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来自[具体植物名称未给出,推测为T植物]的活性化合物对人肺癌细胞的生物活性及作用机制

Bioactivities and action mechanisms of active compounds from T on human lung cancer cells.

作者信息

Chen Yuh-Fung, Chang Wen-Hsin, Tsai Huei-Yann, Lee Min-Min, Wu Tian-Shang

机构信息

Department of Pharmacology, China Medical University, Taichung, Taiwan.

Department of Pharmacy, China Medical University Hospital, Taichung, Taiwan.

出版信息

Biomedicine (Taipei). 2021 Jun 1;11(2):40-46. doi: 10.37796/2211-8039.1219. eCollection 2021.

Abstract

BACKGROUND

Lung cancer is the leading cause of death in Taiwan for years. Besides the currently used chemotherapy, herbal medicine may play a role in the treatment of lung cancer. Thunb (HC), one of the frequently used herbal medicine in Taiwan, has been widely used in various diseases. Review from literatures, HC has many effects, including anti-inflammatory, anti-viral, anti-bacterial, anti-SARS, and anti-tumor activities. However, there is no literatures describe its active compounds on lung cancer. This present study aims to evaluate the possible effect and action mechanism of active compounds from HC (aristolactam BII, aristolactam AII, and noraristolodione) on lung cancer. A549 lung cancer cell line was used to evaluate the effects of HC on the cell viability and possible anti-tumor effects.

METHODS

We used A549 cells in the evaluation of anticancer activity. Cell viability, cell cycle, cell apoptosis and apoptosis related protein expression were studied.

RESULTS

Active compounds from HC significantly inhibited A549 cell viability and induced accumulation of cell cycle at S or G2/M phase on A549 cells in a concentration-dependent manner, and induced A549 arrest at S or G2/M phase via increasing p21, p27, p53 and reducing cyclin-E, -A, cyclin-dependent kinase 2 (CDK2), cdc-2 (CDK1) protein expression. Additionally, HC induced A549 cell late apoptosis by up-regulating caspase-3, -8, Bax and decreasing Bcl-2 protein expression.

CONCLUSIONS

The anti-tumor effects of aristolactam BII, aristolactam AII, and noraristolodione on human lung carcinoma A549 cells were via cell cycle arrest and apoptosis.

摘要

背景

多年来肺癌一直是台湾地区的主要死因。除了目前使用的化疗方法外,草药可能在肺癌治疗中发挥作用。台湾常用的草药之一土沉香(HC)已被广泛用于各种疾病。从文献综述来看,HC具有多种作用,包括抗炎、抗病毒、抗菌、抗非典和抗肿瘤活性。然而,尚无文献描述其对肺癌的活性化合物。本研究旨在评估HC中的活性化合物(马兜铃内酰胺BII、马兜铃内酰胺AII和去甲马兜铃二酮)对肺癌的可能作用及作用机制。使用A549肺癌细胞系评估HC对细胞活力和可能的抗肿瘤作用。

方法

我们使用A549细胞评估抗癌活性。研究了细胞活力、细胞周期、细胞凋亡及凋亡相关蛋白表达。

结果

HC中的活性化合物显著抑制A549细胞活力,并以浓度依赖的方式诱导A549细胞周期在S期或G2/M期积累,通过增加p21、p27、p53并降低细胞周期蛋白-E、-A、细胞周期蛋白依赖性激酶2(CDK2)、细胞周期蛋白依赖性激酶1(cdc-2,CDK1)蛋白表达诱导A549细胞停滞在S期或G2/M期。此外,HC通过上调半胱天冬酶-3、-8、Bax并降低Bcl-2蛋白表达诱导A549细胞晚期凋亡。

结论

马兜铃内酰胺BII、马兜铃内酰胺AII和去甲马兜铃二酮对人肺癌A549细胞的抗肿瘤作用是通过细胞周期阻滞和凋亡实现的。

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