Szablewski Vanessa, Bret Caroline, Kassambara Alboukadel, Devin Julie, Cartron Guillaume, Costes-Martineau Valérie, Moreaux Jérôme
University of Montpellier, UFR de Médecine, Montpellier, France.
Department of Biopathology, CHU Montpellier, Montpellier, France.
Oncotarget. 2018 Apr 10;9(27):19079-19099. doi: 10.18632/oncotarget.24901.
Diffuse large B-cell lymphoma (DLBCL) is the most common form of lymphoma and shows considerable clinical and biological heterogeneity. Much research is currently focused on the identification of prognostic markers for more specific patients' risk stratification and on the development of therapeutic approaches to improve the long-term outcome. Epigenetic alterations are involved in various cancers, including lymphoma. Interestingly, epigenetic alterations are reversible and drugs to target some of them have been developed. In this study, we demonstrated that the gene expression profile of epigenetic regulators has a prognostic value in DLBCL and identified pathways that could be involved in DLBCL poor outcome. We then designed a new risk score (EpiScore) based on the gene expression level of the epigenetic regulators DNMT3A, DOT1L, SETD8. EpiScore was predictive of overall survival in DLBCL and allowed splitting patients with DLBCL from two independent cohorts ( 414 and 69) in three groups (high, intermediate and low risk). EpiScore was an independent predictor of survival when compared with previously described prognostic factors, such as the International Prognostic Index (IPI), germinal center B cell and activated B cell molecular subgroups, gene expression-based risk score (GERS) and DNA repair score. Immunohistochemistry analysis of DNMT3A in 31 DLBCL samples showed that DNMT3A overexpression (>42% of positive tumor cells) correlated with reduced overall and event-free survival. Finally, an HDAC gene signature was significantly enriched in the DLBCL samples included in the EpiScore high-risk group. We conclude that EpiScore identifies high-risk patients with DLBCL who could benefit from epigenetic therapy.
弥漫性大B细胞淋巴瘤(DLBCL)是淋巴瘤最常见的形式,具有显著的临床和生物学异质性。目前许多研究集中于识别用于更精准患者风险分层的预后标志物,以及开发改善长期预后的治疗方法。表观遗传改变参与包括淋巴瘤在内的多种癌症。有趣的是,表观遗传改变是可逆的,并且针对其中一些改变的药物已经研发出来。在本研究中,我们证明表观遗传调节因子的基因表达谱在DLBCL中具有预后价值,并确定了可能与DLBCL不良预后相关的通路。然后,我们基于表观遗传调节因子DNMT3A、DOT1L、SETD8的基因表达水平设计了一个新的风险评分(EpiScore)。EpiScore可预测DLBCL患者的总生存期,并能将来自两个独立队列(414例和69例)的DLBCL患者分为三组(高、中、低风险)。与先前描述的预后因素(如国际预后指数(IPI)、生发中心B细胞和活化B细胞分子亚组、基于基因表达的风险评分(GERS)和DNA修复评分)相比,EpiScore是生存期的独立预测因子。对31例DLBCL样本进行的DNMT3A免疫组织化学分析表明,DNMT3A过表达(>42%的肿瘤细胞阳性)与总生存期和无事件生存期降低相关。最后,EpiScore高风险组的DLBCL样本中显著富集了一个HDAC基因特征。我们得出结论,EpiScore可识别可能从表观遗传治疗中获益的高危DLBCL患者。