Litvinov Ivan V, Tetzlaff Michael T, Thibault Philippe, Gangar Pamela, Moreau Linda, Watters Andrew K, Netchiporouk Elena, Pehr Kevin, Prieto Victor G, Rahme Elham, Provost Nathalie, Gilbert Martin, Sasseville Denis, Duvic Madeleine
Division of Dermatology, Ottawa Hospital Research Institute, University of Ottawa, Ottawa, ON, Canada.
Department of Pathology, Section of Dermatopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Oncoimmunology. 2017 Mar 17;6(5):e1306618. doi: 10.1080/2162402X.2017.1306618. eCollection 2017.
Cutaneous T-Cell Lymphomas (CTCL) are rare, but potentially devastating malignancies, whose pathogenesis remains poorly elucidated. Unfortunately, currently it is not possible to predict based on the available criteria in which patients the cancer will progress and which patients will experience an indolent disease course. Furthermore, at early stages this malignancy often masquerades as psoriasis, chronic eczema or other benign inflammatory dermatoses. As a result, it takes on average 6 y to diagnose this lymphoma since its initial presentation. In this study, we performed transcription expression profiling using TruSeq targeted RNA gene expression on 181 fresh and formalin-fixed and paraffin-embedded (FFPE) skin samples from CTCL patients and patients affected by benign inflammatory dermatoses that often mimic CTCL clinically and on histology (e.g., psoriasis, chronic eczema, etc.) We also analyzed multiple longitudinal biopsies that were obtained from the same patients over time. Our results underscore significant molecular heterogeneity with respect to gene expression between different patients and even within the same patients over time. Our study also confirmed and genes as being differentially expressed between CTCL and benign skin biopsies. In addition, we found that differential expression for a subset of these markers (e.g., and ) may be useful in prognosticating this disease. This research, combined with other molecular analyses, prepares the foundation for the development of personalized molecular approach toward diagnosis and management of CTCL.
皮肤T细胞淋巴瘤(CTCL)虽罕见,但却是具有潜在毁灭性的恶性肿瘤,其发病机制仍未完全阐明。不幸的是,目前根据现有标准无法预测哪些患者的癌症会进展,哪些患者会经历惰性病程。此外,在早期阶段,这种恶性肿瘤常伪装成银屑病、慢性湿疹或其他良性炎症性皮肤病。因此,自首次出现症状起,平均需要6年时间才能诊断出这种淋巴瘤。在本研究中,我们使用TruSeq靶向RNA基因表达技术对181份来自CTCL患者以及临床上和组织学上常模仿CTCL的良性炎症性皮肤病患者(如银屑病、慢性湿疹等)的新鲜、福尔马林固定石蜡包埋(FFPE)皮肤样本进行了转录表达谱分析。我们还分析了随时间从同一患者获取的多次纵向活检样本。我们的结果强调了不同患者之间甚至同一患者随时间变化在基因表达方面存在显著的分子异质性。我们的研究还证实了某些基因在CTCL和良性皮肤活检样本之间存在差异表达。此外,我们发现这些标志物中的一部分(如某些基因)的差异表达可能有助于预测这种疾病。这项研究与其他分子分析相结合,为开发针对CTCL诊断和管理的个性化分子方法奠定了基础。