Berdiel-Acer Mireia, Berenguer Antoni, Sanz-Pamplona Rebeca, Cuadras Daniel, Sanjuan Xavier, Paules Maria José, Santos Cristina, Salazar Ramon, Moreno Victor, Capella Gabriel, Villanueva Alberto, Molleví David G
Translational Research Laboratory, Catalan Institute of Oncology, IDIBELL, L'Hospitalet de Llobregat, Catalonia, Spain.
Biomarkers and Susceptibility Unit, Cancer Prevention and Monitoring Programme, Catalan Institute of Oncology, IDIBELL, L'Hospitalet de Llobregat, Catalonia, Spain.
Oncotarget. 2014 Aug 15;5(15):6437-52. doi: 10.18632/oncotarget.2237.
Based on 108 differentially expressed genes between carcinoma-associated fibroblasts (CAFs) and paired normal colonic fibroblasts we recently reported, a 5-gene classifier for relapse prediction in Stage II/III colorectal cancer (CRC ) was developed. Its predictive value was validated in datasets GSE17538, GSE33113 and GSE14095. An additional validation was performed in a metacohort (n=317) and 142 CRC patients by means of RT-PCR. The 5-gene classifier was significantly associated with increased relapse risk and death from CRC across all validation series of Stage II/III patients used. Multivariate Cox regression analyses confirmed the independent prognostic value of the stromal classifier (HR=2.67; P=0.002). Post-test probabilities provided evidence of the suitability of the 5-gene classifier in clinical practice, identifying a subgroup of Stage-II patients who were at high risk of relapse. Moreover, the a priory worst prognosis mesenchymal subtype of tumours can be stratified according to the physiological status of their carcinoma-associated fibroblasts. In conclusion the CAFs-derived 5-gene classifier provides more accurate information about outcome than conventional clinicopathological criteria and it could be useful to take clinical decisions, especially in Stage II. Additionally, the classifier put into relevance the CAF's intratumoral heterogeneity and might contribute to find relevant targets for depleting adequate CAFS subtypes.
基于我们最近报道的癌相关成纤维细胞(CAFs)与配对的正常结肠成纤维细胞之间的108个差异表达基因,开发了一种用于预测II/III期结直肠癌(CRC)复发的5基因分类器。其预测价值在数据集GSE17538、GSE33113和GSE14095中得到验证。通过RT-PCR在一个meta队列(n = 317)和142例CRC患者中进行了额外验证。在所有使用的II/III期患者验证系列中,5基因分类器与CRC复发风险增加和死亡显著相关。多变量Cox回归分析证实了基质分类器的独立预后价值(HR = 2.67;P = 0.002)。检验后概率提供了5基因分类器在临床实践中适用性的证据,识别出了复发风险高的II期患者亚组。此外,肿瘤预后最差的间充质亚型可根据其癌相关成纤维细胞的生理状态进行分层。总之,源自CAFs的5基因分类器比传统的临床病理标准能提供更准确的预后信息,对临床决策可能有用,尤其是在II期。此外,该分类器揭示了CAF的肿瘤内异质性,并可能有助于找到针对消耗适当CAF亚型的相关靶点。