TY - JOUR
T1 - Maytansinoids in cancer therapy
T2 - advancements in antibody–drug conjugates and nanotechnology-enhanced drug delivery systems
AU - Perra, Matteo
AU - Castangia, Ines
AU - Aroffu, Matteo
AU - Fulgheri, Federica
AU - Abi-Rached, Rita
AU - Manca, Maria Letizia
AU - Cortés, Hernán
AU - Del Prado-Audelo, María Luisa
AU - Nomura-Contreras, Carla
AU - Romero-Montero, Alejandra
AU - Büsselberg, Dietrich
AU - Leyva-Gómez, Gerardo
AU - Sharifi-Rad, Javad
AU - Calina, Daniela
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/12
Y1 - 2025/12
N2 - Cancer remains the second leading cause of death globally, driving the need for innovative therapies. Among natural compounds, maytansinoids have shown significant promise, contributing to nearly 25% of recently approved anticancer drugs. Despite their potential, early clinical trials faced challenges due to severe side effects, prompting advancements in delivery systems such as antibody-maytansinoid conjugates (AMCs). This review highlights the anticancer activity of maytansinoids, with a focus on AMCs designed to target cancer cells specifically. Preclinical and clinical studies show that AMCs, including FDA-approved drugs like Kadcyla and Elahere, effectively inhibit tumor growth while reducing systemic toxicity. Key developments include improved synthesis methods, linker chemistry and payload design. Ongoing research aims to enhance the safety and efficacy of AMCs, integrate nanotechnology for drug delivery, and identify novel therapeutic targets. These advancements hold potential to transform maytansinoid-based cancer treatments in the future.
AB - Cancer remains the second leading cause of death globally, driving the need for innovative therapies. Among natural compounds, maytansinoids have shown significant promise, contributing to nearly 25% of recently approved anticancer drugs. Despite their potential, early clinical trials faced challenges due to severe side effects, prompting advancements in delivery systems such as antibody-maytansinoid conjugates (AMCs). This review highlights the anticancer activity of maytansinoids, with a focus on AMCs designed to target cancer cells specifically. Preclinical and clinical studies show that AMCs, including FDA-approved drugs like Kadcyla and Elahere, effectively inhibit tumor growth while reducing systemic toxicity. Key developments include improved synthesis methods, linker chemistry and payload design. Ongoing research aims to enhance the safety and efficacy of AMCs, integrate nanotechnology for drug delivery, and identify novel therapeutic targets. These advancements hold potential to transform maytansinoid-based cancer treatments in the future.
KW - Antibody-maytansinoid conjugates
KW - Anticancer studies
KW - Maytansine
KW - Maytansinoid-based therapies
KW - Microtubules polymerization inhibitors
KW - Natural compounds
UR - https://www.scopus.com/pages/publications/85218138030
U2 - 10.1007/s12672-025-01820-z
DO - 10.1007/s12672-025-01820-z
M3 - Artículo de revisión
AN - SCOPUS:85218138030
SN - 1868-8497
VL - 16
JO - Discover Oncology
JF - Discover Oncology
IS - 1
M1 - 73
ER -