Department of Comparative Biomedicine and Food Science, University of Padova , Legnaro , Italy.
Front Vet Sci. 2016 Aug 31;3:77. doi: 10.3389/fvets.2016.00077. eCollection 2016.
Diffuse large B-cell lymphoma (DLBCL) is the most common canine aggressive B-cell lymphoma worldwide, and new recent molecular approaches have shown that DLBCL constitutes a heterogeneous tumor that cannot be unraveled by morphology and immunophenotype. DLBCL behaves aggressively, typically progressing over a short period of time, and the therapy response may be difficult to be predicted. Recently, the rate of bone marrow infiltration by flow cytometry has been demonstrated to be prognostic, but more sensible markers are needed. As the clinical behavior is different, there is vast clinical and basic research devoted to identifying prognostically or biologically distinct DLBCL subgroups. Transcriptomic analysis by gene expression profile, copy number variations by array comparative genomic hybridization and epigenetic perturbations have tentatively described this heterogeneity. Molecular subgroups using oncogenic pathways and target genes have also been correlated to different outcome in a small number of cases. The objectives of this review are to summarize the current knowledge on the biology, clinical, and pathological characteristics of canine DLBCL. To date, DLBCL probably is the most investigated tumor in veterinary medicine, and its relevance as spontaneous model for human DLBCL has been confirmed by these studies. In future, these discoveries will ultimately lead to a better understanding of the underlying disease mechanisms, possibly translating into more effective therapeutic strategies.
弥漫性大 B 细胞淋巴瘤(DLBCL)是世界范围内最常见的犬侵袭性 B 细胞淋巴瘤,新的近期分子方法表明,DLBCL 构成了一种异质性肿瘤,不能仅通过形态学和免疫表型来阐明。DLBCL 表现出侵袭性,通常在短时间内进展,治疗反应可能难以预测。最近,流式细胞术骨髓浸润率已被证明具有预后意义,但需要更敏感的标志物。由于临床行为不同,大量的临床和基础研究致力于确定具有预后或生物学差异的 DLBCL 亚组。通过基因表达谱的转录组分析、通过阵列比较基因组杂交的拷贝数变化和表观遗传改变,勉强描述了这种异质性。使用致癌途径和靶基因的分子亚组也与少数病例的不同结局相关。本文综述的目的是总结犬 DLBCL 的生物学、临床和病理特征的现有知识。迄今为止,DLBCL 可能是兽医研究中最受关注的肿瘤,这些研究证实了其作为人类 DLBCL 自发性模型的相关性。在未来,这些发现最终将有助于更好地了解潜在的疾病机制,并可能转化为更有效的治疗策略。