Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/34514
English  |  正體中文  |  简体中文  |  Items with full text/Total items : 18272/20499 (89%)
Visitors : 14432739      Online Users : 2619
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version
    Please use this identifier to cite or link to this item: https://ir.cnu.edu.tw/handle/310902800/34514


    Title: Enhancement of cytotoxicity and induction of apoptosis by cationic nano-liposome formulation of n-butylidenephthalide in breast cancer cells
    Authors: Huang, Xiao-Fan
    Chang, Kai-Fu
    Lin, Yu-Ling
    Liao, Kuang-Wen
    Hsiao, Chih-Yen
    Sheu, Gwo-Tarng
    Tsai, Nu-Man
    Contributors: Chung Shan Med Univ, Inst Med
    Chung Shan Med Univ, Dept Med Lab & Biotechnol
    Acad Sinica, Agr Biotechnol Res Ctr
    Natl Chiao Tung Univ, Dept Biol Sci & Technol
    Natl Chiao Tung Univ, Inst Mol Med & Bioengn
    Ditmanson Med Fdn Chia Yi Christian Hosp, Div Nephrol, Dept Internal Med
    Chia Nan Univ Pharm & Sci, Dept Hosp & Hlth Care Adm
    Chung Shan Med Univ Hosp, Clin Lab
    Keywords: Polycationic liposome containing PEI and polyethylene glycol complex (LPPC)
    n-Butylidenephthalide (BP)
    Cell apoptosis
    Cell cycle
    Synergistic effect
    Date: 2021
    Issue Date: 2023-11-11 12:00:21 (UTC+8)
    Publisher: IVYSPRING INT PUBL
    Abstract: Breast cancer is the second most common malignancy in women. Current clinical therapy for breast cancer has many disadvantages, including metastasis, recurrence, and poor quality of life. Furthermore, it is necessary to find a new therapeutic drug for breast cancer patients to meet clinical demand. n-Butylidenephthalide (BP) is a natural and hydrophobic compound that can inhibit several tumors. However, BP is unstable in aqueous or protein-rich environments, which reduces the activity of BP. Therefore, we used an LPPC (Lipo-PEG-PEI complex) that can encapsulate both hydrophobic and hydrophilic compounds to improve the limitation of BP. The purpose of this study is to investigate the anti-tumor mechanisms of BP and BP/LPPC and further test the efficacy of BP encapsulated by LPPC on SK-BR-3 cells. BP inhibited breast cancer cell growth, and LPPC encapsulation (BP/LPPC complex) enhanced the cytotoxicity on breast cancer by stabilizing the BP activity and offering endocytic pathways. Additionally, BP and LPPC-encapsulated BP induced cell cycle arrest at the G0/G1 phase and might trigger both extrinsic as well as intrinsic cell apoptosis pathway, resulting in cell death. Moreover, the BP/LPPC complex had a synergistic effect with doxorubicin of enhancing the inhibitory effect on breast cancer cells. Consequently, LPPC-encapsulated BP could improve the anti-cancer effects on breast cancer in vitro. In conclusion, BP exhibited an anti-cancer effect on breast cancer cells, and LPPC encapsulation efficiently improved the cytotoxicity of BP via an acceleration of entrapment efficiency to induce cell cycle block and apoptosis. Furthermore, BP/LPPC exhibited a synergistic effect in combination with doxorubicin.
    Relation: INT J MED SCI, v.18, n.13, pp.2930-2942
    Appears in Collections:[Dept. of Hospital and Health (including master's program)] Periodical Articles

    Files in This Item:

    File Description SizeFormat
    ijms.51439.pdf2458KbAdobe PDF137View/Open
    index.html0KbHTML445View/Open


    All items in CNU IR are protected by copyright, with all rights reserved.


    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback