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Genipin increases oxaliplatin-induced cell death through autophagy in gastric cancer

Authors
Kim, Bo RamJeong, Yoon A.Kim, Dae YoungKim, Jung LimJeong, SoyeonNa, Yoo JinYun, Hye KyeongPark, Seong HyeJo, Min LeeAshktorab, HassanSmoot, Duane T.Lee, Dae-HeeOh, Sang Cheul
Issue Date
2020
Publisher
IVYSPRING INT PUBL
Keywords
Autophagy; Genipin; Oxaliplatin; p53
Citation
JOURNAL OF CANCER, v.11, no.2, pp.460 - 467
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF CANCER
Volume
11
Number
2
Start Page
460
End Page
467
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/139109
DOI
10.7150/jca.34773
ISSN
1837-9664
Abstract
Oxaliplatin is used for treatment in combination with many drugs. However, the survival rate is still low due to side effects and drug resistance. Therefore, the combination with natural products was required for increasing efficacy and reducing side effects. Genipin, a natural product derived from the Gardenia jasminoides, associated with anti-angiogenic, anti-proliferative, hypertension, inflammatory, and the Hedgehog pathway. It is not known that genipin increases the therapeutic effect of oxaliplatin in gastric cancer. In this study, we found that genipin sensitizes oxaliplatin-induced apoptosis for the first time using colony forming assay, FACS analysis, and western blotting in gastric cancer. Additionally, genipin induced p53 expression in AGS, MKN45, and MKN28 cells. Also, genipin induced autophagy and LC3 expression. Knockdown of LC3 decreased cell death enhanced by the combination of oxaliplatin and genipin. In summary, we showed that genipin increases the oxaliplatin-induced cell death via p53-DRAM autophagy. Based on this, we suggest that genipin is a sensitizer of oxaliplatin.
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