Induction of Apoptosis by Cynaropicrin in Human Colon Cancer Cell Line HCT-116 through the Mitochondria-mediated Apoptotic Pathway

IF 0.6 4区 医学 Q4 CHEMISTRY, MEDICINAL Pharmacognosy Magazine Pub Date : 2023-09-13 DOI:10.1177/09731296231183833
Lei Wang, Xiaoqin Bie, Suresh Mickymaray, Abdulaziz S. Alothaim, Yan Pei, Huaping Gong
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Abstract

Background Colon cancer continues to be the third most commonly occurring cancer around the globe with both lifestyle-related risk factors and genetic dispositions. Owing to the increased incidence of the disease, there is a need to find new treatment options which are easily accessible and less toxic to the cells. Cynaropicrin, a sesquiterpene extract from the artichoke plant exhibits varied properties such as anti-inflammatory, anti-cancer, and antioxidant among others. In the current investigation, the anti-cancer potential of the cynaropicrin extract was observed against colon cancer in HCT-116 cell lines. Materials and Methods The drug exhibited a considerable decrease in cell proliferation. Also analyzed was the reactive oxygen species (ROS) generation and apoptosis induction by cynaropicrin on the HCT-116 cell line. The AO/EtBr staining confirmed the apoptotic induction through chromatin condensation by fluorescence microscopic examination followed by DAPI staining of the treated HCT-116 cells which showed nuclear condensation and disintegration. Results Furthermore, it was observed that cynaropicrin elevated the levels of ROS in the cells which modified the mitochondrial membrane permeability in the HCT-116 cell lines. The study also evaluated the levels of apoptotic proteins and the expression of inflammatory cytokines concerning cells treated with cynaropicrin and untreated control cells. Conclusion It has been observed that cynaropicrin treatment can lead to apoptosis in the HCT-116 cell line via mitochondria-mediated apoptotic pathway and if further evaluated, it can turn out to be a potent anti-cancer drug for effective management of colon cancer.
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Cynaropicrin通过线粒体介导的凋亡途径诱导人结肠癌细胞系HCT-116凋亡
结肠癌仍然是全球第三大常见癌症,与生活方式相关的风险因素和遗传倾向有关。由于该病发病率增加,有必要寻找易于获得且对细胞毒性较小的新治疗办法。Cynaropicrin是一种从朝鲜蓟植物中提取的倍半萜素,具有多种特性,如抗炎、抗癌和抗氧化等。本研究在HCT-116细胞系中观察了苦辛酸提取物对结肠癌的抗癌作用。材料与方法该药物能显著抑制细胞增殖。并分析了cynaropicrin对HCT-116细胞株的活性氧(ROS)生成及诱导凋亡的作用。AO/EtBr染色证实HCT-116细胞通过荧光显微镜观察染色质凝集诱导凋亡,DAPI染色显示细胞核凝集和解体。结果cynaropicrin可提高细胞内ROS水平,改变HCT-116细胞系线粒体膜通透性。该研究还评估了cynaropicrin处理的细胞和未处理的对照细胞的凋亡蛋白水平和炎症细胞因子的表达。结论cynaropicrin可通过线粒体介导的凋亡途径导致HCT-116细胞凋亡,如果进一步研究,cynaropicrin可能成为一种有效治疗结肠癌的有效抗癌药物。
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来源期刊
Pharmacognosy Magazine
Pharmacognosy Magazine CHEMISTRY, MEDICINAL-
CiteScore
1.87
自引率
0.00%
发文量
37
审稿时长
3 months
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