Cytotoxic furanosesquiterpenoids and steroids from Ircinia mutans sponges

Pharm Biol. 2021 Dec;59(1):575-583. doi: 10.1080/13880209.2021.1920620.

Abstract

Context: Ircinia mutans Wilson (Irciniidae) is a sponge with antimicrobial and cytotoxic constituents.

Objective: Our objective was to characterise the cytotoxic constituents of two seasonal collections of I. mutans.

Materials and methods: The sponges were extracted in methanol-dichloromethane and their constituents were purified and characterised using column chromatography, GC-MS, 1 D and 2 D NMR. Anti-proliferative activities of the compounds, were evaluated using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) colorimetric assay (0.25-100 μg/mL, 72 h) against leukaemia (MOLT-4), breast (MCF-7) and colon cancer (HT-29) human cells.

Results: Three furanosesquiterpoids; furodysin (1), ent-furodysinin (2) and furoircin (3) and ten sterols were characterised in I. mutans, for the first time. Cholesterol (4), cholesta-5, 7-dien-3β-ol (5) and ergosterol (6) were determined in the sponge from the winter collections, while cholesta-5, 22-dien-3β-ol (7), 24-methyldesmosterol (8), campesterol (9), stigmasterol (10), γ-ergostenol (11), chondrillasterol (12) and γ-sitosterol (13) were detected in the summer samples. The steroids from the winter collection exhibited cytotoxic activity with IC50 values of 13.0 ± 0.9, 11.1 ± 1.7 and 1.1 ± 0.4 µg/mL, against the mentioned cancer cell lines, respectively, while those from the summer sample, showed greater activity, IC50 = 1.1 ± 0.2 μg/mL against MOLT-4. The purified steroids showed potent MOLT-4 cytotoxic activity, IC50 values = 2.3-7.8 µg/mL.

Discussion and conclusion: The present study suggests that I. mutans is a rich source of cytotoxic steroids, and introduces 3 as new natural product. Considering the high cytotoxic activity of the steroids, these structures could be candidates for anticancer drug development in future research.

Keywords: Furanosesquiterpenes; cholesterol; ergosterol; marine sponge; stigmasterol; γ-sitosterol.

MeSH terms

  • Animals
  • Antineoplastic Agents / administration & dosage
  • Antineoplastic Agents / isolation & purification
  • Antineoplastic Agents / pharmacology*
  • Breast Neoplasms / drug therapy
  • Breast Neoplasms / pathology
  • Cell Line, Tumor
  • Colonic Neoplasms / drug therapy
  • Colonic Neoplasms / pathology
  • Female
  • HT29 Cells
  • Humans
  • Inhibitory Concentration 50
  • Leukemia / drug therapy
  • Leukemia / pathology
  • MCF-7 Cells
  • Porifera / chemistry*
  • Sesquiterpenes / administration & dosage
  • Sesquiterpenes / isolation & purification
  • Sesquiterpenes / pharmacology*
  • Steroids / administration & dosage
  • Steroids / isolation & purification
  • Steroids / pharmacology*

Substances

  • Antineoplastic Agents
  • Sesquiterpenes
  • Steroids

Grants and funding

This research was funded by the University of Hormozgan, Bandar Abbas; the Shiraz University of Medical Sciences; Vice-Provosts for Researches and the Alexander von Humboldt foundation for a research group linkage program grant [3.4 - IRN/1101775].