Antitumor Activity of Lankacidin Group Antibiotics Is Due to Microtubule Stabilization via a Paclitaxel-like Mechanism

被引:21
作者
Ayoub, Ahmed Taha [1 ,7 ]
Abou El-Magd, Rabab M. [2 ,8 ]
Xiao, Jack [3 ]
Lewis, Cody Wayne [2 ,9 ]
Tilli, Tatiana Martins [4 ]
Arakawa, Kenji [5 ]
Nindita, Yosi [5 ]
Chan, Gordon [2 ]
Sun, Luxin [6 ]
Glover, Mark [6 ]
Klobukowski, Mariusz [1 ]
Tuszynski, Jack [2 ]
机构
[1] Univ Alberta, Dept Chem, Edmonton, AB T6G 2G2, Canada
[2] Univ Alberta, Cross Canc Inst, Dept Oncol, Edmonton, AB T6G 1Z2, Canada
[3] Univ Alberta, Dept Elect & Comp Engn, Edmonton, AB T6G 1H9, Canada
[4] Natl Inst Sci & Technol Innovat Neglected Dis, BR-21040361 Rio De Janeiro, Brazil
[5] Hiroshima Univ, Grad Sch Adv Sci Matter, Dept Mol Biotechnol, Hiroshima 7398530, Japan
[6] Univ Alberta, Dept Biochem, Edmonton, AB T6G 2H7, Canada
[7] Heliopolis Univ, Dept Med Chem, Cairo 11777, Egypt
[8] City Sci Res & Technol Applicat, Alexandria 21934, Egypt
[9] Univ Alberta, Canc Res Inst Northern Alberta, Edmonton, AB T6G 2J7, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
GROUP T-2636 ANTIBIOTICS; AMBER FORCE-FIELD; PARAMETERS; REVEALS; COMPLEX; MICE;
D O I
10.1021/acs.jmedchem.6b01264
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Lankacidin group antibiotics show strong antimicrobial activity against various Gram-positive bacteria. In addition, they were shown to have considerable antitumor activity against certain cell line models. For decades, the antitumor activity of lankacidin was associated with the mechanism of its antimicrobial action, which is interference with peptide bond formation during protein synthesis. This, however, was never confirmed experimentally. Due to significant similarity to paclitaxel-like hits in a previous computational virtual screening study, we suggested that the cytotoxic effect of lankacidin is due to a paclitaxel-like action. In this study, we tested this hypothesis computationally and experimentally and confirmed that lankacidin is a microtubule stabilizer that enhances tubulin assembly and displaces taxoids from their binding site. This study serves as a starting point for optimization of lankacidin derivatives for better antitumor activities. It also highlights the power of computational predictions and their aid in guiding experiments and formulating rigorous hypotheses.
引用
收藏
页码:9532 / 9540
页数:9
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