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T细胞急性淋巴细胞白血病的病理生理学:聚焦分子层面

The Physiopathology of T- Cell Acute Lymphoblastic Leukemia: Focus on Molecular Aspects.

作者信息

Fattizzo Bruno, Rosa Jessica, Giannotta Juri Alessandro, Baldini Luca, Fracchiolla Nicola Stefano

机构信息

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico di Milano, Milan, Italy.

Dipartimento di Oncologia ed Oncoematologia, Università degli studi di Milano, Milan, Italy.

出版信息

Front Oncol. 2020 Feb 28;10:273. doi: 10.3389/fonc.2020.00273. eCollection 2020.

Abstract

T-cell acute lymphoblastic leukemia/lymphoma is an aggressive hematological neoplasm whose classification is still based on immunophenotypic findings. Frontline treatment encompass high intensity combination chemotherapy with good overall survival; however, relapsing/refractory patients have very limited options. In the last years, the understanding of molecular physiopathology of this disease, lead to the identification of a subset of patients with peculiar genetic profile, namely "early T-cell precursors" lymphoblastic leukemia, characterized by dismal outcome and indication to frontline allogeneic bone marrow transplant. In general, the most common mutations occur in the NOTCH1/FBXW7 pathway (60% of adult patients), with a positive prognostic impact. Other pathogenic steps encompass transcriptional deregulation of oncogenes/oncosuppressors, cell cycle deregulation, kinase signaling (including IL7R-JAK-STAT pathway, PI3K/AKT/mTOR pathway, RAS/MAPK signaling pathway, ABL1 signaling pathway), epigenetic deregulation, ribosomal dysfunction, and altered expression of oncogenic miRNAs or long non-coding RNA. The insight in the genomic landscape of the disease paves the way to the use of novel targeted drugs that might improve the outcome, particularly in relapse/refractory patients. In this review, we analyse available literature on T-ALL pathogenesis, focusing on molecular aspects of clinical, prognostic, and therapeutic significance.

摘要

T 细胞急性淋巴细胞白血病/淋巴瘤是一种侵袭性血液肿瘤,其分类仍基于免疫表型结果。一线治疗包括高强度联合化疗,总体生存率良好;然而,复发/难治性患者的选择非常有限。在过去几年中,对这种疾病分子生理病理学的认识,导致识别出一部分具有特殊基因特征的患者,即“早期 T 细胞前体”淋巴细胞白血病,其特点是预后不良且适合一线异基因骨髓移植。一般来说,最常见的突变发生在 NOTCH1/FBXW7 通路(60%的成年患者),具有积极的预后影响。其他致病步骤包括癌基因/抑癌基因的转录失调、细胞周期失调、激酶信号传导(包括 IL7R-JAK-STAT 通路、PI3K/AKT/mTOR 通路、RAS/MAPK 信号通路、ABL1 信号通路)、表观遗传失调、核糖体功能障碍以及致癌 miRNA 或长链非编码 RNA 的表达改变。对该疾病基因组格局的深入了解为使用可能改善预后的新型靶向药物铺平了道路,特别是在复发/难治性患者中。在这篇综述中,我们分析了关于 T 细胞急性淋巴细胞白血病发病机制的现有文献,重点关注临床、预后和治疗意义的分子方面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4055/7059203/49208844dfa2/fonc-10-00273-g0001.jpg

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