柚皮苷可诱导鼻咽癌细胞在 ROS 刺激下进入 G1 细胞周期并导致凋亡

IF 4.4 3区 医学 Q2 ENVIRONMENTAL SCIENCES Environmental Toxicology Pub Date : 2024-07-26 DOI:10.1002/tox.24378
Chan-Hung Chen, Ni Tien, Chun-Hsu Yao, Siang-Jyun Chen, Da-Tian Bau, Sudhir Pandey, Hsin-Ling Yang, You-Cheng Hseu, Shih-Shun Chen, Meng-Liang Lin
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引用次数: 0

摘要

柚皮苷是一种来自葡萄柚或柑橘的生物类黄酮化合物,对宫颈癌、甲状腺癌、结肠癌、脑癌、肝癌、肺癌、甲状腺癌和乳腺癌具有抗癌活性。本研究旨在探索柚皮苷对鼻咽癌细胞的抗癌作用。柚皮苷对 NPC-TW 039 和 NPC-TW 076 细胞有细胞毒性作用,24 或 48 小时的 IC50 分别为 372/328 和 394/307 μM,而对正常牙龈上皮(SG)细胞的毒性很小(>500/500 μM)。我们证实,柚皮苷是通过抑制 NPC 细胞中的细胞周期蛋白 D1、细胞周期蛋白 A 和 CDK2 以及上调 p21 蛋白来引发 G1 期停滞的。将鼻咽癌细胞暴露于柚皮苷可导致一系列凋亡事件,包括形态变化(细胞缩小和膜裂开)和染色质凝集。Annexin V 和 PI 染色表明,柚皮素处理可促进鼻咽癌细胞坏死和晚期凋亡。DiOC6 染色显示,柚皮素处理会导致线粒体膜电位下降,继而导致细胞色素 c 释放、Apaf-1/caspase-9/-3 激活、PARP 裂解以及鼻咽癌细胞中 EndoG 的表达。柚皮素可上调促凋亡 Bax 的表达,降低抗凋亡 Bcl-xL 的表达,并导致鼻咽癌细胞中 Bax/Bcl-xL 比率失调。值得注意的是,柚皮素增强了与死亡受体相关的 t-Bid 的表达。此外,柚皮苷处理增加了 Ca2+ 的释放,通过增加鼻咽癌细胞中 IRE1、ATF-6、GRP78、GADD153 和 caspase-12 的表达,诱发了内质网应激相关的细胞凋亡。此外,柚皮苷会引发 ROS 生成,而抗氧化剂 N- 乙酰半胱氨酸可抑制柚皮苷诱导的 ROS 生成,从而防止鼻咽癌细胞 G1 期停滞和凋亡。柚皮苷诱导的 ROS 介导的 G1 期停滞和线粒体、死亡受体及内质网应激介导的细胞凋亡可能是一种治疗鼻咽癌的有效策略。
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Naringin Induces ROS-Stimulated G1 Cell-Cycle Arrest and Apoptosis in Nasopharyngeal Carcinoma Cells

Naringin, a bioflavonoid compound from grapefruit or citrus, exerts anticancer activities on cervical, thyroid, colon, brain, liver, lung, thyroid, and breast cancers. The present investigation addressed exploring the anticancer effects of naringin on nasopharyngeal carcinoma (NPC) cells. Naringin exhibits a cytotoxic effect on NPC-TW 039 and NPC-TW 076 cells with IC50 372/328 and 394/307 μM for 24 or 48 h, respectively, while causing little toxicity toward normal gingival epithelial (SG) cells (>500/500 μM). We established that naringin triggered G1 arrest is achieved by suppressing cyclin D1, cyclin A, and CDK2, and upregulating p21 protein in NPC cells. Exposure of NPC cells to naringin caused a series of events leading to apoptosis including morphology change (cell shrinkage and membrane blebbing) and chromatin condensation. Annexin V and PI staining indicated that naringin treatment promotes necrosis and late apoptosis in NPC cells. DiOC6 staining showed a decline in the mitochondrial membrane potential by naringin treatment, which was followed with cytochrome c release, Apaf-1/caspase-9/-3 activation, PARP cleavage, and EndoG expression in NPC cells. Naringin upregulated proapoptotic Bax and decreased antiapoptotic Bcl-xL expression, and dysregulated Bax/Bcl-xL ratio in NPC cells. Notably, naringin enhanced death receptor-related t-Bid expression. Furthermore, an increased Ca2+ release by naringin treatment which instigated endoplasmic reticulum stress-associated apoptosis through increased IRE1, ATF-6, GRP78, GADD153, and caspase-12 expression in NPC cells. In addition, naringin triggers ROS production, and inhibition of naringin-induced ROS generation by antioxidant N-acetylcysteine resulted in the prevention of G1 arrest and apoptosis in NPC cells. Naringin-induced ROS-mediated G1 arrest and mitochondrial-, death receptor-, and endoplasmic reticulum stress–mediated apoptosis may be a promising strategy for treating NPC.

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来源期刊
Environmental Toxicology
Environmental Toxicology 环境科学-毒理学
CiteScore
7.10
自引率
8.90%
发文量
261
审稿时长
4.5 months
期刊介绍: The journal publishes in the areas of toxicity and toxicology of environmental pollutants in air, dust, sediment, soil and water, and natural toxins in the environment.Of particular interest are: Toxic or biologically disruptive impacts of anthropogenic chemicals such as pharmaceuticals, industrial organics, agricultural chemicals, and by-products such as chlorinated compounds from water disinfection and waste incineration; Natural toxins and their impacts; Biotransformation and metabolism of toxigenic compounds, food chains for toxin accumulation or biodegradation; Assays of toxicity, endocrine disruption, mutagenicity, carcinogenicity, ecosystem impact and health hazard; Environmental and public health risk assessment, environmental guidelines, environmental policy for toxicants.
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