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为急性淋巴细胞白血病患儿研发更优疗法。

Building better therapy for children with acute lymphoblastic leukemia.

作者信息

Carroll William L, Raetz Elizabeth A

机构信息

Stephen D. Hassenfeld Children's Center for Cancer and Blood Diseases, New York University Cancer Institute, New York, New York 10016, USA.

出版信息

Cancer Cell. 2005 Apr;7(4):289-91. doi: 10.1016/j.ccr.2005.04.003.

Abstract

Childhood acute lymphoblastic leukemia is one of the most curable of all human cancers, but new approaches are urgently needed for children who relapse and to avoid severe side effects of curative therapy. Work from the laboratories of Rob Pieters and William Evans, including a paper in this issue of Cancer Cell, has led to the identification of genes whose expression correlates with drug crossresistance and long term outcome. The goal is now to integrate these and other findings using gene expression technology into the care of children with the most common pediatric malignancy.

摘要

儿童急性淋巴细胞白血病是所有人类癌症中最可治愈的疾病之一,但对于复发的儿童以及避免根治性治疗的严重副作用,迫切需要新的方法。罗布·彼得斯(Rob Pieters)和威廉·埃文斯(William Evans)实验室的研究工作,包括发表在本期《癌细胞》杂志上的一篇论文,已经鉴定出了一些基因,其表达与药物交叉耐药性和长期预后相关。现在的目标是利用基因表达技术将这些以及其他研究结果整合到这种最常见的儿童恶性肿瘤的治疗中。

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