cancer, but is associated with nuclear c-Myc.
机译:背景:为了改善大肠癌的预后评估,需要新的分子标记。蛋白磷酸酶2A的癌性抑制剂(CIP2A)通过靶向PP 2A介导的c-Myc抑制作用而作为癌蛋白。已经证明CIP2A在胃癌,肺癌和舌癌中具有预后作用。结果:CIP2A在661个样本中过表达(占87.9%)。 CIP2A过表达与肿瘤分化程度(p = 0.014),p53免疫阳性(p = 0.042),EGFR免疫阳性(p = 0.007)和c-Myc核免疫阳性(p = 0.018)相关。在生存分析中,CIP2A未能显示任何预后意义(p = 0.270,对数秩检验)。方法:收集1983-2001年在赫尔辛基大学中心医院接受治疗的863例大肠癌患者,并从肿瘤组织微阵列中成功获得752例CIP2A免疫组化表达的评分。卡方检验探讨了与临床病理变量和分子标志物的关联,Kaplan-Meier方法用于生存分析。结论:CIP2A在大肠癌患者中的过度表达可能是大肠癌发生的重要步骤。根据我们的发现,CIP2A与结直肠癌的患者预后无关,但与核c-Myc相关。

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