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Glycosidase-activated H2S donorsto enhance chemotherapy efficacy
被引:0
|作者:
Ye, Zizhen
[1
]
Li, Jixiang
[1
]
Shi, Jiarui
[1
]
Song, Yuguang
[1
]
Liu, Yangping
[1
]
Hou, Jingli
[1
]
机构:
[1] Tianjin Med Univ, Sch Pharm, Tianjin Key Lab Technol Enabling Dev Clin Therape, Tianjin 300070, Peoples R China
关键词:
HYDROGEN-SULFIDE;
IN-VITRO;
CANCER;
FAMILY;
D O I:
10.1016/j.bmcl.2024.129644
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
Hydrogen sulfide (H2S) plays a critical role in cancer biology. Herein, we developed a series of glycosidase-triggered hydrogen sulfide (H2S) donors by connecting sugar moieties (including glucose, galactose and mannose) to COS donors via a self-immolative spacer. In the presence of corresponding glycosidases, H2S was gradually released from these donors in PBS buffer with releasing efficiencies from 36 to 67 %. H2S release was also detected by H2S probe WSP-1 after treatment HepG2 cells with Man1. Cytotoxicities of these glycosylated H2S donors were evaluated against HepG2 by MTT assay. Among them, Man1 and Man2 exhibited an obvious reduction of cell viability in HepG2 cells, with cell viability as 37.6 % for 80 mu M of Man. Consistently, significant apoptosis was observed in HepG2 cells after treatment with Man1 and Man2. Finally, We evaluated the potential of Man1 for combination therapy with doxorubicin. A synergistic effect was observed between Man1 and Doxorubicin in HepG2 and Hela cells. All these results indicated glycosidase-activated H2S donorshave promising potential for cancer therapy.
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