4.7 Article

Chemical constituents from basidiomycete Basidioradulum radula culture medium and their cytotoxic effect on human prostate cancer DU-145 cells

Journal

BIOORGANIC CHEMISTRY
Volume 114, Issue -, Pages -

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bioorg.2021.105064

Keywords

Basidiomycete; Basidioradulum radula; Hyphodermin; DU-145 prostate cancer cell; Cytotoxicity

Funding

  1. Korea University
  2. National Research Foundation of Korea [NRF-2019R1A2C1006226, NRF-2019R1A4A1020626]
  3. Korea Polar Research Institute [PE21150]
  4. Korea Polar Research Institute of Marine Research Placement (KOPRI) [PE21150] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Eight new naphtho [1,2-c]furan derivatives and six known analogues were isolated from the culture medium of Basidioradulum radula, with their structures identified through spectroscopic analysis and absolute configurations resolved using various methods. Compounds 7 and 14 exhibited anti-cancer activity against human prostate cancer cells, but had no effect on the proliferation of splenocytes from immunosuppressed mice.
Eight new naphtho [1,2-c]furan derivatives (1-8) along with six known analogues (9-14) were isolated from culture medium of the basidiomycete Basidioradulum radula. The structures of these compounds were identified using spectroscopic analysis, and their absolute configurations were resolved using X ray diffraction, ECD, and VCD. Compounds 7 and 14 inhibited the cell viability of human prostate cancer DU 145 cells with IC50 values of 7.54 +/- 0.03 mu M and 5.04 +/- 0.03 mu M, respectively. At 8 mu M, compounds 7 and 14 increased the percentage of apoptotic cells and upregulated the protein expression related to the apoptosis caspase pathways in DU 145 cells. Furthermore, the hallmarks of cells undergoing apoptosis, such as chromatin condensation, were also observed at this concentration. However, compound 7 and 14 showed no effect on the proliferation of splenocytes isolated from cyclophosphamide-induce immunosuppressed mice.

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