3,3′,5,5′-tetramethoxybiphenyl-4,4′diol induces cell cycle arrest in G2/M phase and apoptosis in human non-small cell lung cancer A549 cells

细胞凋亡 A549电池 活力测定 细胞周期 程序性细胞死亡 细胞周期检查点 细胞毒性T细胞 癌症研究 生物 细胞培养 流式细胞术 化学 细胞生物学 分子生物学 生物化学 体外 遗传学
作者
Vírgínia Márcia Concato,Fernanda Tomiotto-Pellissier,Taylon Felipe Silva,Manoela Daiele Gonçalves,Bruna Taciane da Silva Bortoleti,Mariana Barbosa Detoni,Elaine da Silva Siqueira,Ana Carolina Jacob Rodrigues,Jéseka G. Schirmann,Aneli M. Barbosa-Dekker,Idessânia Nazareth Costa,Ivete Conchon‐Costa,Milena Menegazzo Miranda-Sapla,Mário Mantovani,Wander Rogério Pavanelli
出处
期刊:Chemico-Biological Interactions [Elsevier BV]
卷期号:326: 109133-109133 被引量:11
标识
DOI:10.1016/j.cbi.2020.109133
摘要

Lung cancer is one of the leading causes of cancer-related death worldwide. It has aggressive manifestation, high ability to promote metastasis and late diagnosis. In the present study, we investigated the cytotoxic effect of 3,3′,5,5′-tetramethoxybiphenyl-4,4′diol (TMBP), against the A549 human non-small cell lung carcinoma lineage. The A549 cell line was treated for 72h with TMBP (12.5–200 μM) with and subsequently defined the 50% inhibitory concentration (148 μM ± 0.05), from which tests were performed to determine the viability, volume, and regulation of the cell cycle. Finally, we investigated the death mechanisms involved in the action of the treatments by flow cytometry and fluorimetry. The TMBP-treatment of primary cells, peritoneal macrophages, and sheep erythrocytes did not reduce the viability of these cells. On the other hand, TMBP was able to reduce the viability of the investigated cell line, by cytotoxic action and to promote the reduction of cell size. Subsequently, we found that TMBP treatment was able to increase the production of reactive oxygen species, cause mitochondrial depolarization, induce cell cycle arrest in G2/M phase and lead to death by direct apoptosis. Thus, this study revealed that TMBP could be a promising candidate for the development of antitumor drugs targeting lung cancer.
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