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Study of cytotoxicity of spiro-fused [3-azabicyclo[3.1.0]hexane]oxindoles against tumor cell lines
1 , 1 , 1 , 1 , 2 , * 3
1  Saint Petersburg National Research Academic University of the Russian Academy of Sciences
2  Saint Petersburg State University
3  Saint Petersburg National Research Academic University of the Russian Academy of Sciences, Saint Petersburg, Russia
Academic Editor: Duke Wang


Oncological diseases are one of the most common public health problems and second leading cause of death after cardiovascular disease. Natural products or synthetic compounds inspired from natural products continue to be excellent sources for new drug candidates. Recent advances in synthesis of complex heterocyclic systems have led to significant increase in interest in development of efficient methods for synthesis of thereof as potential drugs or biological probes. Oxindole, azabicyclohexane and pyrrolizine units are known heterocyclic motifs that form core of a large family of alkaloid natural products with strong bioactivity profiles.

Series of heterocyclic compounds containing 3-spiro[3-azabicyclo[3.1.0]hexane]oxindole framework have been studied for their antiproliferative activity against K562, Jurkat, HeLa, CT26 cell lines. This spiro-fused adducts are readily available via one-pot three-component 1,3-dipolar cycloaddition reactions of cyclopropenes and azomethine ylides (generated in situ from amino acids and oxindoles). In agreement with DNA cytometry studies, the tested compounds have achieved significant cell-cycle perturbation with higher accumulation of cells in G0/G1 phase. Using confocal microscopy, we found that actin filaments disappeared and granular actin was distributed diffusely in the cytoplasm in up to 40% of treated cells. Also we discovered that number of cells with filopodium-like membrane protrusions was significantly reduced after treatment with some of tested compounds (from 92 % in control cells up to 36% after treatment). The obtained results support the antitumor effect of the studied compounds and encourage the extension of the study in order to improve the anticancer activity and reduce the toxicological risks of obtained compounds.

Keywords: antiproliferative activity; tumor cell lines; morphological changes (cytoskeleton); cell death; cell cycle; spiro-fused [3-azabicyclo[3.1.0]hexane]oxindoles