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滤泡性淋巴瘤的转化途径。

The routes for transformation of follicular lymphoma.

作者信息

Okosun Jessica, Montoto Silvia, Fitzgibbon Jude

机构信息

aCentre for Haemato-Oncology, Barts Cancer Institute bDepartment of Haemato-oncology, St Bartholomew's Hospital, Barts Health NHS Trust, London, UK.

出版信息

Curr Opin Hematol. 2016 Jul;23(4):385-91. doi: 10.1097/MOH.0000000000000255.

Abstract

PURPOSE OF REVIEW

Aggressive transformation, a frequent event in the natural history of follicular lymphoma, is associated with increased lymphoma-related mortality and yet the underlying biology remains poorly defined. This review outlines recent advances in our understanding of the genetic basis and evolutionary process leading to transformation.

RECENT FINDINGS

Both the antecedent indolent and transformed follicular lymphoma (tFL) arise through branched divergent evolution with tumors emerging from a founder precursor population, the common progenitor cell. Although the majority of tFLs maintain a germinal center B-cell gene expression signature, an activated B-cell-type (ABC-type) profile appears to predominate in BCL2-translocation negative cases. It does not appear that a single unifying genetic or epigenetic event promotes a fitter and more aggressive clone.

SUMMARY

Transformed follicular tumors are genetically heterogeneous perhaps reflecting the varying clinical behavior and outcomes of this disease event. Follicular lymphoma and tFL remain incurable tumors highlighted by our inability to eradicate the founder common progenitor cell population with current therapies. Progress has now been made in defining the genetic events and evolutionary pathways responsible for transformation. Although more research is required in predicting and understanding the biology of transformation, there are opportunities to improve outcomes by preferentially directing targeted therapies toward 'actionable' early and transformation-specific aberrations.

摘要

综述目的

侵袭性转化是滤泡性淋巴瘤自然病程中常见的事件,与淋巴瘤相关死亡率增加有关,但其潜在生物学机制仍不清楚。本综述概述了我们对导致转化的遗传基础和进化过程理解的最新进展。

最新发现

惰性滤泡性淋巴瘤及其转化型(tFL)均通过分支发散进化产生,肿瘤起源于一个始祖前体细胞群,即共同祖细胞。虽然大多数tFL维持生发中心B细胞基因表达特征,但在BCL2易位阴性病例中,活化B细胞型(ABC型)特征似乎占主导。似乎没有单一的统一遗传或表观遗传事件能促进更适应且更具侵袭性的克隆。

总结

转化型滤泡性肿瘤在基因上具有异质性,这可能反映了该疾病事件不同的临床行为和结局。滤泡性淋巴瘤和tFL仍然是无法治愈的肿瘤,这突出表现在我们目前的治疗无法根除始祖共同祖细胞群。目前在确定导致转化的遗传事件和进化途径方面已取得进展。虽然在预测和理解转化生物学方面还需要更多研究,但有机会通过优先将靶向治疗导向“可操作的”早期和转化特异性畸变来改善预后。

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