CDX2和Ki-67在胃癌中的表达及其与临床病理参数的关系

Chatpalli Pranjali, Kamath Sulatha, Mysorekar Vijaya V
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引用次数: 0

摘要

背景:CDX2已被确定为结直肠癌的良好预后标志物。分化腺癌的特点是CDX2表达高于未分化肿瘤,在肠道表型上具有更强的反应性。肿瘤分化程度与Ki-67评分密切相关。CDX2强表达与低Ki-67指数相关,而CDX2阴性或弱表达与高Ki-67指数相关。方法:对胃癌活检和胃切除术标本进行临床病理检查,免疫组化(IHC)染色检测CDX2和Ki-67的表达。评估两种标志物与各临床病理参数的关系。对数据进行统计学分析。P<0.05为差异有统计学意义。结果:57例胃腺癌患者,平均年龄56.12岁。除肿瘤位置和浸润深度外,CDX2和Ki-67与临床、肉眼及显微镜参数均无显著相关性。CDX2 (p=0.04)、Ki-67 (p=0.03)与肿瘤位置有显著相关性。肿瘤浸润深度与Ki-67有显著相关性(p=0.013)。CDX2与Ki-67之间无显著相关性。结论:CDX2和Ki-67与临床病理参数的统计相关性证明CDX2和Ki-67是肿瘤部位和浸润深度(Ki-67)的独立标志物。但由于缺乏CDX2与Ki-67的相关性,进一步的研究需要更大的样本量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CDX2 and Ki-67 Expression in Gastric Carcinoma and Its Association with Clinocopathological Parameters
Background: CDX2 has been established as a good prognostic marker for colorectal carcinomas. Differentiated adenocarcinomas are characterized by higher CDX2 expression than undifferentiated tumors with stronger reactivity in intestinal phenotypes. There is a close correlation between the degree of tumor differentiation and the Ki-67 score. It was also observed that strong CDX2 expression was associated with low Ki-67 index whereas negative or dim CDX2 expression was associated with high Ki-67 index. Methods: Gastric biopsies and gastrectomy specimens with gastric carcinoma were evaluated clinicopathologically and processed for immunohistochemistry (IHC) staining to assess CDX2 and Ki-67 expression. The relationship between 2 markers and each clinicopathological parameter was evaluated. Data was statistically analysed. P<0.05 were taken for statistical significance. Results: The study was done on 57 gastric adenocarcinoma cases with mean age 56.12 years. No significant correlation was found between CDX2 & Ki-67 with clinical, gross & microscopic parameters except for tumor location and depth of invasion. Significant correlation was detected between CDX2 (p=0.04) & Ki-67 (p=0.03) with tumor location. Depth of tumor invasion was significantly associated with Ki-67 (p=0.013). No significant association between CDX2 and Ki-67 was observed. Conclusion: The statistical correlation between CDX2 & Ki-67 with clinicopathological parameters proves that CDX2 & Ki-67 to be the independent markers with respect to tumor site and depth of invasion (in case of Ki-67). But due to lack of association of CDX2 with Ki-67 further studies need to be done with higher sample size.
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