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基因表达模式揭示了结直肠癌中分子异质性的新层次。

Gene expression patterns unveil a new level of molecular heterogeneity in colorectal cancer.

机构信息

Bioinformatics Core Facility, Swiss Institute of Bioinformatics (SIB), Lausanne, Switzerland.

出版信息

J Pathol. 2013 Sep;231(1):63-76. doi: 10.1002/path.4212. Epub 2013 Jul 8.

Abstract

The recognition that colorectal cancer (CRC) is a heterogeneous disease in terms of clinical behaviour and response to therapy translates into an urgent need for robust molecular disease subclassifiers that can explain this heterogeneity beyond current parameters (MSI, KRAS, BRAF). Attempts to fill this gap are emerging. The Cancer Genome Atlas (TGCA) reported two main CRC groups, based on the incidence and spectrum of mutated genes, and another paper reported an EMT expression signature defined subgroup. We performed a prior free analysis of CRC heterogeneity on 1113 CRC gene expression profiles and confronted our findings to established molecular determinants and clinical, histopathological and survival data. Unsupervised clustering based on gene modules allowed us to distinguish at least five different gene expression CRC subtypes, which we call surface crypt-like, lower crypt-like, CIMP-H-like, mesenchymal and mixed. A gene set enrichment analysis combined with literature search of gene module members identified distinct biological motifs in different subtypes. The subtypes, which were not derived based on outcome, nonetheless showed differences in prognosis. Known gene copy number variations and mutations in key cancer-associated genes differed between subtypes, but the subtypes provided molecular information beyond that contained in these variables. Morphological features significantly differed between subtypes. The objective existence of the subtypes and their clinical and molecular characteristics were validated in an independent set of 720 CRC expression profiles. Our subtypes provide a novel perspective on the heterogeneity of CRC. The proposed subtypes should be further explored retrospectively on existing clinical trial datasets and, when sufficiently robust, be prospectively assessed for clinical relevance in terms of prognosis and treatment response predictive capacity. Original microarray data were uploaded to the ArrayExpress database (http://www.ebi.ac.uk/arrayexpress/) under Accession Nos E-MTAB-990 and E-MTAB-1026.

摘要

结直肠癌(CRC)在临床行为和对治疗的反应方面是一种异质性疾病,这一认识转化为迫切需要强大的分子疾病分类器,这些分类器可以解释超越当前参数(MSI、KRAS、BRAF)的异质性。填补这一空白的尝试正在出现。癌症基因组图谱(TCGA)根据基因突变的发生率和谱报道了两个主要的 CRC 组,另一篇论文报道了一个 EMT 表达特征定义的亚组。我们对 1113 个 CRC 基因表达谱进行了无先验的 CRC 异质性分析,并将我们的发现与已建立的分子决定因素以及临床、组织病理学和生存数据进行了比较。基于基因模块的无监督聚类使我们能够区分至少五个不同的 CRC 基因表达亚型,我们称之为表面隐窝样、下隐窝样、CIMP-H 样、间质样和混合样。基因集富集分析结合对基因模块成员的文献检索,确定了不同亚型中不同的生物学基序。这些亚型不是基于结果得出的,但在预后方面存在差异。已知的基因拷贝数变化和关键癌症相关基因的突变在不同亚型之间存在差异,但这些亚型提供了超出这些变量包含的分子信息。亚型之间的形态特征显著不同。在一个独立的 720 个 CRC 表达谱数据集上验证了亚型的客观存在及其临床和分子特征。我们的亚型为 CRC 的异质性提供了一个新的视角。所提出的亚型应在现有的临床试验数据集上进行回顾性探索,并且在足够稳健时,应前瞻性评估其在预后和治疗反应预测能力方面的临床相关性。原始微阵列数据已上传至 ArrayExpress 数据库(http://www.ebi.ac.uk/arrayexpress/),登录号为 E-MTAB-990 和 E-MTAB-1026。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/493a/3840702/7efdfd89f340/path0231-0063-f4.jpg

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