TY - JOUR
T1 - Novel Resveratrol-Based Aspirin Prodrugs
T2 - Synthesis, Metabolism, and Anticancer Activity
AU - Zhu, Yingdong
AU - Fu, Junsheng
AU - Shurlknight, Kelly L.
AU - Soroka, Dominique N.
AU - Hu, Yuhui
AU - Chen, Xiaoxin
AU - Sang, Shengmin
N1 - Publisher Copyright:
© 2015 American Chemical Society.
PY - 2015/8/27
Y1 - 2015/8/27
N2 - (Graph Presented). Regular aspirin use has been convincingly shown to reduce the risk of colorectal cancer. However, long-term use of aspirin leads to gastrotoxicity. Herein, we designed and synthesized a novel class of resveratrol-based aspirin prodrugs to simultaneously release aspirin and resveratrol to attenuate the side effects caused by aspirin. Prodrug RAH exerted enhanced anticancer activities which are better than a physical mixture of aspirin and resveratrol as well as each individually. Metabolism of RAH in mice showed that the majority of RAH is decomposed to release resveratrol and aspirin or salicylic acid either in the intestine or after absorption. Mechanistic studies demonstrate RAH inhibits cell cycle arrest through downregulation of cyclins and induces apoptosis by activation of caspase-3 in cancer cells. These findings highlighted the improved anticancer properties of resveratrol-based aspirin prodrugs. RAH may represent novel and safe alternatives of aspirin for the purpose of daily use in the future.
AB - (Graph Presented). Regular aspirin use has been convincingly shown to reduce the risk of colorectal cancer. However, long-term use of aspirin leads to gastrotoxicity. Herein, we designed and synthesized a novel class of resveratrol-based aspirin prodrugs to simultaneously release aspirin and resveratrol to attenuate the side effects caused by aspirin. Prodrug RAH exerted enhanced anticancer activities which are better than a physical mixture of aspirin and resveratrol as well as each individually. Metabolism of RAH in mice showed that the majority of RAH is decomposed to release resveratrol and aspirin or salicylic acid either in the intestine or after absorption. Mechanistic studies demonstrate RAH inhibits cell cycle arrest through downregulation of cyclins and induces apoptosis by activation of caspase-3 in cancer cells. These findings highlighted the improved anticancer properties of resveratrol-based aspirin prodrugs. RAH may represent novel and safe alternatives of aspirin for the purpose of daily use in the future.
UR - https://www.scopus.com/pages/publications/84940476354
U2 - 10.1021/acs.jmedchem.5b00536
DO - 10.1021/acs.jmedchem.5b00536
M3 - Article
SN - 0022-2623
VL - 58
SP - 6494
EP - 6506
JO - Journal of Medicinal Chemistry
JF - Journal of Medicinal Chemistry
IS - 16
ER -