Andrographolide Inhibits Proliferation of Colon Cancer SW-480 Cells via Downregulating Notch Signaling Pathway

被引:16
|
作者
Khan, Imran [1 ,2 ]
Mahfooz, Sadaf [1 ,2 ]
Saeed, Mohd [3 ]
Ahmad, Irfan [4 ,5 ]
Ansari, Irfan A. [2 ]
机构
[1] BezmialemVakif Univ, Beykoz Inst Life Sci & Biotechnol, Dept Mol Biol, Istanbul, Turkey
[2] Integral Univ, Dept Biosci, Kursi Rd, Lucknow 226026, Uttar Pradesh, India
[3] Univ Hail, Dept Biol, Coll Sci, Hail, Saudi Arabia
[4] King Khalid Univ, Dept Clin Lab Sci, Coll Appl Med Sci, Abha, Saudi Arabia
[5] King Khalid Univ, Res Ctr Adv Mat Sci, Abha, Saudi Arabia
关键词
Andrographis; cell cytotoxicity; apoptosis; cell cycle; flow cytometry; NOTCH-1; JAGGED-1; gene expression;
D O I
10.2174/1871520620666200717143109
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Recently, the Notch signaling pathway has gained attention as a potential therapeutic target for chemotherapeutic intervention. However, the efficacy of previously known Notch inhibitors in colon cancer is still unclear. The purpose of this study was to investigate the effect of andrographolide on aberrantly activated Notch signaling in SW-480 cells in vitro. Methods: The cytostatic potential of andrographolide on SW-480 cells was evaluated by 3-(4,5-dimethylthiazol2-yl)-2, 5-diphenyl tetrazolium bromide (MTT) assay, morphology assessment, and colony formation assay. The apoptotic activity was evaluated by FITC Annexin V assay, 4',6-diamidino-2-phenylindole (DAPI), Hoechst, Rhodamine 123, and Mito Tracker CMXRos staining. Scratch assay was conducted for migratory potential assessment. 7'-Dichlorodihydrofluorescein Diacetate (DCFH-DA) staining was used to evaluate the Reactive Oxygen Species (ROS) generation. Relative mRNA expression of Bax, Bcl2, NOTCH 1, and JAGGED 1 was estimated by Real-Time Quantitative Reverse Transcription PCR (qRT-PCR). Cell cycle phase distribution was evaluated by Annexin V-FITC/PI staining. Results: MTT assay demonstrated the dose and time-dependent cytotoxicity of andrographolide on SW-480 cells. It also inhibited the migratory and colony forming potential of SW-480 cells. Furthermore, andrographolide also showed disruption of mitochondrial membrane potential and induced apoptosis through nuclear condensation. Flow cytometric evaluation showed that andrographolide enhanced early and late apoptotic cells and induced upregulation of pro-apoptotic (Bax and Bad) and downregulation of anti-apoptotic Bcl2 in treated SW480 cells. Andrographolide augmented intracellular ROS generation and induced G(0)/G(1) phase cell cycle arrest in colon cancer SW-480 cells. Furthermore, andrographolide repressed the Notch signaling by decreasing the expression of NOTCH 1 and JAGGED 1. Conclusion: The findings suggested that andrographolide constraint the growth of SW-480 cells through the inhibition of the Notch signaling pathway.
引用
收藏
页码:487 / 497
页数:11
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