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Novel Caffeic Acid Phenethyl Ester-Mortalin Antibody Nanoparticles Offer Enhanced Selective Cytotoxicity to Cancer Cells
被引:18
|作者:
Wang, Jia
[1
,2
]
Bhargava, Priyanshu
[1
]
Yu, Yue
[1
,3
]
Sari, Anissa Nofita
[1
]
Zhang, Huayue
[1
]
Ishii, Noriyuki
[1
]
Yan, Kangmin
[1
]
Zhang, Zhenya
[2
]
Ishida, Yoshiyuki
[4
]
Terao, Keiji
[4
]
Kaul, Sunil C.
[1
,5
]
Miyako, Eijiro
[6
]
Wadhwa, Renu
[1
]
机构:
[1] Natl Inst Adv Ind Sci & Technol, DBT AIST Int Ctr Translat & Environm Res DAICENTE, AIST INDIA DAILAB, Tsukuba, Ibaraki 3058565, Japan
[2] Univ Tsukuba, Grad Sch Life & Environm Sci, Tsukuba, Ibaraki 3058575, Japan
[3] Natl Inst Adv Ind Sci & Technol, Biomed Res Inst BMRI, Ikeda, Osaka 5638577, Japan
[4] CycloChem Co Ltd, Chuo Ku, 7-4-5 Minatojima Minamimachi, Kobe, Hyogo 6500047, Japan
[5] KAUL Tech Co Ltd, 3-24 Nagakunidai, Tsuchiura, Ibaraki 3000810, Japan
[6] Japan Adv Inst Sci & Technol, Sch Mat Sci, 1-1 Asahidai, Nomi, Ishikawa 9231292, Japan
来源:
关键词:
CAPE;
mortalin;
internalizing antibody;
nanoparticles;
enhanced drug delivery;
cancer therapy;
BRAZILIAN GREEN PROPOLIS;
ANTICANCER ACTIVITY;
ANTIVIRAL ACTIVITY;
CARF COLLABORATOR;
APOPTOSIS;
INHIBITION;
CAPE;
DELIVERY;
GROWTH;
SUPPRESSES;
D O I:
10.3390/cancers12092370
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Caffeic acid phenethyl ester (CAPE) is a key bioactive ingredient of honeybee propolis and is claimed to have anticancer activity. Since mortalin, a hsp70 chaperone, is enriched in a cancerous cell surface, we recruited a unique cell internalizing anti-mortalin antibody (MotAb) to generate mortalin-targeting CAPE nanoparticles (CAPE-MotAb). Biophysical and biomolecular analyses revealed enhanced anticancer activity of CAPE-MotAb both in in vitro and in vivo assays. We demonstrate that CAPE-MotAb cause a stronger dose-dependent growth arrest/apoptosis of cancer cells through the downregulation of Cyclin D1-CDK4, phospho-Rb, PARP-1, and anti-apoptotic protein Bcl2. Concomitantly, a significant increase in the expression of p53, p21(WAF1), and caspase cleavage was obtained only in CAPE-MotAb treated cells. We also demonstrate that CAPE-MotAb caused a remarkably enhanced downregulation of proteins critically involved in cell migration. In vivo tumor growth assays for subcutaneous xenografts in nude mice also revealed a significantly enhanced suppression of tumor growth in the treated group suggesting that these novel CAPE-MotAb nanoparticles may serve as a potent anticancer nanomedicine.
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页码:1 / 21
页数:21
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