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

Authors
Lee, DahaeLee, HeesuKang, Ki SungLee, Jae Wook
Issue Date
May-2018
Publisher
WILEY-V C H VERLAG GMBH
Keywords
Chalcone; Cisplatin; Kidney cells; Renoprotection; MAPK pathway
Citation
BULLETIN OF THE KOREAN CHEMICAL SOCIETY, v.39, no.5, pp.699 - 702
Journal Title
BULLETIN OF THE KOREAN CHEMICAL SOCIETY
Volume
39
Number
5
Start Page
699
End Page
702
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/3789
DOI
10.1002/bkcs.11454
ISSN
1229-5949
Abstract
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.
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College of Korean Medicine (Premedical course of Oriental Medicine)
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