Marinobazzanan, a Bazzanane-Type Sesquiterpenoid, Suppresses the Cell Motility and Tumorigenesis in Cancer Cells

Author:

Pulat Sultan1ORCID,Hillman Prima F.2,Kim Sojeong3,Asolkar Ratnakar N.4ORCID,Kim Haerin3,Zhou Rui1,Taş İsa1ORCID,Gamage Chathurika D. B.1ORCID,Varlı Mücahit1ORCID,Park So-Yeon1ORCID,Park Sung Chul5,Yang Inho6ORCID,Shin Jongheon5ORCID,Oh Dong-Chan5,Kim Hangun1ORCID,Nam Sang-Jip2,Fenical William4

Affiliation:

1. College of Pharmacy and Research Institute of Life and Pharmaceutical Sciences, Sunchon National University, Sunchon 57922, Republic of Korea

2. Department of Chemistry and Nanoscience, Ewha Womans University, Seoul 03760, Republic of Korea

3. Graduate School of Industrial Pharmaceutical Sciences, Ewha Womans University, Seoul 03760, Republic of Korea

4. Center for Marine Biotechnology and Biomedicine, Scripps Institution of Oceanography, University of California-San Diego, La Jolla, CA 92093-0204, USA

5. Natural Products Research Institute, College of Pharmacy, Seoul National University, San 56-1, Sillim, Gwanak, Seoul 08826, Republic of Korea

6. Department of Convergence Study on the Ocean Science and Technology, Korea Maritime and Ocean University, Busan 49112, Republic of Korea

Abstract

Marinobazzanan (1), a new bazzanane-type sesquiterpenoid, was isolated from a marine-derived fungus belonging to the genus Acremonium. The chemical structure of 1 was elucidated using NMR and mass spectroscopic data, while the relative configurations were established through the analysis of NOESY data. The absolute configurations of 1 were determined by the modified Mosher’s method as well as vibrational circular dichroism (VCD) spectra calculation and it was determined as 6R, 7R, 9R, and 10R. It was found that compound 1 was not cytotoxic to human cancer cells, including A549 (lung cancer), AGS (gastric cancer), and Caco-2 (colorectal cancer) below the concentration of 25 μM. However, compound 1 was shown to significantly decrease cancer-cell migration and invasion and soft-agar colony-formation ability at concentrations ranging from 1 to 5 μM by downregulating the expression level of KITENIN and upregulating the expression level of KAI1. Compound 1 suppressed β-catenin-mediated TOPFLASH activity and its downstream targets in AGS, A549, and Caco-2 and slightly suppressed the Notch signal pathway in three cancer cells. Furthermore, 1 also reduced the number of metastatic nodules in an intraperitoneal xenograft mouse model.

Funder

National Research Foundation of Korea

US NIH National Cancer Institute

Publisher

MDPI AG

Subject

Drug Discovery,Pharmacology, Toxicology and Pharmaceutics (miscellaneous),Pharmaceutical Science

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