New insights into the anticancer therapeutic potential of maytansine and its derivatives

被引:19
|
作者
Zafar, Sameen [1 ]
Armaghan, Muhammad [1 ]
Khan, Khushbukhat [1 ]
Hassan, Nazia [2 ]
Sharifi-Rad, Javad [3 ]
Habtemariam, Solomon [4 ]
Kieliszek, Marek [5 ]
Butnariu, Monica [6 ]
Bagiu, Iulia-Cristina [7 ,8 ]
Bagiu, Radu Vasile [7 ,9 ]
Cho, William C. [10 ]
机构
[1] Natl Univ Sci & Technol, Atta ur Rahman Sch Appl Biosci, Dept Healthcare Biotechnol, Islamabad, Punjab, Pakistan
[2] Univ Agr Faisalabad, Dept Biochem, Faisalabad, Pakistan
[3] Univ Azuay, Fac Med, Cuenca, Ecuador
[4] Univ Greenwich, Pharmacognosy Res & Herbal Anal Serv UK, Cent Ave, Chatham ME4 4TB, Kent, England
[5] Warsaw Univ Life Sci SGGW, Inst Food Sci, Dept Food Biotechnol & Microbiol, Nowoursynowska 159 C, PL-02776 Warsaw, Poland
[6] Univ Life Sci King Mihai I Timisoara, Calea Aradului 119, Timis 300645, Romania
[7] Victor Babes Univ Med, Dept Microbiol, Pharm Timisoara, Timisoara, Romania
[8] Multidisciplinary Res Ctr Antimicrobial Resistanc, Timisoara, Romania
[9] Prevent Med Study Ctr, Timisoara, Romania
[10] Queen Elizabeth Hosp, Dept Clin Oncol, Kowloon, Peoples R China
关键词
Maytansine; Derivatives; Antibody-drug conjugate; Cytotoxicity; Anticancer activity; Tubulin instability; ANTIBODY-DRUG CONJUGATE; TRASTUZUMAB EMTANSINE T-DM1; IN-VIVO ACTIVITY; ANTITUMOR-ACTIVITY; MEDICINAL-PLANTS; CANCER STATISTICS; NATURAL COMPOUNDS; TUMOR INHIBITORS; TREWIA-NUDIFLORA; MAYTENUS;
D O I
10.1016/j.biopha.2023.115039
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Maytansine is a pharmacologically active 19-membered ansamacrolide derived from various medicinal plants and microorganisms. Among the most studied pharmacological activities of maytansine over the past few decades are anticancer and anti-bacterial effects. The anticancer mechanism of action is primarily mediated through interaction with the tubulin thereby inhibiting the assembly of microtubules. This ultimately leads to decreased stability of microtubule dynamics and cause cell cycle arrest, resulting in apoptosis. Despite its potent pharmacological effects, the therapeutic applications of maytansine in clinical medicine are quite limited due to its non-selective cytotoxicity. To overcome these limitations, several derivatives have been designed and developed mostly by modifying the parent structural skeleton of maytansine. These structural derivatives exhibit improved pharmacological activities as compared to maytansine. The present review provides a valuable insight into maytansine and its synthetic derivatives as anticancer agents.
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页数:16
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