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Nitric oxide synthase type 1 expression in human lung cancer and its relation to p53.

机译:一氧化氮合酶1型在人肺癌中的表达及其与p53的关系。

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BACKGROUND: The nitric oxide synthases (NOS) have been observed in humantumour cell lines as well as in solid tumours. Neuronal isoform of NOS (NOS1) was particularly abundantin low-differentiated gynaecological, breast and central nerve system tumours, suggesting that it maycharacterize poorly differentiated tumours. So far, little is known about expression of the neuronalNOS isoform in non-small cell lung cancer. Our aim was to compare NOS1 expression in non-small lung carcinomaswith respect to tumor staging and p53 protein expression. MATERIAL AND METHODS: Thirty-two cases of non-smalllung carcinomas of all grades of malignancy and ten control lung specimens with neoplastic lesions wereexamined. Paraffin-embedded tissues were stained with hematoxylin and eosin, or with antibodies to NOS1and p53, and evaluated under light microscope. RESULTS: No statistical correlation between expressionof p53, NOS1 and degree od tumour differentiation was observed. CONCLUSION: Expression of NOS1 can notserve as a marker for highly malignant tumours in the non-small cell lung carcinomas.
机译:背景:一氧化氮合酶(NOS)已在人肿瘤细胞系和实体瘤中观察到。 NOS(NOS1)的神经元同工型在低分化妇科,乳腺和中枢神经系统肿瘤中尤为丰富,表明它可能是分化较差的肿瘤的特征。迄今为止,关于神经元NOS同工型在非小细胞肺癌中的表达知之甚少。我们的目的是比较非小细胞肺癌中NOS1表达与肿瘤分期和p53蛋白表达的关系。材料与方法:检查了32例各种级别的非小细胞肺癌患者和10例具有肿瘤性病变的对照肺标本。石蜡包埋的组织用苏木精和曙红或NOS1和p53抗体染色,并在光学显微镜下进行评估。结果:p53,NOS1的表达与肿瘤分化程度之间无统计学意义。结论:NOS1的表达不能作为非小细胞肺癌高度恶性肿瘤的标志物。

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