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
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.
引用
收藏
页码:1 / 21
页数:21
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