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FOXO3在肺癌组织与肺癌干细胞中的表达特征及其与肺癌分化转移的相关性分析 被引量:4

Expression of FOXO3 in lung cancer tissues and lung cancer stem cells and its correlation with differentiation and metastasis of lung cancer
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摘要 目的 分析FOXO3在肺癌组织与肺癌干细胞中的表达特征及其与肺癌分化转移的相关性。方法 回顾性分析105例肺癌患者的临床资料,并以35例正常肺组织标本进行对照分析。分别采用免疫组织化学法、Western blot及反转录-聚合酶链反应(RT-PCR)法对肺癌组织和正常肺组织中FOXO3的表达情况进行检测,并用Western blot和RT-PCR法对肺癌干细胞中FOXO3蛋白和mRNA表达水平进行检测,同时比较不同病理类型、分化程度及是否伴有淋巴结转移的肺癌患者FOXO3蛋白表达情况。结果 免疫组织化学法检测发现,FOXO3蛋白主要定位于细胞质和细胞间质中,且低表达于不同病理类型的肺癌组织。Western blot检测发现,肺癌组织中FOXO3蛋白表达水平较正常肺组织显著下调( P <0.01);肺癌干细胞中FOXO3蛋白表达水平较正常肺组织亦显著下调( P <0.01)。RT-PCR检测发现,肺癌组织中FOXO3 mRNA相对表达量较正常肺组织显著降低( P <0.01);肺癌干细胞中FOXO3 mRNA相对表达量较正常肺组织亦显著降低( P <0.01)。不同病理类型的肺癌患者FOXO3蛋白阳性率的比较,差异无统计学意义( P >0.05);未分化+低分化、伴有淋巴结转移的患者FOXO3蛋白阳性率较中分化+高分化、无淋巴结转移者显著降低( P <0.05)。结论 肺癌组织与肺癌干细胞中FOXO3具有低表达的特点,并且其与肺癌分化程度和淋巴结转移存在密切关系,FOXO3有望成为临床治疗肺癌患者的新型靶点,具有潜在的研究价值。 Objective To analyze the expression of FOXO3 in lung cancer tissues and lung cancer stem cells and its correlation with differentiation and metastasis of lung cancer. Methods The clinical data of 105 patients with lung cancer in our hospital were retrospectively analyzed and compared with 35 cases of normal lung tissue specimens. The expression of FOXO3 in lung cancer tissues and normal lung tissues was detected by immunohistochemistry, Western blot and reverse transcription-polymerase chain reaction (RT-PCR). The expression levels of FOXO3 protein and mRNA in lung cancer stem cells were detected by Western blot and RT-PCR. At the same time, lung cancer patients with different pathological types, differentiation degree and lymph node metastasis were compared. The expression of FOXO3 protein in the patients. Results Immunohistochemistry showed that FOXO3 protein was mainly localized in cytoplasm and interstitium, and was low expressed in lung cancer tissues of different pathological types. Western blot showed that the expression of FOXO3 in lung cancer tissues was significantly lower than that in normal lung tissues ( P <0.01). The expression of FOXO3 in lung cancer stem cells was also significantly lower than that in normal lung tissues ( P <0.01). RT-PCR showed that the relative expression of FOXO 3 in lung cancer tissues was significantly lower than that in normal lung tissues ( P <0.01). The relative expression of FOXO 3 in lung cancer stem cells was also significantly lower than that in normal lung tissues ( P <0.01). The positive rate of FOXO3 protein in lung cancer patients with different pathological types had no statistical significance ( P >0.05). The positive rate of FOXO3 protein in undifferentiated + poorly differentiated patients with lymph node metastasis was significantly lower than that in moderately differentiated + highly differentiated patients without lymph node metastasis ( P <0.05). Conclusion FOXO3 expression in lung cancer tissues and lung cancer stem cells is low, and it is closely related to the degree of differentiation and lymph node metastasis of lung cancer. It is expected to become a new target for clinical treatment of lung cancer patients and has potential research value.
作者 李莉红 梁晶 白璐 LI Li-hong;LIANG Jing;BAI Lu(Department of Geriatric Respiratory, Xi'an No. 1 People's Hospital, Xi'an Shaanxi 710002, China;Department of Radiotherapy, Shaanxi Cancer Hospital, Xi'an Shaanxi 710061, China)
出处 《临床和实验医学杂志》 2019年第14期1519-1522,共4页 Journal of Clinical and Experimental Medicine
基金 陕西省自然科学基础研究计划项目(编号:2017JM8071)
关键词 肺癌 干细胞 FOXO3 免疫组织化学法 分化 转移 Lung cancer Stem cells FOXO3 Immunohistochemistry Differentiation Metastasis
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  • 1JingLIU AnningLIN.Role of JNK activation in apoptosis:Adouble-edged sword[J].Cell Research,2005,15(1):36-42. 被引量:75
  • 2项永兵,高玉堂.非吸烟女性肺癌危险因素的多分类logistic模型分析[J].中国卫生统计,2005,22(2):66-70. 被引量:30
  • 3邹小农.中国肺癌流行病学[J].中华肿瘤防治杂志,2007,14(12):881-883. 被引量:151
  • 4王梅,魏文强.中国肺癌患者住院人次增长现况及其主要影响因素分析[J].中国肿瘤,2007,16(9):672-675. 被引量:25
  • 5Lu Xueguan,Wang Xiaoshen,Zhang Yongsheng,Hu Chaosu,Shen Chunying,Feng Yan.Hypoxia Inducible Factor-1α and Vascular Endothelial Growth Factor Expression are Associated with a Poor Prognosis in Patients with Nasopharyngeal Carcinoma Receiving Radiotherapy with Carbogen and Nicotinamide[J].Clinical Oncology.2008(8)
  • 6Liang Fang,HuiMng Wang,Lin Zhou,Da Yu.Akt-FOXO3a signaling axis dysregulation in human oral squamous cell carcinoma and potent efficacy of FOXO3a-targeted gene therapy[J]. Oral Oncology . 2010 (1)
  • 7Sanjeev Shukla,Meenakshi Shukla,Gregory MacLennan,Pingfu Fu,Sanjay Gupta.Deregulation of FOXO3A during prostate cancer progression[J]. International Journal of Oncology . 2009 (6)
  • 8Walbert J. Bakker,Isaac S. Harris,Tak W. Mak.FOXO3a Is Activated in Response to Hypoxic Stress and Inhibits HIF1-Induced Apoptosis via Regulation of CITED2[J]. Molecular Cell . 2007 (6)
  • 9Domenico Accili,Karen C Arden.FoxOs at the Crossroads of Cellular Metabolism, Differentiation, and Transformation[J]. Cell . 2004 (4)
  • 10Mickey C.-T Hu,Dung-Fang Lee,Weiya Xia,Leonard S Golfman,Fu Ou-Yang,Jer-Yen Yang,Yiyu Zou,Shilai Bao,Norihisa Hanada,Hitomi Saso,Ryuji Kobayashi,Mien-Chie Hung.IκB Kinase Promotes Tumorigenesis through Inhibition of Forkhead FOXO3a[J]. Cell . 2004 (2)

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