Li Ping, Zhang Lei, Yu Xuexin, Tong Run, Di Xuebing, Mao Yousheng, Gao Yanning, Zhang Kaitai, Feng Lin, Cheng Shujun
State Key Laboratory of Molecular Oncology, Department of Etiology and Carcinogenesis, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Department of Endoscopy, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Cancer Sci. 2018 Feb;109(2):308-316. doi: 10.1111/cas.13456. Epub 2017 Dec 27.
There are many similarities between embryonic development and tumorigenesis, and gene expression profiles show that certain correlations exist between the gene signature during development and the clinical phenotypes of different cancers. Our group previously reported the gene expression profiles of human lung development, and the expression of one group of proliferation-related genes (PTN1 genes) steadily decreased during lung development. Here, we examined the prognostic value of PTN1 genes in 5 independent lung adenocarcinoma (ADC) and 5 lung independent squamous cell carcinoma (SCC) microarray datasets and found that the expression levels of PTN1 genes were associated with survival in lung ADC but not lung SCC. All of the lung ADC datasets contained a set of highly correlated genes from PTN1 genes, but the lung SCC datasets had no similar set of genes. We identified 63 unique core genes from the PTN1 genes in the 5 lung ADC datasets: 17 of these core genes appeared in at least 4 of the lung ADC datasets, and the 17 corresponding proteins clearly interacted more strongly with each other in lung ADC than in lung SCC. Moreover, 16 of the 17 core genes play major roles in the G /M phase of the cell cycle. These data indicate that proliferation-related genes in lung development have a significant prognostic value for lung ADC; the synergistic effects of the 17 core genes play an important role in lung ADC prognosis. These genes may have significant clinical implications for the treatment and prognosis of lung ADC.
胚胎发育与肿瘤发生之间存在许多相似之处,基因表达谱显示发育过程中的基因特征与不同癌症的临床表型之间存在一定的相关性。我们小组之前报道了人类肺发育的基因表达谱,并且一组增殖相关基因(PTN1基因)在肺发育过程中表达稳步下降。在此,我们检测了PTN1基因在5个独立的肺腺癌(ADC)和5个独立的肺鳞状细胞癌(SCC)微阵列数据集中的预后价值,发现PTN1基因的表达水平与肺ADC的生存率相关,但与肺SCC无关。所有肺ADC数据集都包含一组与PTN1基因高度相关的基因,但肺SCC数据集没有类似的基因集。我们在5个肺ADC数据集中从PTN1基因中鉴定出63个独特的核心基因:其中17个核心基因至少出现在4个肺ADC数据集中,并且这17种相应的蛋白质在肺ADC中彼此之间的相互作用明显比在肺SCC中更强。此外,17个核心基因中的16个在细胞周期的G/M期起主要作用。这些数据表明,肺发育中的增殖相关基因对肺ADC具有显著的预后价值;17个核心基因的协同作用在肺ADC预后中起重要作用。这些基因可能对肺ADC的治疗和预后具有重要的临床意义。