Methanol Extract of Petasites japonicas Promotes Apoptosis via the MAPK and ROS-dependent Signaling Pathways

Author:

Choi Na-Ri1,Choi Woo-Gyun1,Kwon Min Ji1,Park Joon23,Kim Yun Tai23,Lee Min Jae4,Park Jae-Woo56,Woo Joo Han7,Kim Byung Joo1ORCID

Affiliation:

1. Department of Longevity and Biofunctional Medicine, Pusan National University School of Korean Medicine, Yangsan, Republic of Korea

2. Division of Food Functionality, Korea Food Research Institute, Wanju-gun, Republic of Korea

3. Department of Food Biotechnology, Korea University of Science & Technology, Daejeon, Republic of Korea

4. Department of Veterinary Medicine, College of Veterinary Medicine, Kangwon National University, Chuncheon, Republic of Korea

5. Department of Gastroenterology, College of Korean Medicine, Kyung Hee University, Seoul, Republic of Korea

6. Department of Clinical Korean Medicine, Graduate School of Kyung Hee University, Seoul, Republic of Korea

7. Department of Physiology, Dongguk University College of Medicine, Gyeongju, Republic of Korea

Abstract

Background: Petasites japonicus (PJ), also known as Butterbur, has a rich history as a traditional healing remedy across numerous countries. Objectives: This study was designed to evaluate the potential anti-cancer properties of the methanol extract derived from PJ (PJE). Materials and Methods: Cell viability was measured with 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide. Cell cycle analysis, caspase activity assays, western blotting, and reactive oxygen species (ROS) assays were also used to investigate the anticancer effects of PJE on cancer cells. Results: It was shown that PJE inhibited the cell viability of the colon carcinoma cell line Caco-2 (half-maximal inhibitory concentration [IC50]: 268.4 µg/mL), of the hepatocellular carcinoma cell line Hep3B (IC50: 420.2 µg/mL), and of the bladder carcinoma cell line 5637 (IC50: 99.43 µg/mL). Analysis of DNA content indicated an increase in the sub-G1 population of 5637 cells as a result of PJE treatment. Furthermore, PJE caused a reduction in mitochondrial membrane potential and the ratio of Bcl-2 to Bax. Moreover, PJE enhanced the levels of various components involved in the proapoptotic cascade, such as caspase-3, caspase-9, and poly-adenosine diphosphate-ribose polymerase. Moreover, it was observed that PJE modulated mitogen-activated protein kinases (MAPKs) activation and induced an elevation in intracellular production of ROS. Conclusion: These combined results strongly suggest that PJE possesses significant proapoptotic properties as an herbal medicine, acting through ROS-dependent MAPK signaling pathways in bladder cancer cells.

Publisher

SAGE Publications

Subject

Drug Discovery,Pharmaceutical Science

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