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首页> 外文期刊>Oncology letters >Correlation of CCL20 expression in rectal mucosa with the development of ulcerative colitis-associated neoplasia
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Correlation of CCL20 expression in rectal mucosa with the development of ulcerative colitis-associated neoplasia

机译:直肠粘膜中CCL20表达与溃疡性结肠炎相关瘤形成的关系

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Chronic inflammation increases the risk of developing several gastrointestinal malignancies. Chemokines that are produced by colonic epithelial cells play significant roles in the maintenance and repair of the epithelial barrier. The present study aimed to clarify whether the expression of CCL20 and its receptor, CCR6, was correlated with the development of ulcerative colitis (UC)-associated neoplasia. A total of 93 patients with UC who underwent proctocolectomies were enrolled in the present study. Immunohistochemical analysis for CCL20 and CCR6 expression in the rectal mucosa was performed and the correlation between expression and the pathogenesis of UC-associated neoplasia was investigated. A total of 16 (17.2%) patients presented with UC-associated neoplasia. The immunohistochemistry (IHC) score for CCL20 was significantly increased in the patients with a mild form of the disease (P=0.0363). The IHC score for CCL20 expression in the patients with UC-associated neoplasia was higher compared with the patients without neoplasia (P=0.0294). In contrast, there was no significant correlation between CCR6 expression and the clinicopathological variables. The logistic regression analysis revealed that a high IHC score for CCL20 expression in the rectal mucosa and a disease duration of more than eight years were significantly correlated with the development of UC-associated neoplasia (P<0.05). The results suggest that an evaluation of CCL20 expression in the rectal mucosa may be useful to identify patients who are at a high risk for developing UC-associated neoplasia. However, a selection bias existed in the present study due to the fact that the patient population that was enrolled was not representative of a typical surveillance patient population.
机译:慢性炎症增加了发生几种胃肠道恶性肿瘤的风险。结肠上皮细胞产生的趋化因子在上皮屏障的维持和修复中起重要作用。本研究旨在阐明CCL20及其受体CCR6的表达是否与溃疡性结肠炎(UC)相关的肿瘤形成有关。本研究共纳入了93例接受了结肠直肠切除术的UC患者。进行了直肠黏膜中CCL20和CCR6表达的免疫组织化学分析,并研究了其与UC相关肿瘤的发病机制之间的相关性。共有16名(17.2%)患者出现了UC相关性肿瘤。轻度疾病患者的CCL20免疫组织化学(IHC)评分显着提高(P = 0.0363)。 UC相关性肿瘤患者的CCL20表达的IHC评分高于无肿瘤的患者(P = 0.0294)。相反,CCR6表达与临床病理变量之间无显着相关性。 Logistic回归分析显示,直肠粘膜中CCL20表达的IHC评分较高以及疾病持续时间超过8年与UC相关性瘤形成的发生密切相关(P <0.05)。结果表明,对直肠粘膜中CCL20表达的评估可能有助于确定罹患UC相关肿瘤的高风险患者。但是,由于所招募的患者人群并不代表典型的监测患者人群,因此本研究存在选择偏见。

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