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肺鳞状细胞癌中低 DNA 甲基化表型及其与特发性肺纤维化和预后较差的关系。

A low DNA methylation epigenotype in lung squamous cell carcinoma and its association with idiopathic pulmonary fibrosis and poorer prognosis.

机构信息

Department of General Thoracic Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.

Department of Molecular Oncology, Graduate School of Medicine, Chiba University, Chiba, Japan.

出版信息

Int J Cancer. 2020 Jan 15;146(2):388-399. doi: 10.1002/ijc.32532. Epub 2019 Jul 8.

Abstract

Patients with idiopathic pulmonary fibrosis (IPF) have higher risk of developing lung cancer, for example, squamous cell carcinoma (SCC), and show poor prognosis, while the molecular basis has not been fully investigated. Here we conducted DNA methylome analysis of lung SCC using 20 SCC samples with/without IPF, and noncancerous lung tissue samples from smokers/nonsmokers, using Infinium HumanMethylation 450K array. SCC was clustered into low- and high-methylation epigenotypes by hierarchical clustering analysis. Genes hypermethylated in SCC significantly included genes targeted by polycomb repressive complex in embryonic stem cells, and genes associated with Gene Ontology terms, for example, "transcription" and "cell adhesion," while genes hypermethylated specifically in high-methylation subgroup significantly included genes associated with "negative regulation of growth." Low-methylation subgroup significantly correlated with IPF (78%, vs. 17% in high-methylation subgroup, p = 0.04), and the correlation was validated by additional Infinium analysis of SCC samples (n = 44 in total), and data from The Cancer Genome Atlas (n = 390). The correlation between low-methylation subgroup and IPF was further validated by quantitative methylation analysis of marker genes commonly hypermethylated in SCC (HOXA2, HOXA9 and PCDHGB6), and markers specifically hypermethylated in high-methylation subgroup (DLEC1, CFTR, MT1M, CRIP3 and ALDH7A1) in 77 SCC cases using pyrosequencing (p = 0.003). Furthermore, low-methylation epigenotype significantly correlated with poorer prognosis among all SCC patients, or among patients without IPF. Multivariate analysis showed that low-methylation epigenotype is an independent predictor of poor prognosis. These may suggest that lung SCC could be stratified into molecular subtypes with distinct prognosis, and low-methylation lung SCC that significantly correlates with IPF shows unfavorable outcome.

摘要

特发性肺纤维化(IPF)患者发生肺癌的风险较高,例如鳞状细胞癌(SCC),且预后较差,但分子基础尚未完全阐明。在这里,我们使用 20 例伴有/不伴有 IPF 的 SCC 样本、吸烟者/不吸烟者的非癌性肺组织样本,通过 Infinium HumanMethylation 450K 阵列进行了 SCC 的 DNA 甲基化组分析。通过层次聚类分析将 SCC 聚类为低甲基化和高甲基化表型。在 SCC 中高甲基化的基因显著包括多梳抑制复合物在胚胎干细胞中的靶基因,以及与基因本体论术语相关的基因,例如“转录”和“细胞粘附”,而在高甲基化亚组中特异性高甲基化的基因显著包括与“生长的负调控”相关的基因。低甲基化亚组与 IPF 显著相关(78%,而高甲基化亚组为 17%,p=0.04),并通过对 SCC 样本(总共有 44 例)的额外 Infinium 分析和来自癌症基因组图谱(TCGA)(n=390)的数据进行了验证。在 77 例 SCC 病例中,通过对通常在 SCC 中高甲基化的标记基因(HOXA2、HOXA9 和 PCDHGB6)以及在高甲基化亚组中特异性高甲基化的标记基因(DLEC1、CFTR、MT1M、CRIP3 和 ALDH7A1)进行定量甲基化分析,进一步验证了低甲基化亚组与 IPF 之间的相关性(p=0.003)。此外,低甲基化表型与所有 SCC 患者或无 IPF 患者的预后较差显著相关。多变量分析显示,低甲基化表型是预后不良的独立预测因子。这可能表明,肺 SCC 可以分为具有不同预后的分子亚型,与 IPF 显著相关的低甲基化肺 SCC 预后不良。

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