G.B. Elyakov Pacific Institute of Bioorganic Chemistry, Far Eastern Branch of the Russian Academy of Sciences, 159 100-let Vladivostok Ave., 690022 Vladivostok, Russia.
Mar Drugs. 2021 Sep 25;19(10):540. doi: 10.3390/md19100540.
Colorectal cancer is one of the most frequent types of malignancy in the world. The search for new approaches of increasing the efficacy of cancer therapy is relevant. This work was aimed to study individual, combined anticancer effects, and molecular mechanism of action of sulfated laminaran AaLs of the brown alga and protolinckiosides A (PL1), B (PL2), and linckoside L1 (L1) of the starfish using a 3D cell culture model. The 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium (MTS), soft agar, 3D spheroids invasion, and Western blotting assays were performed to determine the effect and mechanism of the action of investigated compounds or their combinations on proliferation, colony formation, and the invasion of 3D HCT 116 spheroids. AaLs, PL1, PL2, and L1 individually inhibited viability, colony growth, and the invasion of 3D HCT 116 spheroids in a variable degree with greater activity of linckoside L1. AaLs in combination with L1 exerted synergism of a combined anticancer effect through the inactivation of protein kinase B (AKT) kinase and, consequently, the induction of apoptosis via the regulation of proapoptotic/antiapoptotic proteins balance. The obtained data about the efficacy of the combined anticancer effect of a laminaran derivative of brown algae and polyhydroxysteroid glycosides of starfish open up prospects for the development of new therapeutic approaches for colorectal cancer treatment.
结直肠癌是世界上最常见的恶性肿瘤之一。寻找提高癌症治疗疗效的新方法是相关的。这项工作旨在研究褐藻硫酸化岩藻聚糖 AaLs 与海星多羟基甾醇糖苷普罗林克糖苷 A(PL1)、B(PL2)和林克糖苷 L1(L1)的单独、联合抗癌作用及其分子作用机制,采用 3D 细胞培养模型。通过 3-(4,5-二甲基噻唑-2-基)-5-(3-羧基甲氧基苯基)-2-(4-磺苯基)-2H-四唑(MTS)、软琼脂、3D 球体侵袭和 Western blot 测定来确定研究化合物或其组合对增殖、集落形成和 3D HCT 116 球体侵袭的影响和作用机制。 AaLs、PL1、PL2 和 L1 单独抑制了 3D HCT 116 球体的活力、集落生长和侵袭,其中林克糖苷 L1 的活性更强。 AaLs 与 L1 联合使用通过使蛋白激酶 B(AKT)激酶失活,并通过调节促凋亡/抗凋亡蛋白平衡诱导细胞凋亡,从而发挥协同的抗癌作用。关于褐藻岩藻聚糖衍生物和海星多羟基甾醇糖苷联合抗癌作用的有效性的获得的数据为结直肠癌治疗的新治疗方法的发展开辟了前景。