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Protoporphyrin IX is a dual inhibitor of p53/MDM2 and p53/MDM4 interactions and induces apoptosis in B-cell chronic lymphocytic leukemia cells
被引:23
|作者:
Jiang, Liren
[1
,2
,3
]
Malik, Natasha
[1
]
Acedo, Pilar
[1
]
Zawacka-Pankau, Joanna
[1
]
机构:
[1] Karolinska Inst, Dept Microbiol Tumor & Cell Biol, Solnavagen 9, S-17165 Stockholm, Sweden
[2] Uppsala Univ, Med Fac, Dept Immunol Genet & Pathol, Box 25675105, Uppsala, Sweden
[3] Shanghai Jiao Tong Univ, Shanghai Gen Hosp, Dept Pathol Ctr, Sch Med, 100 Haining Rd, Shanghai 200080, Peoples R China
关键词:
CANCER-CELLS;
MUTANT P53;
TRANSCRIPTION FACTOR;
WILD-TYPE;
AMG;
232;
MDM2;
PROTEIN;
CHEMOTHERAPY;
REACTIVATION;
ACTIVATION;
D O I:
10.1038/s41420-019-0157-7
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
p53 is a tumor suppressor, which belongs to the p53 family of proteins. The family consists of p53, p63 and p73 proteins, which share similar structure and function. Activation of wild-type p53 or TAp73 in tumors leads to tumor regression, and small molecules restoring the p53 pathway are in clinical development. Protoporphyrin IX (PpIX), a metabolite of aminolevulinic acid, is a clinically approved drug applied in photodynamic diagnosis and therapy. PpIX induces p53-dependent and TAp73-dependent apoptosis and inhibits TAp73/MDM2 and TAp73/MDM4 interactions. Here we demonstrate that PpIX is a dual inhibitor of p53/MDM2 and p53/MDM4 interactions and activates apoptosis in B-cell chronic lymphocytic leukemia cells without illumination and without affecting normal cells. PpIX stabilizes p53 and TAp73 proteins, induces p53-downstream apoptotic targets and provokes cancer cell death at doses non-toxic to normal cells. Our findings open up new opportunities for repurposing PpIX for treating lymphoblastic leukemia with wild-type TP53.
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页数:11
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