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SP-8356, a (15)-(-)-Verbenone Derivative, Inhibits the Growth and Motility of Liver Cancer Cells by Regulating NF-kappa B and ERK Signaling

Authors
Kim, Dong HwiYong, Hyo JeongMander, SunamHuong Thi NguyenLan Phuong NguyenPark, Hee-KyungCha, Hyo KyeongKim, Won-KiHwang, Jong-Ik
Issue Date
5월-2021
Publisher
KOREAN SOC APPLIED PHARMACOLOGY
Keywords
SP-8356; Liver cancer; Proliferation; Motility; ERK; NF-kappa B
Citation
BIOMOLECULES & THERAPEUTICS, v.29, no.2, pp.331 - 341
Indexed
SCIE
SCOPUS
KCI
Journal Title
BIOMOLECULES & THERAPEUTICS
Volume
29
Number
2
Start Page
331
End Page
341
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/128123
DOI
10.4062/biomolther.2020.200
ISSN
1976-9148
Abstract
Liver cancer is a common tumor and currently the second leading cause of cancer-related mortality globally. Liver cancer is highly related to inflammation as more than 90% of liver cancer arises in the context of hepatic inflammation, such as hepatitis B virus and hepatitis C virus infection. Despite significant improvements in the therapeutic modalities for liver cancer, patient prognosis is not satisfactory due to the limited efficacy of current drug therapies in anti-metastatic activity. Therefore, developing new effective anti-cancer agents with anti-metastatic activity is important for the treatment of liver cancer. In this study, SP-8356, a verbenone derivative with anti-inflammatory activity, was investigated for its effect on the growth and migration of liver cancer cells. Our findings demonstrated that SP-8356 inhibits the proliferation of liver cancer cells by inducing apoptosis and suppressing the mobility and invasion ability of liver cancer cells. Functional studies revealed that SP-8356 inhibits the mitogen-activated protein kinase and nuclear factor-kappa B signaling pathways, which are related to cell proliferation and metastasis, resulting in the downregulation of metastasis-related genes. Moreover, using an orthotopic liver cancer model, tumor growth was significantly decreased following treatment with SP-8356. Thus, this study suggests that SP-8356 may be a potential agent for the treatment of liver cancer with multimodal regulation.
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