Please use this identifier to cite or link to this item: https://doi.org/10.3390/cancers13061347
Title: A novel role of bergamottin in attenuating cancer associated cachexia by diverse molecular mechanisms
Authors: Jung, Young Yun
Ko, Jeong-Hyeon
Um, Jae-Young
Sethi, Gautam 
Ahn, Kwang Seok
Keywords: Bergamottin
Cachexia
Conditioned media
ERK
STAT3
Issue Date: 17-Mar-2021
Publisher: MDPI AG
Citation: Jung, Young Yun, Ko, Jeong-Hyeon, Um, Jae-Young, Sethi, Gautam, Ahn, Kwang Seok (2021-03-17). A novel role of bergamottin in attenuating cancer associated cachexia by diverse molecular mechanisms. Cancers 13 (6) : 1-16. ScholarBank@NUS Repository. https://doi.org/10.3390/cancers13061347
Rights: Attribution 4.0 International
Abstract: Purpose: The potential effects of bergamotiin (BGM) on the suppression of cancer cachexia was evaluated under in vitro and in vivo conditions to investigate its possible inhibitory effects on the muscle and fat loss. Method: The differentiated C2C12 and 3T3L1 cells were treated with BGM after the induction of cancer-cachexia with pancreatic cancer conditioned media (CM). The expression levels of the various molecules involved in the differentiation and loss of muscle and fat (MuRF-1, Atrogin-1, C/EBP?, and PPAR?) were analyzed by Western blot and oil red O staining. For in vivo experiment, MIA PaCa-2 cells were injected into the mice (n = 6), and then BGM (1 mg/kg) was intraperitoneally administered to analyze muscle and adipose tissue by Hematoxylin and Eosin staining and Western blot. Result: BGM displayed a significant effect on the inhibition of muscle and fat catabolism under both in vitro and in vivo conditions. The results of the in vivo experiment revealed a remarkable suppressive effect of BGM on the weight loss in mice. Conclusions: The potential effects of BGM on the inhibition of muscle and fat catabolism in vitro and in vivo were thus confirmed. Based on the results, the impact of BGM on cancer cachexia could be possibly analyzed in the future clinical studies. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
Source Title: Cancers
URI: https://scholarbank.nus.edu.sg/handle/10635/233223
ISSN: 2072-6694
DOI: 10.3390/cancers13061347
Rights: Attribution 4.0 International
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