Towards a Genetic-Based Classification of Human Lung Cancer

I. Petersen, S. Petersen
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引用次数: 56

Abstract

Lung cancer is a highly aggressive neoplasm which is reflected by a multitude of genetic aberrations being detectable on the chromosomal and molecular level. In order to understand this seemingly genetic chaos, we performed Comparative Genomic Hybridisation (CGH) in a large collective of human lung carcinomas investigating different tumor entities as well as multiple individual tumour specimens of single patients. Despite the considerable genetic instability being reflected by the well known morphological heterogeneity of lung cancer the comparison of different tumour groups using custom made computer software revealed recurrent aberration patterns and highlighted chromosomal imbalances that were significantly associated with morphological histotypes and biological phenotypes. Specifically we identified imbalances in NSCLC being associated with metastasis formation which are typically present in SCLC thus explaining why the latter is such an aggressive neoplasm characterized by widespread tumor dissemination. Based on the genetic data a new model for the development of SCLC is presented. It suggests that SCLC evolving from the same stem cell as NSCLC should be differentiated into primary and secondary tumors. Primary SCLC corresponding to the classical type evolved directly from an epithelial precursor cell. In contrast, secondary SCLC correlating with the combined SCLC develops via an NSCLC intermediate. In addition, we established libraries of differentially expressed genes from different human lung cancer types to identify new candidate genes for several of the chromosomal subregions identified by CGH. In this review, we summarise the status of our results aiming at a refined classification of lung cancer based on the pattern of genetic aberrations.
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人类肺癌的基因分类研究
肺癌是一种高度侵袭性的肿瘤,在染色体和分子水平上可以检测到大量的遗传畸变。为了理解这种表面上的遗传混乱,我们在一个大的人类肺癌群体中进行了比较基因组杂交(CGH),研究不同的肿瘤实体以及单个患者的多个个体肿瘤标本。尽管众所周知的肺癌的形态异质性反映了相当大的遗传不稳定性,但使用定制的计算机软件对不同肿瘤组进行比较,发现了复发性畸变模式,并突出了与形态组织型和生物学表型显著相关的染色体不平衡。具体来说,我们发现非小细胞肺癌的失衡与转移形成有关,而转移形成通常存在于小细胞肺癌中,从而解释了为什么后者是一种具有广泛肿瘤播散特征的侵袭性肿瘤。基于遗传数据,提出了小细胞肺癌发展的新模式。提示SCLC与NSCLC由相同的干细胞进化而来,应区分为原发性和继发性肿瘤。与经典型相对应的原发性SCLC直接从上皮前体细胞进化而来。相比之下,继发性小细胞肺癌与合并的小细胞肺癌是通过NSCLC中间体发展的。此外,我们建立了来自不同人类肺癌类型的差异表达基因文库,以确定CGH鉴定的几个染色体亚区的新候选基因。在这篇综述中,我们总结了我们的研究结果的现状,旨在基于遗传畸变模式的肺癌精细分类。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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