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T细胞白血病和淋巴瘤的分子发病机制

Molecular pathogenesis of T-cell leukaemia and lymphoma.

作者信息

Aifantis Iannis, Raetz Elizabeth, Buonamici Silvia

机构信息

Department of Pathology, New York University School of Medicine, 550 First Avenue, New York, New York 10016, USA.

出版信息

Nat Rev Immunol. 2008 May;8(5):380-90. doi: 10.1038/nri2304.

Abstract

T-cell acute lymphoblastic leukaemia (T-ALL) is induced by the transformation of T-cell progenitors and mainly occurs in children and adolescents. Although treatment outcome in patients with T-ALL has improved in recent years, patients with relapsed disease continue to have a poor prognosis. It is therefore important to understand the molecular pathways that control both the induction of transformation and the treatment of relapsed disease. In this Review, we focus on the molecular mechanisms responsible for disease induction and maintenance. We also compare the physiological progression of T-cell differentiation with T-cell transformation, highlighting the close relationship between these two processes. Finally, we discuss potential new therapies that target oncogenic pathways in T-ALL.

摘要

T细胞急性淋巴细胞白血病(T-ALL)由T细胞祖细胞转化引起,主要发生于儿童和青少年。尽管近年来T-ALL患者的治疗效果有所改善,但复发患者的预后仍然很差。因此,了解控制转化诱导和复发疾病治疗的分子途径很重要。在本综述中,我们重点关注负责疾病诱导和维持的分子机制。我们还比较了T细胞分化与T细胞转化的生理进程,强调了这两个过程之间的密切关系。最后,我们讨论了针对T-ALL致癌途径的潜在新疗法。

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