Walter Robert Fred Henry, Werner Robert, Ting Saskia, Vollbrecht Claudia, Theegarten Dirk, Christoph Daniel Christian, Schmid Kurt Werner, Wohlschlaeger Jeremias, Mairinger Fabian Dominik
Ruhrlandklinik, West German Lung Center, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
Institute of Pathology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
Oncotarget. 2015 Sep 22;6(28):24690-8. doi: 10.18632/oncotarget.3992.
Neuroendocrine tumors of the lung comprise typical (TC) and atypical carcinoids (AC), large-cell neuroendocrine cancer (LCNEC) and small-cell lung cancer (SCLC). Cell cycle and apoptosis are key pathways of multicellular homeostasis and deregulation of these pathways is associated with cancerogenesis.
Sixty representative FFPE-specimens (16 TC, 13 AC, 16 LCNEC and 15 SCLC) were used for mRNA expression analysis using the NanoString technique. Eight genes related to apoptosis and ten genes regulating key points of cell cycle were investigated.
ASCL1, BCL2, CASP8, CCNE1, CDK1, CDK2, CDKN1A and CDKN2A showed lower expression in carcinoids compared to carcinomas. In contrast, CCNE1 and CDK6 showed elevated expression in carcinoids compared to carcinomas. The calculated BCL2/BAX ratio showed increasing values from TC to SCLC. Between SCLC and LCNEC CDK2, CDKN1B, CDKN2A and PNN expression was significantly different with higher expression in SCLC.
Carcinoids have increased CDK4/6 and CCND1 expression controlling RB1 phosphorylation via this signaling cascade. CDK2 and CCNE1 were increased in carcinomas showing that these use the opposite way to control RB1. BAX and BCL2 are antagonists in regulating apoptosis. BCL2 expression increased over BAX expression with increasing malignancy of the tumor from TC to SCLC.
肺神经内分泌肿瘤包括典型类癌(TC)、非典型类癌(AC)、大细胞神经内分泌癌(LCNEC)和小细胞肺癌(SCLC)。细胞周期和凋亡是多细胞稳态的关键途径,这些途径的失调与肿瘤发生相关。
使用NanoString技术对60个代表性的福尔马林固定石蜡包埋标本(16个TC、13个AC、16个LCNEC和15个SCLC)进行mRNA表达分析。研究了8个与凋亡相关的基因和10个调节细胞周期关键点的基因。
与癌相比,ASCL1、BCL2、CASP8、CCNE1、CDK1、CDK2、CDKN1A和CDKN2A在类癌中的表达较低。相比之下,与癌相比,CCNE1和CDK6在类癌中的表达升高。计算得出的BCL2/BAX比值从TC到SCLC呈增加趋势。在SCLC和LCNEC之间,CDK2、CDKN1B、CDKN2A和PNN的表达存在显著差异,在SCLC中表达更高。
类癌通过该信号级联增加了CDK4/6和CCND1的表达,从而控制RB1磷酸化。CDK2和CCNE1在癌中增加,表明它们通过相反的方式控制RB1。BAX和BCL2是调节凋亡的拮抗剂。随着肿瘤从TC到SCLC恶性程度的增加,BCL2的表达相对于BAX的表达增加。