Laboratory of Immunoparasitology of Neglected Diseases and Cancer, State University of Londrina, PR, Brazil.
Laboratory of Immunoparasitology of Neglected Diseases and Cancer, State University of Londrina, PR, Brazil; Graduate Program in Biosciences and Biotechnology, Carlos Chagas Institute (ICC), Fiocruz, Curitiba, PR, Brazil.
Chem Biol Interact. 2020 Aug 1;326:109133. doi: 10.1016/j.cbi.2020.109133. Epub 2020 May 24.
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.
肺癌是全球癌症相关死亡的主要原因之一。它具有侵袭性表现、高转移能力和晚期诊断。在本研究中,我们研究了 3,3',5,5'-四甲氧基联苯-4,4'-二醇(TMBP)对 A549 人非小细胞肺癌系的细胞毒性作用。A549 细胞系用 TMBP(12.5-200 μM)处理 72 小时,随后确定 50%抑制浓度(148 μM±0.05),从这些测试中确定细胞活力、体积和细胞周期的调节。最后,我们通过流式细胞术和荧光法研究了涉及治疗作用的死亡机制。TMBP 处理原代细胞、腹腔巨噬细胞和绵羊红细胞不会降低这些细胞的活力。另一方面,TMBP 能够通过细胞毒性作用降低被研究细胞系的活力,并促进细胞体积减小。随后,我们发现 TMBP 处理能够增加活性氧的产生、引起线粒体去极化、诱导 G2/M 期细胞周期停滞并导致直接凋亡死亡。因此,这项研究表明 TMBP 可能是开发针对肺癌的抗肿瘤药物的有前途的候选药物。