首页> 外文期刊>World Journal of Gastroenterology >Inducible nitric oxide synthase, nitrotyrosine and apoptosis in gastric adenocarcinomas and their correlation with a poor survival.
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Inducible nitric oxide synthase, nitrotyrosine and apoptosis in gastric adenocarcinomas and their correlation with a poor survival.

机译:胃腺癌中诱导型一氧化氮合酶,硝基酪氨酸和细胞凋亡及其与不良生存的相关性。

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AIM: To detect the presence of inducible nitric oxide synthase (iNOS), nitrotyrosine (NT) and apoptosis in gastric adenocarcinomas and their possible correlations with the clinicopathological characteristics and prognosis of gastric adenocarcinoma. METHODS: Sixty-six specimens of gastric adenocarcinoma and corresponding adjacent normal gastric tissues were studied. Immunohistochemistry was employed to localize iNOS and NT protein and an immunohistochemical scoring system was used. The occurrence of apoptotic cell death (apoptotic index (AI)) was analyzed by the terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate biotin nick-end labeling (TUNEL) method. RESULTS: Results showed that iNOS expression was detected at an intermediate or high level in 41 of 66 (62%) specimens of gastric adenocarcinoma. NT expression was 58%. Neither of them was found in the normal gastric tissues; there were significant positive correlations among iNOS expression, NT expression and AI. Many clinicopathologic characteristics of gastric adenocarcinoma, such as tumor size, depth of invasion, lymph node metastasis and TNM staging, were related to iNOS and NT expressions (P<0.05). In 66 surviving patients, the 5-year survival rate of 41 patients who had tumors with intermediate or high iNOS expressions and high AIs (4.09%; 19.96%) was significantly lower than that of 25 patients who had tumors with negative or low iNOS expressions and low AIs (0.79%; 47.14%) (P = 0.001). COX's multivariate analysis revealed that the iNOS expression was identified as one of the significant independent prognostic factors predictive of a poor survival (relative risk (RR) = 2.69). CONCLUSION: NO produced by iNOS may play a stronger role in promoting gastric adenocarcinoma growth than in suppressing its growth. iNOS and NT expressions by gastric adenocarcinoma may correlate with a poor survival.
机译:目的:检测胃腺癌中可诱导型一氧化氮合酶(iNOS),硝基酪氨酸(NT)和细胞凋亡的存在及其与胃腺癌的临床病理特征和预后的关系。方法:对66例胃腺癌及相应的邻近正常胃组织标本进行了研究。免疫组织化学用于定位iNOS和NT蛋白,并使用免疫组织化学评分系统。通过末端脱氧核苷酸转移酶介导的三磷酸脱氧尿苷生物素缺口末端标记(TUNEL)方法分析了凋亡细胞死亡(凋亡指数(AI))的发生。结果:结果显示,在66例(62%)胃腺癌样本中有41例中或高水平检测到iNOS表达。 NT表达为58%。在正常胃组织中均未发现它们。 iNOS,NT和AI之间存在显着的正相关。胃腺癌的许多临床病理特征,如肿瘤大小,浸润深度,淋巴结转移和TNM分期,均与iNOS和NT表达有关(P <0.05)。在66例幸存患者中,iNOS表达中等或较高且AI高的41例患者的5年生存率(4.09%; 19.96%)显着低于iNOS表达阴性或低水平的25例患者的5年生存率。和低AI(0.79%; 47.14%)(P = 0.001)。 COX的多变量分析显示,iNOS表达被确定为可预测生存不良的重要独立预后因素之一(相对风险(RR)= 2.69)。结论:iNOS产生的NO可能在促进胃腺癌生长方面比在抑制其生长方面发挥更强的作用。胃腺癌中iNOS和NT的表达可能与生存不良有关。

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