Absolute Stereochemistry and Cytotoxic Effects of Vismione E from Marine Sponge-Derived Fungus Aspergillus sp. 1901NT-1.2.2

Author:

Girich Elena V.1ORCID,Trinh Phan Thi Hoai2ORCID,Nesterenko Liliana E.13,Popov Roman S.1ORCID,Kim Natalya Yu.1,Rasin Anton B.1,Menchinskaya Ekaterina S.1,Kuzmich Aleksandra S.1,Chingizova Ekaterina A.1,Minin Artem S.45ORCID,Ngoc Ngo Thi Duy2,Van Tran Thi Thanh2,Yurchenko Ekaterina A.1ORCID,Yurchenko Anton N.1ORCID,Berdyshev Dmitry V.1

Affiliation:

1. G.B. Elyakov Pacific Institute of Bioorganic Chemistry, Far Eastern Branch of the Russian Academy of Sciences, Prospect 100-Letiya Vladivostoka, 159, Vladivostok 690022, Russia

2. Department of Marine Biotechnology, Nhatrang Institute of Technology Research and Application, Vietnam Academy of Science and Technology, Nha Trang 650000, Vietnam

3. Institute of High Technologies and Advanced Materials, Far Eastern Federal University, 10 Ajax Bay, Russky Island, Vladivostok 690922, Russia

4. M.N. Mikheev Institute of Metal Physics of the Ural Branch of the Russian Academy of Sciences, S. Kovalevskoi, 18, Ekaterinburg 620108, Russia

5. Institute of Natural Sciences and Mathematics, The Ural Federal University Named after the First President of Russia B. N. Yeltsin, Lenina Av., 51, Ekaterinburg 620083, Russia

Abstract

The metabolic profile of the Aspergillus sp. 1901NT-1.2.2 sponge-associated fungal strain was investigated using the HPLC MS technique, and more than 23 peaks in the HPLC MS chromatogram were detected. Only two minor peaks were identified as endocrocin and terpene derivative MS data from the GNPS database. The main compound was isolated and identified as known anthraquinone derivative vismione E. The absolute stereochemistry of vismione E was established for the first time using ECD and quantum chemical methods. Vismione E showed high cytotoxic activity against human breast cancer MCF-7 cells, with an IC50 of 9.0 µM, in comparison with low toxicity for normal human breast MCF-10A cells, with an IC50 of 65.3 µM. It was found that vismione E inhibits MCF-7 cell proliferation and arrests the cell cycle in the G1 phase. Moreover, the negative influence of vismione E on MCF-7 cell migration was detected. Molecular docking of vismione E suggested the IMPDH2 enzyme as one of the molecular targets for this anthraquinone derivative.

Funder

Russian Foundation for Basic Research

Vietnam Academy of Science and Technology

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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