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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:
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.
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页码:539 / 546
页数:8
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