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C/EBPα在肺癌中的下调及抗增殖作用

Down-regulation and antiproliferative role of C/EBPalpha in lung cancer.

作者信息

Halmos Balazs, Huettner Claudia S, Kocher Olivier, Ferenczi Katalin, Karp Daniel D, Tenen Daniel G

机构信息

Division of Hematology/Oncology, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215, USA.

出版信息

Cancer Res. 2002 Jan 15;62(2):528-34.

Abstract

The transcription factor, CCAAT/enhancer binding protein alpha (C/EBPalpha) is important in the terminal differentiation of granulocytes, hepatocytes, and adipocytes, and recurrent mutations of C/EBPalpha were described in acute myeloid leukemia. In the lung, C/EBPalpha is expressed in bronchial cells and type II pneumocytes. Abnormal proliferation of the latter cell type was reported in C/EBPalpha knockout mice. We determined the expression of C/EBPalpha by Northern blot analysis in 30 lung cancer cell lines and found significant down-regulation in 24 cell lines. Immunohistochemical study of primary tumor specimens showed undetectable or low expression of C/EBPalpha in 23 of 53 specimens. Its expression was more frequently down-regulated in adenocarcinoma and poorly differentiated cancer specimens than in squamous cell cancers. A higher frequency of reduced expression was found in more advanced stages. To investigate the consequences of C/EBPalpha expression in lung cancer cells, we stably transfected two cell lines that do not express the gene (Calu1 and H358) with a plasmid allowing for induction of C/EBPalpha protein expression. Induction of C/EBPalpha led to significant growth reduction attributable to proliferation arrest, morphological changes characteristic of differentiation, and apoptosis. These results suggest that C/EBPalpha is down-regulated in a large proportion of lung cancers and that it has growth-inhibitory properties in airway epithelial cells. Genetic analysis of the C/EBPalpha gene is in progress to fully evaluate its role as a novel tumor suppressor in lung cancer.

摘要

转录因子CCAAT/增强子结合蛋白α(C/EBPα)在粒细胞、肝细胞和脂肪细胞的终末分化中起重要作用,急性髓系白血病中已报道C/EBPα存在反复突变。在肺中,C/EBPα在支气管细胞和II型肺细胞中表达。据报道,在C/EBPα基因敲除小鼠中,后一种细胞类型出现异常增殖。我们通过Northern印迹分析确定了30种肺癌细胞系中C/EBPα的表达情况,发现24种细胞系中存在显著下调。对原发性肿瘤标本的免疫组织化学研究显示,53份标本中有23份检测不到或低表达C/EBPα。与鳞状细胞癌相比,腺癌和低分化癌标本中其表达更频繁下调。在更晚期阶段,表达降低的频率更高。为了研究C/EBPα在肺癌细胞中的表达后果,我们用一种可诱导C/EBPα蛋白表达的质粒稳定转染了两种不表达该基因的细胞系(Calu1和H358)。C/EBPα的诱导导致显著的生长抑制,这归因于增殖停滞、分化特征性的形态变化和细胞凋亡。这些结果表明,C/EBPα在大部分肺癌中表达下调,并且在气道上皮细胞中具有生长抑制特性。目前正在对C/EBPα基因进行遗传分析,以全面评估其作为肺癌新型肿瘤抑制因子的作用。

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