Grigoroiu Madalina, Tagett Rebecca, Draghici Sorin, Dima Simona, Nastase Anca, Florea Raluca, Sorop Andrei, Ilie Veronica, Bacalbasa Nicolae, Tica Valeria, Laszlo Viktoria, Mansuet-Lupo Audrey, Damotte Dianne, Klepetko Walter, Popescu Irinel, Regnard Jean Francois
Center of Digestive Diseases and Liver Transplantation, Fundeni Clinical Institute, Bucharest, Romania
Intelligent Systems and Bioinformatics Laboratory (ISBL), Department of Computer Science - Wayne State University, Detroit, MI, U.S.A.
Cancer Genomics Proteomics. 2015 Sep-Oct;12(5):231-42.
BACKGROUND/AIM: The aim of the study was to determine the pathways and expression profile of the genes that might predict response to neoadjuvant chemotherapy in patients with stage IIIA non-small cell lung cancer (NSCLC).
We evaluated, by microarray, the gene-expression profile of tumoral mediastinal lymph node samples surgically removed from 27 patients with stage IIIA NSCLC before neoadjuvant chemotherapy treatment. Depending on the response to the induction treatment, the patients were divided in two groups: group A: patients whose disease evolved, stabilized or who had minor response to chemotherapy, and group B: patients whose disease stabilized or had major response to chemotherapy.
The microarray experiments identified 1,127 genes with a modified expression in the tumoral tissue compared to normal tissue with p≤0.05 and 44 genes with p≤0.01. The identified up-regulated genes between tumoral versus normal tissue included collagen, type I, alpha 1 (COL1A1), inhibin beta A (INHBA) and thioredoxin interacting protein (TXNIP). Pathways identified with a false-discovery rate of <0.005 included: cytokine pathways, focal adhesion or extracellular matrix receptor interaction.
Our approach identified important characteristics of NSCLC and pointed-out molecular differences between sub-groups of patients based on their response to therapy.
背景/目的:本研究旨在确定可预测IIIA期非小细胞肺癌(NSCLC)患者对新辅助化疗反应的基因通路及表达谱。
我们通过微阵列评估了27例IIIA期NSCLC患者在新辅助化疗前手术切除的肿瘤纵隔淋巴结样本的基因表达谱。根据诱导治疗的反应,将患者分为两组:A组:疾病进展、稳定或对化疗反应较小的患者;B组:疾病稳定或对化疗反应较大的患者。
微阵列实验确定了1127个在肿瘤组织中表达与正常组织相比有改变且p≤0.05的基因,以及44个p≤0.01的基因。肿瘤组织与正常组织之间鉴定出的上调基因包括I型胶原α1(COL1A1)、抑制素βA(INHBA)和硫氧还蛋白相互作用蛋白(TXNIP)。错误发现率<0.005的鉴定通路包括:细胞因子通路、粘着斑或细胞外基质受体相互作用。
我们的方法确定了NSCLC的重要特征,并指出了基于患者对治疗反应的亚组之间的分子差异。