An in vivo molecular response analysis of colorectal cancer treated with Astragalus membranaceus extract

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題名:	An in vivo molecular response analysis of colorectal cancer treated with Astragalus membranaceus extract
作者:	蘇立仁;TSENG, AILUN;YANG, CHIH-HSUEH;CHEN, CHIH-HAO;CHEN, CHANG-HAN;HSU, SHIH-LAN;LEE, MEI-HSIEN;LEE, HOONG-CHIEN;SU, LI-JEN
貢獻者:	生醫理工學院生醫科學與工程學系
關鍵詞:	Animals;Antineoplastic Agents, Phytogenic - pharmacology;Astragalus (Plants);Astragalus membranaceus;Biomarkers;Cancer therapies;Care and treatment;Colorectal cancer;Colorectal Neoplasms - pathology;Drugs;Drugs, Chinese Herbal - pharmacology;Gene expression;HCT116 Cells;Health aspects;Humans;Laboratories;Male;Materia medica, Vegetable;Medicine, Chinese Traditional;Mice;Mice, Nude;microarray;microRNA;Oligonucleotide Array Sequence Analysis;Plant extracts;Real-Time Polymerase Chain Reaction;Studies;Transcriptome - drug effects;Tumors;xenograft;Xenograft Model Antitumor Assays
日期:	2016-02-01
上傳時間:	2026-04-23 11:15:00 (UTC+8)
出版者:	Spandidos Publications;Greece: D.A. Spandidos
摘要:	摘要： The fact that many chemotherapeutic drugs cause chemoresistance and side effects during the course of colorectal cancer treatment necessitates development of novel cytotoxic agents aiming to attenuate new molecular targets. Here, we show that Astragalus membranaceus (Fischer) Bge. var. mongolicus (Bge.) Hsiao (AM), a traditional Chinese medicine, can inhibit tumor growth in vivo and elucidate the underlying molecular mechanisms. The antitumor effect of AM was assessed on the subcutaneous tumors of human colorectal cancer cell line HCT116 grafted into nude mice. The mice were treated with either water or 500 mg/kg AM once per day, before being sacrificed for extraction of tumors, which were then subjected to microarray expression profiling. The gene expression of the extraction was then profiled using microarray analysis. The identified genes differentially expressed between treated mice and controls reveal that administration of AM suppresses chromosome organization, histone modification, and regulation of macromolecule metabolic process. A separate analysis focused on differentially expressed microRNAs revealing involvement of macromolecule metabolism, and intracellular transport, as well as several cancer signaling pathways. For validation, the input of the identified genes to The Library of Integrated Network-based Cellular Signatures led to many chemopreventive agents of natural origin that produce similar gene expression profiles to that of AM. The demonstrated effectiveness of AM suggests a potential therapeutic drug for colorectal cancer. 其他題名： Oncol Rep 出版者： Greece: D.A. Spandidos 出版日期： 2016-02-01 出處： Oncology reports, 2016-02, Vol.35 (2), p.659-668 版權： Copyright: © Tseng et al. 版權： COPYRIGHT 2016 Spandidos Publications 版權： Copyright Spandidos Publications UK Ltd. 2016 版權： Copyright: © Tseng et al. 2016 識別號： ISSN: 1021-335X 識別號： ISSN: 1791-2431 識別號： EISSN: 1791-2431 識別號： DOI: 10.3892/or.2015.4441 識別號： PMID: 26719057
顯示於類別:	[生醫科學與工程學系] 期刊論文

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