Department of Clinical Biochemistry, Faculty of Medicine, 113380Mashhad University of Medical Sciences, Mashhad, Iran.
Cardiovascular Diseases Research Center, 196469Birjand University of Medical Sciences, Birjand, Iran.
Int J Toxicol. 2022 Sep-Oct;41(5):402-411. doi: 10.1177/10915818221104417. Epub 2022 Jun 19.
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 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.
结直肠癌(CRC)是全球癌症相关死亡的第二大原因。最近,草药药物,特别是姜烯,已被广泛研究和用于癌症治疗,因为它们具有显著的抗癌作用。然而,关于姜烯在 CRC 中的抗癌作用的信息有限。因此,我们旨在研究姜烯在 CRC 中的抗癌作用,重点研究细胞凋亡和迁移。使用 MTT 和划痕愈合试验分别评估姜烯对 HT-29 细胞的抗增殖和抗迁移作用。通过定量实时 PCR(qRT-PCR)测定迁移和凋亡相关基因的 mRNA 表达水平。通过流式细胞术评估细胞凋亡和细胞周期分布。使用 ROS 测定试剂盒测量细胞内活性氧(ROS)水平。此外,使用明胶酶谱法测定基质金属蛋白酶-2/-9(MMP-2/-9)的活性。姜烯以剂量依赖性方式抑制 HT-29 细胞的活力,而对正常 NIH/3T3 细胞的细胞毒性较小。姜烯诱导 HT-29 细胞凋亡并将细胞周期阻滞在 G2/M 期。这些作用与凋亡相关基因表达的改变(Bax 上调和 Bcl-2 基因下调)有关。姜烯还增强了 HT-29 细胞中 ROS 的产生。此外,姜烯显著抑制 HT-29 细胞的迁移,并降低 MMP-2/-9 mRNA 表达和活性。我们的研究结果为姜烯在 HT-29 细胞中诱导凋亡和抑制转移提供了一种潜在的用途;因此,它可以开发为未来 CRC 治疗的有前途的天然药物。