Decanoic Acid Exerts Its Anti-Tumor Effects via Targeting c-Met Signaling Cascades in Hepatocellular Carcinoma Model

Author:

Yang Min Hee1,Lee Mina2,Deivasigamani Amudha3,Le Duc Dat2,Mohan Chakrabhavi Dhananjaya4,Hui Kam Man3ORCID,Sethi Gautam5,Ahn Kwang Seok1ORCID

Affiliation:

1. Department of Science in Korean Medicine, Kyung Hee University, Seoul 02447, Republic of Korea

2. College of Pharmacy, Sunchon National University, 255 Jungangno, Suncheon-si 57922, Republic of Korea

3. Division of Cellular and Molecular Research, Humphrey Oei Institute of Cancer Research, National Cancer Centre Singapore, Singapore 169610, Singapore

4. FEST Division, CSIR-Indian Institute of Toxicology Research, Vishvigyan Bhawan, 31, Mahatma Gandhi Marg, Lucknow 226001, Uttar Pradesh, India

5. Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117600, Singapore

Abstract

DA, one of the medium-chain fatty acids found in coconut oil, is suggested to have diverse biochemical functions. However, its possible role as a chemoprevention agent in HCC has not been deciphered. Aberrant activation of c-Met can modulate tumor growth and progression in HCC. Here, we report that DA exhibited pro-found anti-tumor effects on human HCC through the suppression of HGF/c-Met signaling cascades in vitro and in vivo. It was noted that DA inhibited HGF-induced activation of c-Met and its downstream signals. DA induced apoptotic cell death and inhibited the expression of diverse tumorigenic proteins. In addition, DA attenuated tumor growth and lung metastasis in the HCC mouse model. Similar to in vitro studies, DA also suppressed the expression of c-Met and its downstream signals in mice tissues. These results highlight the substantial potential of DA in the prevention and treatment of HCC.

Funder

National Research Foundation of Korea

Ministry of Education Tier

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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