3,5-Bis(2-Trifluomethoxybenzylidene)-4-Piperidone Induces Apoptosis in A549 Cells Through Reactive Oxygen Species-Mediated Pathways


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Аннотация

Medicines with the F3C-O group can increase the lipophilicity of an aromatic ring system and protect it from oxidative attacks. We have synthesized 3,5-bis(2-trifluomethoxybenzylidene)-4-piperidone (4a), an EF24 analog with ortho trifluoromethoxy group, via aldol condensation reaction and evaluated its cytotoxicity by MTT assay. Owning to the ortho-trifluoromethoxy group, compound 4a exhibited excellent cytotoxicity against A549 cells. Mechanistic investigation indicated that 4a could induce oxidative stress, including the generation of reactive oxygen species (ROS), imbalance of redox buffering system, lipid peroxidation, and collapse of mitochondrial membrane potential, and finally leading to cell apoptosis. These data indicated that the introduction of the ortho-trifluoromethoxy group into curcumin analogs may be an effective strategy to enhance the anti-cancer ROS based activity.

Об авторах

Jie Yang

School of Pharmacy, Liaocheng University

Автор, ответственный за переписку.
Email: yangjie1110@163.com
Китай, 1 Hunan Street, Liaocheng, Shandong, 252000

Su-Su Meng

School of Pharmacy, Liaocheng University

Email: yangjie1110@163.com
Китай, 1 Hunan Street, Liaocheng, Shandong, 252000

Yong-Jing Zhao

School of Pharmacy, Liaocheng University

Email: yangjie1110@163.com
Китай, 1 Hunan Street, Liaocheng, Shandong, 252000

Guang-Yong Li

School of Pharmacy, Liaocheng University

Email: yangjie1110@163.com
Китай, 1 Hunan Street, Liaocheng, Shandong, 252000

Ling-Yun Ge

School of Pharmacy, Liaocheng University

Email: yangjie1110@163.com
Китай, 1 Hunan Street, Liaocheng, Shandong, 252000

Hua-Lei Zhang

School of Pharmacy, Liaocheng University

Email: yangjie1110@163.com
Китай, 1 Hunan Street, Liaocheng, Shandong, 252000

Guo-Yun Liu

School of Pharmacy, Liaocheng University

Email: yangjie1110@163.com
Китай, 1 Hunan Street, Liaocheng, Shandong, 252000


© Springer Science+Business Media, LLC, part of Springer Nature, 2019

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