2-Bromo-4,5-Dimethoxy Chalcone Inhibits Cisplatin-induced LLC-PK1 Kidney Cell Death

被引:2
作者
Lee, Dahae [2 ]
Lee, Heesu [3 ]
Kang, Ki Sung [1 ]
Lee, Jae Wook [4 ,5 ,6 ]
机构
[1] Gachon Univ, Coll Korean Med, Seongnam 13120, South Korea
[2] Sungkyunkwan Univ, Sch Pharm, Suwon 16419, South Korea
[3] Gangneung Wonju Natl Univ, Coll Dentisty, Kangnung 25457, South Korea
[4] Korea Inst Sci & Technol, Nat Constituent Res Ctr, Kangnung 25451, South Korea
[5] Korea Inst Sci & Technol, Convergence Res Ctr Dementia, Seoul 02792, South Korea
[6] Korea Univ Sci & Technol, Dept Biol Chem, Daejun 34113, South Korea
基金
新加坡国家研究基金会;
关键词
Chalcone; Cisplatin; Kidney cells; Renoprotection; MAPK pathway; BIOLOGICAL EVALUATION; INDUCED CYTOTOXICITY; TYROSINE KINASE; AGENTS; ANALOGS; APOPTOSIS; INJURY; ISOLIQUIRITIGENIN; PATHWAYS; DESIGN;
D O I
10.1002/bkcs.11454
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The kidney has various functions, including modulating blood pressure, balancing electrolytes, and controlling blood volume. Among these functions, extracting metabolic waste from blood plays an important role in kidney. 1,2 Additionally, kidney epithelial cells are vulnerable to the toxic effects of various chemical agents and medications. 3,4 Recently, cisplatin, an inorganic platinum-based chemotherapeutic agent, has been used to inhibit solid malignant tumors due to its high therapeutic potential. 5,6 However, continuous exposure to cisplatin can cause various significant side effects, such as bone marrow suppression, peripheral neuropathy, and nephrotoxicity. In particular, a single dose of cisplatin treatment can cause nephrotoxicity among one-third of patients.(7-9) Therefore, it has been suggested to develop medication for cisplatin-induced nephrotoxicity.
引用
收藏
页码:699 / 702
页数:4
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