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Possible prognostic significance of p53 cyclin D1 and Ki-67 in the second primary malignancy of patients with double primary malignancies

机译:p53cyclin D1和Ki-67在双原发恶性肿瘤患者第二原发恶性肿瘤中可能的预后意义

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摘要

Patients with two types of primary cancers are rare. In this study, we investigated the expression of p53, cyclin D1, and Ki-67 in the second primary malignancy. Tissue samples were obtained from the second primary cancer site of 43 patients who met the diagnostic criteria for double primary cancer. p53, cyclin D1 and Ki-67 were determined using immunohistochemistry. Categorical variables were compared using the Chi-squared test; correlation between data scores and histology was calculated using the Spearman’s rank-order correlation. The expression rates of p53, cyclin D1 and Ki-67 in the second primary malignancy site were 60.5%, 30.2% and 65.1% respectively. p53 expression showed statistically significant association with tumor occurrence interval, pathological grading and nodal metastasis (p < 0.05). Positive correlation was detected between the expression of cyclin D1 and Ki-67 and the expression of p53 (r = 0.313, p = 0.041; r = 0.319, p = 0.037, respectively). High-expressing p53 or cyclin D second primary malignancies were associated with decreased overall survival (p = 0.040 and p = 0.043, respectively). Ki-67 expression levels did not exhibit statistically significant differences in survival. In conclusion, elevated protein expression of p53, cyclin D1 and Ki-67 in the second primary malignancy is an indicator of more aggressive malignant behavior of the secondary tumor. These markers may have prognostic value in the clinical setting.
机译:患有两种原发性癌症的患者很少。在这项研究中,我们调查了p53,cyclin D1和Ki-67在第二原发恶性肿瘤中的表达。从43名符合双重原发癌诊断标准的患者的第二原发癌部位获得组织样品。使用免疫组织化学测定p53,细胞周期蛋白D1和Ki-67。使用卡方检验比较分类变量。数据得分和组织学之间的相关性是使用Spearman的排名相关性来计算的。 p53,cyclin D1和Ki-67在第二原发恶性肿瘤部位的表达率分别为60.5%,30.2%和65.1%。 p53表达与肿瘤发生间隔,病理分级和淋巴结转移有统计学意义(p <0.05)。检测到细胞周期蛋白D1和Ki-67的表达与p53的表达呈正相关(r = 0.313,p = 0.041; r ​​= 0.319,p = 0.037)。高表达的p53或cyclin D第二原发性恶性肿瘤与总体生存期降低相关(分别为p = 0.040和p = 0.043)。 Ki-67表达水平在生存率上无统计学差异。总之,在第二原发性恶性肿瘤中p53,细胞周期蛋白D1和Ki-67的蛋白表达升高是继发性肿瘤更具侵略性的恶性行为的指示。这些标志物可能在临床上具有预后价值。

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