Wind Thijs T, Jalving Mathilde, de Haan Jacco J, de Vries Elisabeth G E, van Vugt Marcel A T M, Reijngoud Dirk-Jan, van Rijn Rozemarijn S, Haanen John B A G, Blank Christian U, Hospers Geke A P, Fehrmann Rudolf S N
Comprehensive Cancer Centre, University Medical Centre Groningen and University of Groningen, Groningen, The Netherlands.
Section of Systems Medicine and Metabolic Signaling, Laboratory of Pediatrics, Department of Pediatrics, Center of Liver, Digestive and Metabolic Diseases, University Medical Center Groningen.
Oncoimmunology. 2019 Jan 3;8(3):1558664. doi: 10.1080/2162402X.2018.1558664. eCollection 2019.
This study aimed to establish the number of expression-based molecular subclasses in cutaneous melanoma, identify their dominant biological pathways and evaluate their clinical relevance. To this end, consensus clustering was performed separately on two independent datasets (n = 405 and n = 473) composed of publicly available cutaneous melanoma expression profiles from previous studies. Four expression-based molecular subclasses were identified and labelled 'Oxidative phosphorylation', 'Oestrogen response/p53-pathway', 'Immune' and 'Cell cycle', based on their dominantly expressed biological pathways determined by gene set enrichment analysis. Multivariate survival analysis revealed shorter overall survival in the 'Oxidative phosphorylation' subclass compared to the other subclasses. This was validated in a third independent dataset (n = 214). Finally, in a pooled cohort of 76 patients treated with anti-PD-1 therapy a trend towards a difference in response rates between subclasses was observed ('Immune' subclass: 65% responders, 'Oxidative Phosphorylation' subclass: 60% responders, other subclasses: <50% responders). These findings support the stratification of cutaneous melanoma in four expression-based molecular subclasses.
本研究旨在确定皮肤黑色素瘤基于表达的分子亚类数量,识别其主要生物学途径,并评估其临床相关性。为此,对两个独立数据集(n = 405和n = 473)分别进行了一致性聚类,这两个数据集由先前研究中公开可用的皮肤黑色素瘤表达谱组成。基于基因集富集分析确定的主要表达生物学途径,识别出四个基于表达的分子亚类,并分别标记为“氧化磷酸化”、“雌激素反应/p53途径”、“免疫”和“细胞周期”。多变量生存分析显示,与其他亚类相比,“氧化磷酸化”亚类的总生存期较短。这在第三个独立数据集(n = 214)中得到了验证。最后,在一个由76例接受抗PD-1治疗的患者组成的汇总队列中,观察到亚类之间的反应率存在差异趋势(“免疫”亚类:65%有反应者,“氧化磷酸化”亚类:60%有反应者,其他亚类:<50%有反应者)。这些发现支持将皮肤黑色素瘤分为四个基于表达的分子亚类。