Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/34816
English  |  正體中文  |  简体中文  |  Items with full text/Total items : 18240/20438 (89%)
Visitors : 5483975      Online Users : 997
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
    CNU IR > Offices > 456 >  Item 310902800/34816
    Please use this identifier to cite or link to this item: https://ir.cnu.edu.tw/handle/310902800/34816


    Title: The Inhibitory Effects and Cytotoxic Activities of the Stem Extract of Nepenthes miranda against Single-Stranded DNA-Binding Protein and Oral Carcinoma Cells
    Authors: Lin, En-Shyh
    Huang, Yen-Hua
    Chung, Jo-Chi
    Su, Hsin-Hui
    Huang, Cheng-Yang
    Contributors: Natl Taichung Univ Sci & Technol, Dept Beauty Sci
    Chung Shan Med Univ, Dept Biomed Sci
    Chia Nan Univ Pharm & Sci, Dept Pharm
    Chung Shan Med Univ Hosp, Dept Med Res
    Keywords: Nepenthes miranda
    SSB
    anticancer
    antipathogen
    Ca9-22 gingival carcinoma
    GC-MS analysis
    Sinningia bullata
    sitosterol
    plumbagin
    Date: 2023
    Issue Date: 2024-12-25 11:03:59 (UTC+8)
    Publisher: MDPI
    Abstract: The carnivorous pitcher plants of the genus Nepenthes exhibit many ethnobotanical uses, including treatments of stomachache and fever. In this study, we prepared different extracts from the pitcher, stem, and leaf extracts of Nepenthes miranda obtained using 100% methanol and analyzed their inhibitory effects on recombinant single-stranded DNA-binding protein (SSB) from Klebsiella pneumoniae (KpSSB). SSB is essential for DNA replication and cell survival and thus an attractive target for potential antipathogen chemotherapy. Different extracts prepared from Sinningia bullata, a tuberous member of the flowering plant family Gesneriaceae, were also used to investigate anti-KpSSB properties. Among these extracts, the stem extract of N. miranda exhibited the highest anti-KpSSB activity with an IC50 value of 15.0 +/- 1.8 mu g/mL. The cytotoxic effects of the stem extract of N. miranda on the survival and apoptosis of the cancer cell lines Ca9-22 gingival carcinoma, CAL27 oral adenosquamous carcinoma, PC-9 pulmonary adenocarcinoma, B16F10 melanoma, and 4T1 mammary carcinoma cells were also demonstrated and compared. Based on collective data, the cytotoxic activities of the stem extract at a concentration of 20 mu g/mL followed the order Ca9-22 > CAL27 > PC9 > 4T1 > B16F10 cells. The stem extract of N. miranda at a concentration of 40 mu g/mL completely inhibited Ca9-22 cell migration and proliferation. In addition, incubation with this extract at a concentration of 20 similar to mu g/mL boosted the distribution of the G2 phase from 7.9% to 29.2% in the Ca9-22 cells; in other words, the stem extract might suppress Ca9-22 cell proliferation by inducing G2 cell cycle arrest. Through gas chromatography-mass spectrometry, the 16 most abundant compounds in the stem extract of N. miranda were tentatively identified. The 10 most abundant compounds in the stem extract of N. miranda were used for docking analysis, and their docking scores were compared. The binding capacity of these compounds was in the order sitosterol > hexadecanoic acid > oleic acid > plumbagin > 2-ethyl-3-methylnaphtho[2,3-b]thiophene-4,9-dione > methyl alpha-D-galactopyranoside > 3-methoxycatechol > catechol > pyrogallol > hydroxyhydroquinone; thus, sitosterol might exhibit the greatest inhibitory capacity against KpSSB among the selected compounds. Overall, these results may indicate the pharmacological potential of N. miranda for further therapeutic applications.
    Relation: Plants-Basel, v.12, n.11, Article 2188
    Appears in Collections:[Offices] 456

    Files in This Item:

    File Description SizeFormat
    index.html0KbHTML5View/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