Bioinformatics and Systems Biology Program, University of California, San Diego, La Jolla, CA 92093, USA.
Blood. 2012 Sep 27;120(13):2639-49. doi: 10.1182/blood-2012-03-416461. Epub 2012 Jul 26.
The clinical course of patients with chronic lymphocytic leukemia (CLL) is heterogeneous. Several prognostic factors have been identified that can stratify patients into groups that differ in their relative tendency for disease progression and/or survival. Here, we pursued a subnetwork-based analysis of gene expression profiles to discriminate between groups of patients with disparate risks for CLL progression. From an initial cohort of 130 patients, we identified 38 prognostic subnetworks that could predict the relative risk for disease progression requiring therapy from the time of sample collection, more accurately than established markers. The prognostic power of these subnetworks then was validated on 2 other cohorts of patients. We noted reduced divergence in gene expression between leukemia cells of CLL patients classified at diagnosis with aggressive versus indolent disease over time. The predictive subnetworks vary in levels of expression over time but exhibit increased similarity at later time points before therapy, suggesting that degenerate pathways apparently converge into common pathways that are associated with disease progression. As such, these results have implications for understanding cancer evolution and for the development of novel treatment strategies for patients with CLL.
慢性淋巴细胞白血病(CLL)患者的临床病程存在异质性。已经确定了一些预后因素,可以将患者分为疾病进展和/或生存风险不同的组。在这里,我们进行了基于子网络的基因表达谱分析,以区分具有不同 CLL 进展风险的患者群体。从最初的 130 名患者队列中,我们确定了 38 个预后子网络,这些子网络可以预测从样本采集时间开始需要治疗的疾病进展的相对风险,比既定的标志物更准确。然后在另外两个患者队列中验证了这些子网的预后能力。我们注意到,随着时间的推移,诊断时分类为侵袭性和惰性疾病的 CLL 患者的白血病细胞之间的基因表达差异缩小。预测性子网的表达水平随时间变化,但在治疗前的后期时间点表现出更高的相似性,这表明退化途径显然会汇集到与疾病进展相关的共同途径中。因此,这些结果对于理解癌症进化以及为 CLL 患者开发新的治疗策略具有重要意义。