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Triterpene Glycosides from the Sea Cucumber Ocnus glacialis Display Cytotoxic and Colony-Inhibiting Activity Against
Alexandra S Silchenko1, Ekaterina A Chingizova1, Ekaterina S Menchinskaya1
1G.B. Elyakov Pacific Institute of Bioorganic Chemistry, Far Eastern Branch of the Russian Academy of Sciences, Pr. 100-Letya Vladivostoka 159, 690022 Vladivostok, Russia.
Abstract:
As a result of investigation of glycosidic composition of the sea cucumber Ocnus glacialis (Cucumariidae, Dendrochirotida) two new glycosides, glacialisosides A (1) and B (2), were isolated. Their structures were established by in-depth analysis of 1H, 13C NMR, 1D TOCSY, and 2D NMR (1H,1H COSY, HMBC, HSQC, ROESY), in addition to HR-ESI mass spectra. The structures of the obtained desulfated derivatives 3, 4 were elucidated by HR-ESI-MS and ESI-MS/MS. The aglycone moieties of these glycosides are known from other glycosides of four species belonging to the order Dendrochirotida. However, despite sharing common sugar compositions and architectures, the carbohydrate chains of 1, 2 are novel due to the distinct positioning of sulfate groups. Glacialisosides A (1) and B (2) exhibit structural features shared with compounds from sea cucumbers of the orders Holothuriida, Elasipodida, and Dendrochirotida. The hemolytic and cytotoxic activities of compounds 1-4 were studied against human erythrocytes and four breast cancer cell lines (MCF-7, T-47D, MDA-MB-231, and MDA-MB-468), as well as the non-tumorigenic mammary epithelial cell line MCF-10A and the pancreatic epithelioid carcinoma cell line PANC-1. The sulfated native compounds 1 and 2 were significantly more potent than desulfated derivatives 3 and 4 across all tested cell lines, indicating a positive contribution of sulfate groups to bioactivity. Notably, the normal epithelial MCF-10A cells exhibited resistance to the membranolytic action of the glycosides, an important and favorable feature, particularly given the pronounced cytotoxicity observed against the triple-negative MDA-MB-231 cell line. Furthermore, glacialisoside A (1) demonstrated potent inhibitory activity against the formation and growth of MDA-MB-468 cell colonies, effectively blocking cell division even at concentrations below 0.2 μM and completely halting it at a dosage of 1 μM. Thus, the colony formation assay reveals a latent sensitivity of cancer cells-not only to the membranolytic action of triterpene glycosides, but also to the effects of these compounds relevant to other aspects of cell survival, division, and spread.
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