Evaluation of cancer-preventive activity and structure-activity relationships of 3-demethylubiquinone Q2, isolated from the ascidian Aplidium glabrum, and its synthetic analogs

• Published in: Pharmaceutical research Vol. 23; no. 1; pp. 70 - 81
• Main Authors: FEDOROV, Sergey N, RADCHENKO, Oleg S, SHUBINA, Larisa K, BALANEVA, Nadezhda N, BODE, Ann M, STONIK, Valentin A, ZIGANG DONG
• Format: Journal Article
• Language: English
• Published: New York, NY Springer 2006; Springer Nature B.V
• Subjects: Animals; Antineoplastic Agents - chemistry; Antineoplastic Agents - isolation & purification; Antineoplastic Agents - pharmacology; Apoptosis; Apoptosis - drug effects; Cancer; Cell Survival; Chromatography; DNA - genetics; Epidermal growth factor; Flow Cytometry; Genes, p53 - genetics; Indicators and Reagents; Magnetic Resonance Spectroscopy; Mice; NF-kappa B - genetics; NMR; Nuclear magnetic resonance; Structure-Activity Relationship; Transcription Factor AP-1 - genetics; Ubiquinone - analogs & derivatives; Ubiquinone - chemistry; Ubiquinone - isolation & purification; Ubiquinone - pharmacology; Urochordata - chemistry; United States > US; Russia
• ISSN: 0724-8741; 1573-904X
• DOI: 10.1007/s11095-005-8813-4

3-Demethylubiquinone Q2 was isolated from the ascidian Aplidium glabrum. The cancer-preventive properties and the structure-activity relationship for 3-demethylubiquinone Q2 and 12 of its synthetic analogs are reported. Compounds, having one or several di- or triprenyl substitutions and quinone moieties with methoxyls in different positions, were synthesized. The cancer-preventive properties of compounds and were tested in JB6 Cl41 mouse skin cells, using a variety of assessments, including the methanethiosulfonate (MTS) assay, flow cytometry, and soft agar assay. Statistical nonparametric methods were used to confirm statistical significance. All quinones tested were shown to inhibit JB6 Cl41 cell transformation, to induce apoptosis, AP-1, and NF-kappaB activity, and to inhibit p53 activity. The most promising effects were indicated for compounds containing two isoprene units in a side chain and a methoxyl group at the para-position to a polyprenyl substitution. Quinones and demonstrated cancer-preventive activity in JB6 Cl41 cells, which may be attributed to the induction of p53-independent apoptosis. These activities depended on the length of side chains and on the positions of the methoxyl groups in the quinone part of the molecule.