Research Article
    Pharmacognosy Reviews
    Vol. 12
    Issue 23
    2018
    pp. 94-102
    Open Access

    A Review: Melia azedarach L. as a Potent Anticancer Drug Martha Ervina1,2,

    Martha Ervina1,2,Sukardiman S3
    1Doctoral Program of Pharmaceutical Sciences, INDONESIA., 2Department of Pharmaceutical Biology, Faculty of Pharmacy, Widya Mandala Catholic University, Surabaya,, INDONESIA.
    3Department of Pharmacognosy and Phytochemistry, Faculty of Pharmacy, Airlangga University, Surabaya, INDONESIA.
    Correspondence:

    *Martha Ervina

    Doctoral Program of Pharmaceutical Sciences, INDONESIA.

    marthaervina@gmail.com

    Copyright:

    2018 Author(s)

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    Published:23/05/2018

    Abstract

    Chinaberry (Melia azedarach L., Meliaceae), a Mahogany family usually used as high quality timber, is native to Asia but now is found in other parts of tropical world continent. The leaves, fruits, bark, seed and root are use in traditional medicine and it has been shown to various pharmacological activities like antifungal, anti-malarial, antibacterial, hepatoprotective, anti-oxidant, anti-fertility, anthelmintic, antipyretic and cytotoxic. A review to its phytochemical and anticancer properties of M. azedarach and its sub species or varieties as an effort to analyze the literature on its developing used as anticancer agent. As results of literatures review indicates that fruit, bark, leaves, pulp and seed of Melia azedarach L. showed various in vitro cytotoxic activities in cancer cell lines, such as human colorectal carcinoma (HT-29), breast cancer (MCF-7, SK-BR-3), cervix hepatoma (HepG-2, SMMC-7721 and Hep3B), kidney epithelial cell (MDBK), human lung adenocarcinoma epithelial cell (A549), non-small cell lung cancer (H460), human lymphoblast lung (U937), human cancer promyelocytic leukemia (HL-60), AZ521 (stomach), human colon cancer (SW480), murine colorectal adenocarcinoma cell (CT26), human oral cancer cell (KB), human prostate cancer (PC3), liver (BEL7404), CNS (SH-SY5Y, U251, SF539), B16F10 mouse melanoma cell line; and showed various in vivo to adenocarsinoma mammary in C3H mice and mouse hepatocellular carcinoma H22 cells to BALB/c mice. Previous results suggested that cytotoxic organic compounds of Melia azedarach L. were supposed of flavonoids, triterpenoids (tirucallane), limonoids (meliarachin, meliatoxin B1, trichilin H, and toosendanin), steroids, and organic acids content compounds.

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    Keywords

    Anticancer
    cytotoxic
    Melia azedarach
    Melia
    triterpenoids
    limonoid
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