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Immunohistochemical expression and significance of NM23 suppressor protein in primary gastric adenocarcinoma

机译:NM23抑制蛋白在原发性胃腺癌中的免疫组织化学表达及意义

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摘要

NM 23 protein was originally identified as a metastasis suppressor protein. The expression of NM23 has been correlated with tumour metastatic potential in various human carcinoma, mostly in ductal breast and colorectal carcinomas. Evidence for their expression in gastric cancer is rather contradictory, both for protein expression status and prognostic vale. This study was done to analyze the immunohistochemical expression of NM23 in gastric carcinoma, and correlation of the degree of staining with clinicopathological parameters was investigated.In a retrospective immunohistochemical study specimens obtained from 56 gastric cancer patients who had undergone gastrectomy with perigastric lymphadenectomy were analysed, in correlation with classical clinical-pathological parameters of tumours, WHO-, Lauren-, Goseki-, and Ming- classification. NM 23 gene expression was compared in gastric adenocarcinoma and tumour-adjacent non-neoplastic gastric mucosa. A semiquantitative immunostaining evaluation (score 0-3) was used, counting the percentage of stained cells. Statistical analysis was performed using Kolmogorov-Smirnov test, and Spearman rank correlation test.The investigated group consisted of 40 males and 16 females (2.5:1) with a mean age of 63 years (range: 48-81 years). The percentage of positive expression of NM23 (score 3) were in 30 (53.5%) specimens in non-neoplastic mucosa in adjacent gastric carcinoma, and negative (score 0-2) in all 56 (100%) specimens of gastric adenocarcinoma. NM23 expression was higher in non-neoplastic mucosa than in adjacent gastric adenocarcinoma tissue (p<0.0001). NM23 protein expression did not correlate with gender (p=0.115), tumour size (p=0.844), tumour grade (p>=0.172), lymphovascular invasion (p=0.606), lymph node metastases (p=0.311), Lauren classification (p=0.426), Goseki classification (p=0.458) and Ming classification (p=0.212).Our series did not show a significant correlation between NM23 expression and analysed clinico-pathological variables, but these results suggest that protein NM23 may have a role in gastric carcinoma pathogenesis.
机译:NM 23蛋白最初被鉴定为转移抑制蛋白。 NM23的表达已与各种人类癌症,主要在乳腺导管癌和结肠直肠癌中的转移潜力相关联。无论在蛋白质表达状态还是预后方面,它们在胃癌中表达的证据都相矛盾。本研究旨在分析NM23在胃癌中的免疫组织化学表达,并探讨其染色程度与临床病理参数的相关性。在一项回顾性免疫组织化学研究中,分析了56例经胃切除术并经胃周淋巴结切除术的胃癌患者的样本,与经典的肿瘤临床病理参数,WHO-,Lauren-,Goseki-和Ming-分类相关。比较了NM 23基因在胃腺癌和与肿瘤相邻的非肿瘤性胃黏膜中的表达。使用半定量免疫染色评估(评分0-3),计算染色细胞的百分比。采用Kolmogorov-Smirnov检验和Spearman秩相关检验进行统计分析。研究组由40名男性和16名女性(2.5:1)组成,平均年龄为63岁(范围:48-81岁)。在邻近胃癌的非肿瘤性粘膜中,有30例(53.5%)标本中NM23阳性表达的百分比(53.5%),在所有56例(100%)胃腺癌标本中NM23的阳性表达百分比(0-2分)。非肿瘤性粘膜中的NM23表达高于邻近的胃腺癌组织(p <0.0001)。 NM23蛋白表达与性别(p = 0.115),肿瘤大小(p = 0.844),肿瘤等级(p> = 0.172),淋巴管浸润(p = 0.606),淋巴结转移(p = 0.311),Lauren分类无关(p = 0.426),Goseki分类(p = 0.458)和Ming分类(p = 0.212)。我们的系列未显示NM23表达与分析的临床病理变量之间有显着相关性,但这些结果表明NM23蛋白可能具有在胃癌发病机理中的作用。

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