Tumor-Inhibitory Effects of Zerumbone Against HT-29 Human Colorectal Cancer Cells

细胞凋亡 活力测定 细胞周期 癌细胞 流式细胞术 活性氧 基质金属蛋白酶 癌症 MTT法 结直肠癌 癌症研究 化学 分子生物学 生物 药理学 细胞生物学 生物化学 遗传学
作者
Fezzeh Memari,Farshad Mirzavi,Mohammad Jalili‐Nik,Amir R. Afshari,Ahmad Ghorbani,Mohammad Soukhtanloo
出处
期刊:International Journal of Toxicology [SAGE Publishing]
卷期号:41 (5): 402-411 被引量:22
标识
DOI:10.1177/10915818221104417
摘要

Colorectal cancer (CRC) is the second cause of cancer-associated death globally. Recently, herbal medicinal products and, in particular, zerumbone have been widely studied and used for cancer treatment as they induce significant anti-cancer effects. However, there is limited information about the anti-cancer effects of zerumbone in CRC. Therefore, we aimed to investigate the in vitro anti-cancer effects of the zerumbone in CRC, focusing on cell apoptosis and migration. Anti-proliferative and anti-migratory effects of zerumbone on HT-29 cells were evaluated using MTT and scratch wound healing assay, respectively. Quantitative real-time PCR (qRT-PCR) was performed to determine the mRNA expression levels of migration and apoptosis-related genes. Apoptosis and cell cycle distribution were evaluated by flow cytometry. The intracellular level of reactive oxygen species (ROS) was measured using a ROS assay kit. Additionally, matrix metalloproteinase-2/-9 (MMP-2/-9) activity was determined using gelatin zymography. Zerumbone suppressed the viability of the HT-29 cells dose-dependently while having less cytotoxicity on normal NIH/3T3 cells. Zerumbone induced apoptosis in HT-29 cells and arrested the cell cycle in the G2/M phase. These effects were associated with alteration in the expression of apoptosis-related genes (up-regulation of Bax and down-regulation of Bcl-2 genes). Zerumbone also enhanced the generation of ROS in HT-29 cells. Furthermore, zerumbone significantly inhibited the migration of HT-29 cells and decreased MMP-2/-9 mRNA expression and activity. Our findings provide a potential use for zerumbone to induce apoptosis and suppress metastasis in HT-29 cells; thus, it could be developed as a promising natural agent for future CRC therapy.
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