Therapeutic targeting of IL-7Rα signaling pathways in ALL treatment

被引：34

作者：

Cramer, Sarah D. ^{[1
,2
,3
]}

Aplan, Peter D. ^{[4
]}

Durum, Scott K. ^{[1
]}

机构：

[1] NCI, Cytokines & Immun Sect, Canc & Inflammat Program, NIH, Bldg 560,Room 31-71, Frederick, MD 21702 USA

[2] NIH, Comparat Biomed Scientist Training Program, Bldg 10, Bethesda, MD 20892 USA

[3] Univ Maryland, Dept Vet Med, College Pk, MD 20742 USA

[4] NCI, Leukemia Biol Sect, Genet Branch, NIH, Bethesda, MD 20892 USA

来源：

BLOOD | 2016年 / 128卷 / 04期

基金：

美国国家卫生研究院;

关键词：

ACUTE LYMPHOBLASTIC-LEUKEMIA; B-CELL PRECURSOR; CHILDRENS ONCOLOGY GROUP; THYMIC STROMAL LYMPHOPOIETIN; MURINE XENOGRAFT MODELS; OF-FUNCTION MUTATIONS; T-ALL; CYTOTOXIC ACTIVITY; CRLF2; EXPRESSION; MTOR INHIBITORS;

D O I：

10.1182/blood-2016-03-679209

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Increased understanding of pediatric acute lymphoblastic leukemia (ALL) pathobiology has led to dramatic improvements in patient survival. However, there is still a needto developtargeted therapies toenable reduced chemotherapy intensity and to treat relapsed patients. The interleukin-7 receptor alpha ( IL-7R alpha) signaling pathways areprime therapeutic targetsbecause these pathways harbor genetic aberrations in both T-cell ALL and B-cell precursor ALL. Therapeutic targeting of the IL-7R alpha signaling pathways may lead to improved outcomes in a subset of patients.

引用

页码：473 / 478

页数：6

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