Cell Penetrating Peptides as a Therapeutic Strategy in Chronic Lymphocytic Leukemia

被引:9
|
作者
Arrouss, Issam [1 ]
Decaudin, Didier [2 ,3 ]
Choquet, Sylvain [4 ]
Azar, Nabih [4 ]
Parizot, Christophe [5 ]
Zini, Jean M. [6 ]
Nemati, Fariba [3 ]
Rebollo, Angelita [1 ]
机构
[1] Univ Paris 06, INSERM, UMRS 945, F-75013 Paris, France
[2] Inst Curie, Dept Med Hematol, Paris, France
[3] Inst Curie, Translat Res Dept, Lab Preclin Invest, Paris, France
[4] Hop La Pitie Salpetriere, Serv Hematol Clin, Paris, France
[5] Hop La Pitie Salpetriere, AP HP, Dept Immunol Cellulaire & Tissulaire, Paris, France
[6] Hop St Louis, AP HP, Serv Hematol, Paris, France
来源
PROTEIN AND PEPTIDE LETTERS | 2015年 / 22卷 / 06期
关键词
apoptosis; Caspase-9; CLL; penetrating peptides; PP2A; APOPTOSIS; PROTEINS; SURVIVAL; PATHWAY; TARGET;
D O I
10.2174/0929866522666150216115352
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
PP2A is a serine/threonine phosphatase critical to a number of physiological and developmental processes. In this manuscript, we show that a peptide, specifically blocking the caspase9/PP2A interaction, DPT-C9h, induces apoptosis in primary tumour B cells isolated from peripheral blood mononuclear cells or bone marrow of chronic lymphocytic leukemia (CLL) patients, but not on B cells obtained from healthy donors (HD). Moreover, in both CLL patients and HD, DPT-C9h does not induce apoptosis on T-and NKcells and monocytes. Our results strongly suggest that DPT-C9h peptide has tumour specificity and that caspase-9/PP2Ac interaction constitutes a novel therapeutic approach for the treatment in CLL patients.
引用
收藏
页码:539 / 546
页数:8
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