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Significance of stem cell marker Nanog gene in the diagnosis and prognosis of lung cancer

机译:干细胞标志物Nanog基因在肺癌诊断和预后中的意义

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摘要

The aim of the present study was to analyze the stem cell marker, Nanog gene, for the diagnosis and prognosis of lung cancer cases, and to study its application in the diagnosis of lung cancer. In total, 100 patients diagnosed with lung cancer between April, 2013 and May, 2015 were included in the present study. The patients were randomly divided into group A (lung cancer) and group B (squamous cell lung carcinoma). RT-PCR was used to detect the cancer and adjacent tissues, and Nanog gene expression was detected in groups A and B in cells. The results showed that, analysis of Nanog gene expression in the two groups of patients varied to different degrees. There was no significant difference between the two groups with regard to age, gender, disease stage and lymph node metastasis. Nanog gene expression in patients with carcinoma were significantly higher than that in the adjacent tissues (p<0.05). By contrast, differentiated and well-differentiated carcinoma tissue showed a significantly higher Nanog gene expression than poorly differentiated and undifferentiated carcinoma (p<0.05). The expression of Nanog in normal cells was significantly higher than that in normal lung tissues and benign lesions in lung cancer stem cells. Nanog was highly expressed in CD44+ cells, and Nanog expression in lung cancer stem cells was significantly higher (p<0.05). In conclusion, for groups A (lung cancer) and B (squamous cell lung carcinoma) the Nanog gene expression was significantly higher. The data of the present study show that the patients with stage III and IV lung cancer had a higher Nanog gene expression. In addition, there was a higher expression of Nanog in lung cancer patients. By contrast, a lower degree of cell differentiation was associated with strong Nanog gene expression in lung cancer.
机译:本研究的目的是分析干细胞标记物Nanog基因,以诊断和预后肺癌病例,并研究其在肺癌诊断中的应用。本研究共纳入2013年4月至2015年5月之间100例被诊断为肺癌的患者。将患者随机分为A组(肺癌)和B组(鳞状细胞肺癌)。使用RT-PCR检测癌症和邻近组织,并在细胞的A和B组中检测Nanog基因表达。结果表明,两组患者Nanog基因表达的分析程度不同。两组在年龄,性别,疾病阶段和淋巴结转移方面无显着差异。癌组织中Nanog基因的表达明显高于癌旁组织(p <0.05)。相比之下,分化和分化程度高的癌组织比分化程度低和未分化的癌组织显着更高的Nanog基因表达(p <0.05)。 Nanog在正常细胞中的表达明显高于正常肺组织和肺癌干细胞的良性病变。 Nanog在CD44 + 细胞中高表达,在肺癌干细胞中Nanog表达显着升高(p <0.05)。总之,对于A组(肺癌)和B组(鳞状细胞肺癌),Nanog基因表达明显更高。本研究的数据表明,III和IV期肺癌患者具有更高的Nanog基因表达。另外,在肺癌患者中Nanog的表达更高。相比之下,较低的细胞分化程度与肺癌中强大的Nanog基因表达有关。

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