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急性髓系白血病的新策略:重新定义预后标志物以指导治疗。

New strategies in acute myeloid leukemia: redefining prognostic markers to guide therapy.

机构信息

Division of Hematology/Oncology, Northwestern University-Feinberg School of Medicine, Chicago, IL, USA.

出版信息

Clin Cancer Res. 2012 Oct 1;18(19):5163-71. doi: 10.1158/1078-0432.CCR-12-0313. Epub 2012 Aug 14.

DOI:10.1158/1078-0432.CCR-12-0313
PMID:22893630
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3902112/
Abstract

Although standard therapy for AML has been relatively constant over the past 2 decades, this may be changing with enhanced technologies allowing for the classification of acute myeloid leukemia (AML) into molecularly distinct subsets. Some specific subsets of AML have an excellent prognosis in response to standard therapy, whereas the poor prognosis of AML associated with specific sets of mutations or chromosomal anomalies requires the development of new therapies. Elucidation of the molecular pathogenesis of AML has led to the development of therapies that affect signaling, apoptosis, protein and intermediate metabolism, the surface of the leukemia cell, leukemia cell/stromal interaction, and epigenetic regulation of gene expression.

摘要

尽管过去 20 年来 AML 的标准治疗相对稳定,但随着增强技术的出现,这种情况可能正在发生变化,这些技术可以将急性髓细胞白血病 (AML) 分为分子上明显不同的亚群。某些 AML 亚群对标准治疗有很好的反应,而与特定突变或染色体异常相关的 AML 的不良预后需要开发新的治疗方法。阐明 AML 的分子发病机制导致了靶向信号转导、细胞凋亡、蛋白质和中间代谢、白血病细胞表面、白血病细胞/基质相互作用以及基因表达的表观遗传调控等多个治疗方法的发展。

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