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不同的肺癌亚型与肿瘤进展的不同驱动因素相关。

Distinct lung cancer subtypes associate to distinct drivers of tumor progression.

作者信息

Relli Valeria, Trerotola Marco, Guerra Emanuela, Alberti Saverio

机构信息

Unit of Cancer Pathology, CeSI-MeT, University "G. d'Annunzio", Chieti, Italy.

Department of Medical, Oral and Biotechnological Sciences, University "G. d'Annunzio", Chieti, Italy.

出版信息

Oncotarget. 2018 Oct 30;9(85):35528-35540. doi: 10.18632/oncotarget.26217.

DOI:10.18632/oncotarget.26217
PMID:30473748
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6238974/
Abstract

The main non-small-cell lung cancer (NSCLC) histopathological subtypes are lung adenocarcinomas (LUAD) and lung squamous cell carcinomas (LUSC). To identify candidate progression determinants of NSCLC subtypes, we explored the transcriptomic signatures of LUAD versus LUSC. We then investigated the prognostic impact of the identified tumor-associated determinants. This was done utilizing DNA microarray data from 2,437 NSCLC patients. An independent analysis of a case series of 994 NSCLC was conducted by next-generation sequencing, together with gene expression profiling from GEO (https://www.ncbi.nlm.nih.gov/geo/). This work led us to identify 69 distinct tumor prognostic determinants, which impact on LUAD or LUSC clinical outcome. These included key drivers of tumor growth and cell cycle, transcription factors and metabolic determinants. Such disease determinants appeared vastly different in LUAD versus LUSC, and often had opposite impact on clinical outcome. These findings indicate that distinct tumor progression pathways are at work in the two NSCLC subtypes. Notably, most prognostic determinants would go inappropriately assessed or even undetected when globally investigating unselected NSCLC. Hence, differential consideration for NSCLC subtypes should be taken into account in current clinical evaluation procedures for lung cancer.

摘要

主要的非小细胞肺癌(NSCLC)组织病理学亚型是肺腺癌(LUAD)和肺鳞状细胞癌(LUSC)。为了确定NSCLC亚型的候选进展决定因素,我们探索了LUAD与LUSC的转录组特征。然后,我们研究了所确定的肿瘤相关决定因素的预后影响。这是利用来自2437例NSCLC患者的DNA微阵列数据完成的。通过下一代测序对994例NSCLC病例系列进行了独立分析,并结合了来自GEO(https://www.ncbi.nlm.nih.gov/geo/)的基因表达谱。这项工作使我们确定了69个不同的肿瘤预后决定因素,它们影响LUAD或LUSC的临床结果。这些因素包括肿瘤生长和细胞周期的关键驱动因素、转录因子和代谢决定因素。这些疾病决定因素在LUAD和LUSC中表现出很大差异,并且通常对临床结果有相反的影响。这些发现表明,两种NSCLC亚型存在不同的肿瘤进展途径。值得注意的是,在对未选择的NSCLC进行全面研究时,大多数预后决定因素可能会被不恰当地评估甚至未被发现。因此,在目前肺癌的临床评估程序中应考虑对NSCLC亚型进行区别对待。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc6/6238974/c5101d45e753/oncotarget-09-35528-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc6/6238974/f234ea7e081b/oncotarget-09-35528-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc6/6238974/7ecb09ff78db/oncotarget-09-35528-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc6/6238974/42a44c59d05a/oncotarget-09-35528-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc6/6238974/09e891aeca9c/oncotarget-09-35528-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc6/6238974/8dce3fdc88b3/oncotarget-09-35528-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc6/6238974/c5101d45e753/oncotarget-09-35528-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc6/6238974/f234ea7e081b/oncotarget-09-35528-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc6/6238974/7ecb09ff78db/oncotarget-09-35528-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc6/6238974/42a44c59d05a/oncotarget-09-35528-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc6/6238974/09e891aeca9c/oncotarget-09-35528-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc6/6238974/8dce3fdc88b3/oncotarget-09-35528-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc6/6238974/c5101d45e753/oncotarget-09-35528-g006.jpg

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