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p27kip1 Expression Is Inversely Related to the Grade of Gastric MALT Lymphoma.

机译:p27kip1表达与胃MALT淋巴瘤的级别成反比。

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Background: Decreased or lost expression of the cyclin-dependent kinase inhibitor p27kip1 protein has been found to be a poor prognostic factor in many cancers, including gastric cancer. Aim: To evaluate p27kip1 expression in gastric mucosa–associated lymphoid tissue (MALT) and gastric B-cell lymphoma. Methods: Fifty-two cases of gastric lymphoma, mean age 68.7 yr (range 23–90 yr), 11 of chronic Helicobacter pylori–associated gastritis, and 5 of normal gastric mucosa were studied. Patients were classified into two groups. Stage IE gastric lymphomas were defined as local gastric lymphoma of MALT and more advanced stages as advanced gastric lymphoma. Twenty-three patients diagnosed as stage IE, 13 of these were low-grade and 10 diffuse large B-cell lymphoma (DLBL). Twenty-nine patients were at stage IIE or above, 18 with low-grade and 11 with DLBL. Serial sections were evaluated by immunohistochemistry after staining with antibodies against p27/Kip1 and Ki-67. Results: The proliferativeindex was higher in gastric DLBL than in low-grade MALT lymphomas, 57.1 ± 31.2 vs 17.3 ± 20.6 (p = 0.0001). The mean p27kip1 expression score for high-grade patients was significantly lower compared with that of low-grade patients, 0.5 ± 0.4 and 1.6±0.8, respectively (p = 0.001). Comparative evaluation of p27kip1 expression in malignant lymphoid cells revealed that B cells of the localized gastric DLBL patients expressed the least p27kip1, 0.36 ± 0.32. This value was lower than that of malignant lymphoid cells of patients with advanced DLBL, 0.64 ± 0.53, advanced low-grade MALT lymphoma, 1.59 ± 0.79, and localized low-grade MALT lymphoma, 1.59 ± 0.84. In the multivariate model in which all p27kip1 variables were entered, the expression of p27kip1 in malignant lymphoid cells was inversely correlated with the grade of the lymphoma irrespective of the stage of the disease (p = 0.0001), and significantly predicted grade: OR:0.07, 95% CI 0.07–0.31, p = 0.0001.Conclusion: p27kip1 may be a putative distinct molecular marker to differentiate between low-grade and high-grade gastric lymphoma.
机译:背景:已经发现,细胞周期蛋白依赖性激酶抑制剂p27kip1蛋白表达降低或丢失在许多癌症(包括胃癌)中都是不良的预后因素。目的:评估p27kip1在胃黏膜相关淋巴样组织(MALT)和胃B细胞淋巴瘤中的表达。方法:研究了52例胃淋巴瘤,平均年龄68.7岁(范围23-90岁),11例慢性幽门螺杆菌相关性胃炎和5例正常胃黏膜。患者分为两组。 IE期胃淋巴瘤定义为MALT的局部胃淋巴瘤,晚期则定义为晚期胃淋巴瘤。 23例被确诊为IE期的患者,其中13例为低度恶性,10例为弥漫性大B细胞淋巴瘤(DLBL)。 IIE或更高阶段的患者为29例,低度分级为18例,DLBL为11例。在用针对p27 / Kip1和Ki-67的抗体染色后,通过免疫组织化学评估连续切片。结果:胃DLBL的增殖指数高于低度MALT淋巴瘤,分别为57.1±31.2和17.3±20.6(p = 0.0001)。高等级患者的平均p27kip1表达得分显着低于低等级患者,分别为0.5±0.4和1.6±0.8(p = 0.001)。对恶性淋巴样细胞中p27kip1表达的比较评估表明,局部胃DLBL患者的B细胞表达的p27kip1最少,为0.36±0.32。该值低于患有晚期DLBL的患者的恶性淋巴细胞的0.64±0.53,晚期低度MALT淋巴瘤的1.59±0.79和局部低度MALT淋巴瘤的患者的1.59±0.84。在输入所有p27kip1变量的多变量模型中,无论疾病的阶段如何,恶性淋巴瘤细胞中p27kip1的表达均与淋巴瘤的级别呈负相关(p = 0.0001),并显着预测了级别:OR:0.07 ,95%CI 0.07–0.31,p = 0.0001。结论:p27kip1可能是区分低度和高度胃淋巴瘤的公认分子标记。

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