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Research Journal of Pharmacognosy، جلد ۹، شماره ۳، صفحات ۴۳-۴۹
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عنوان انگلیسی Network Analysis of 20S-Ginsenoside Rg3 Effect on Human Colorectal Adenocarcinoma Cell Line HT-29
چکیده انگلیسی مقاله Background and objectives: 20S-Ginsenoside Rg3 is a pharmacological active compound of ginseng. Evidences indicate that S20-Rg3 as an anti-cancer factor plays role in prevention and treatment of cancer. In the present study, proteomic data of 20S-ginsenoside Rg3 effect on human colorectal adenocarcinoma cell line HT-29 was analyzed via network analysis to understand more details about the molecular events. Methods: The differentially expressed proteins (DEPs) related to the effect of 20S-ginsenoside Rg3 on human colorectal adenocarcinoma cell line HT-29 were extracted from literature and analyzed via protein-protein interaction (PPI) network. The central nodes of the network were determined based on degree value and betweenness centrality. Results: Eight DEPS plus 100 added first neighbors were included in the PPI network. Five central nodes as hub-bottlenecks including ACTB, GAPDH, TP53, AKT1, and ALB among the added first neighbors and ANXA5 as hub-bottleneck and GSTP1 and PCNA as bottlenecks among the queried DEPs were introduced. Conclusion: PCNA, GSTP1, and ANxA5 as cell protective proteins are the crucial targeted proteins by 20S-ginsenoside Rg3 in the treated cell line HT-29. Up-regulation of GSTP1 and ANXA5 is correspondent to the cell protective property of 20S-ginsenoside Rg3, and down-regulation of PCNA refers to the opposite effect. It seems that cell protective roles of 20S-ginsenoside Rg3 are accompanied with the possible side effects.
کلیدواژه‌های انگلیسی مقاله Bioinformatics,differentially expressed proteins,Ginseng,Network analysis
نویسندگان مقاله Mona Zamanian Azodi |
Proteomics Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Babak Arjmand |
Cell Therapy and Regenerative Medicine Research Center, Endocrinology and Metabolism Molecular-Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.

Mostafa Rezaei Tavirani |
Proteomics Research Center, Faculty of Paramedical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Mahmood Khodadoost |
Department of Traditional Medicine, School of Traditional Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Mohammad Rostami Nejad |
Research Institute for Gastroenterology and Liver Diseases, Gastroenterology and Liver Diseases Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Nayebali Ahmadi |
Department of Traditional Medicine, School of Traditional Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

نشانی اینترنتی http://www.rjpharmacognosy.ir/article_151478_3ff031b150a6a020104eb0390568d571.pdf
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