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A versatile drug delivery system targeting senescent cells
被引:217
|作者:
Munoz-Espin, Daniel
[1
,2
]
Rovira, Miguel
[1
,3
]
Galiana, Irene
[4
,5
]
Gimenez, Cristina
[4
]
Lozano-Torres, Beatriz
[4
,5
]
Paez-Ribes, Marta
[2
]
Llanos, Susana
[1
]
Chaib, Selim
[1
,3
]
Munoz-Martin, Maribel
[1
,3
]
Ucero, Alvaro C.
[6
]
Garaulet, Guillermo
[7
]
Mulero, Francisca
[7
]
Dann, Stephen G.
[8
]
VanArsdale, Todd
[8
]
Shields, David J.
[8
]
Bernardos, Andrea
[4
,5
]
Murguia, Jose Ramon
[4
,5
]
Martinez-Manez, Ramon
[4
,5
,9
]
Serrano, Manuel
[1
,3
,10
]
机构:
[1] Spanish Natl Canc Res Ctr CNIO, Tumor Suppress Grp, Madrid, Spain
[2] Univ Cambridge, CRUK Cambridge Ctr, Early Detect Programme, Dept Oncol,Hutchison MRC Res Ctr, Cambridge, England
[3] Barcelona Inst Sci & Technol BIST, Cellular Plast & Dis Grp, Inst Res Biomed IRB Barcelona, Barcelona, Spain
[4] Univ Valencia, Inst Interuniv Invest Reconocimiento Mol & Desarr, Univ Politecn Valencia, Valencia, Spain
[5] CIBER BBN, Madrid, Spain
[6] Spanish Natl Canc Res Ctr CNIO, Genes Dev & Dis Grp, Madrid, Spain
[7] Spanish Natl Canc Res Ctr CNIO, Mol Imaging Unit, Madrid, Spain
[8] Pfizer Inc, Oncol R&D Grp, Pfizer Worldwide Res & Dev, La Jolla, CA USA
[9] Univ Politecn Valencia, Dept Quim, Valencia, Spain
[10] Catalan Inst Res & Adv Studies ICREA, Barcelona, Spain
基金:
欧洲研究理事会;
关键词:
chemotherapy;
fibrosis;
nanomedicine;
palbociclib;
senescence;
MESOPOROUS SILICA NANOPARTICLES;
CELLULAR SENESCENCE;
SECRETORY PHENOTYPE;
BETA-GALACTOSIDASE;
OXIDATIVE STRESS;
DOXORUBICIN;
INHIBITION;
APOPTOSIS;
GENE;
CONTRIBUTES;
D O I:
10.15252/emmm.201809355
中图分类号:
R-3 [医学研究方法];
R3 [基础医学];
学科分类号:
1001 ;
摘要:
Senescent cells accumulate in multiple aging-associated diseases, and eliminating these cells has recently emerged as a promising therapeutic approach. Here, we take advantage of the high lysosomal beta-galactosidase activity of senescent cells to design a drug delivery system based on the encapsulation of drugs with galacto-oligosaccharides. We show that gal-encapsulated fluorophores are preferentially released within senescent cells in mice. In a model of chemotherapy-induced senescence, gal-encapsulated cytotoxic drugs target senescent tumor cells and improve tumor xenograft regression in combination with palbociclib. Moreover, in a model of pulmonary fibrosis in mice, gal-encapsulated cytotoxics target senescent cells, reducing collagen deposition and restoring pulmonary function. Finally, gal-encapsulation reduces the toxic side effects of the cytotoxic drugs. Drug delivery into senescent cells opens new diagnostic and therapeutic applications for senescence-associated disorders.
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页数:18
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