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      Anti-Proliferative Effect and Phytochemical Analysis of Cymbopogon citratus Extract

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      1 , 2 , 2 , 3 , 4 , *
      BioMed Research International
      Hindawi Publishing Corporation

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          Abstract

          The antiproliferative and antioxidant potential of Cymbopogon citratus (Lemon grass) extracts were investigated. The extracts were isolated by solvent maceration method and thereafter subjected to antiproliferative activity test on five different cancer cells: human colon carcinoma (HCT-116), breast carcinoma (MCF-7 and MDA-MB 231), ovarian carcinoma (SKOV-3 and COAV), and a normal liver cell line (WRL 68). The cell viability was determined using MTT assay. The DPPH radical scavenging assay revealed a concentration dependent trend. A maximum percentage inhibition of 45% and an IC50 of 278  μ g/mL were observed when aqueous extract was evaluated. In contrast, 48.3% and IC50 of 258.9  μ g/mL were observed when 50% ethanolic extract was evaluated. Both extracts at concentration of 50 to 800  μ g/mL showed appreciative metal chelating activity with IC50 value of 172.2 ± 31  μ g/mL to 456.5 ± 30  μ g/mL. Depending on extraction solvent content, extract obtained from 50% ethanolic solvent proved to be more potent on breast cancer MCF-7 cell line (IC50 = 68  μ g/mL). On the other hand, 90% ethanolic extract showed a moderate potency on the ovarian cancer (COAV) and MCF-7 cells having an IC50 of 104.6  μ g/mL each. These results suggested antiproliferative efficacy of C. citratus ethanolic extract against human cancer cell lines.

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          Most cited references57

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          Anti-proliferative activity of essential oil extracted from Thai medicinal plants on KB and P388 cell lines.

          Anti-proliferative activity of essential oil from 17 Thai medicinal plants on human mouth epidermal carcinoma (KB) and murine leukemia (P388) cell lines using MTT assay were investigated. An amount of 1 x 10(4)cells/well of KB cell line and 1 x 10(5) cells/well of P388 cell line were treated with the oil samples at different concentrations ranging from 0.019 to 4.962 mg/ml. In KB cell line, Guava (Psidium guajava L.) leaf oil showed the highest anti-proliferative activity with the IC(50) value of 0.0379 mg/ml (4.37 times more potent than vincristine) whereas Sweet Basil (Ocimum basilicum L.) oil gave the highest anti-proliferative activity with the IC(50) value of 0.0362 mg/ml (12.7 times less potent than 5-FU) in P388 cell line. The results demonstrated the potential of essential oil from Thai medicinal plants for cancer treatment.
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            Gastric cytoprotection of the non-steroidal anti-inflammatory sesquiterpene, beta-caryophyllene.

            The gastric cytoprotective effect of beta-caryophyllene, an anti-inflammatory sesquiterpene, was investigated in rats. The oral administration of beta-caryophyllene to rats significantly inhibited gastric mucosal injuries induced by necrotizing agents such as absolute ethanol and 0.6 N HCl, although it failed to prevent water immersion stress- and indomethacin-induced gastric lesions. In addition, this compound hardly affected the secretion of gastric acid and pepsin. Thus, beta-caryophyllene elicited anti-inflammatory effects without any indication of gastric mucosal damage typical of non-steroidal anti-inflammatory agents. Furthermore, this compound manifested cytoprotective effects, rendering the two-dimensional efficacious beta-caryophyllene to be a clinically safe and potentially useful agent.
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              Citral is a new inducer of caspase-3 in tumor cell lines.

              Citral, 3,7-dimethyl-2,6-octadien-1-al, a key component of the lemon-scented essential oils extracted from several herbal plants such as lemon grass (Cymbopogon citratus), melissa (Melissa officinalis), verbena (Verbena officinalis) is used as a food additive and as a fragrance in cosmetics. In this study, we investigated the anti-cancer potential of citral and its mode of action. Concentrations of 44.5 muM, comparable to the concentration of citral in a cup of tea prepared from 1 g of lemon grass, induced apoptosis in several hematopoietic cancer cell lines. Apoptosis was accompanied by DNA fragmentation and caspase-3 catalytic activity induction. Citral activity (22.25 microM) was compared to a reference compound like staurosporine (0.7 microM), in respect to DNA fragmentation and caspase-3 enzymatic activity. The apoptotic effect of citral depended on the alpha,beta-unsaturated aldehyde group.
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                Author and article information

                Journal
                Biomed Res Int
                Biomed Res Int
                BMRI
                BioMed Research International
                Hindawi Publishing Corporation
                2314-6133
                2314-6141
                2014
                27 March 2014
                : 2014
                : 906239
                Affiliations
                1Department of Biomedical Sciences, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia
                2Al-Moalim Mohamed Awad Center for Scientific Miracles of Prophetic Medicine, College of Medicine, Taibah University, 3001 Madinah, Saudi Arabia
                3Department of Neurosurgery, College of Medicine, Taibah University, 3001 Madinah, Saudi Arabia
                4Faculty of Medicine, P.O. Box 30001, Al-Madinah Al-Munawarah, Saudi Arabia
                Author notes
                *Bassem Y. Sheikh: amohd2000@ 123456yahoo.com

                Academic Editor: Yih-Shou Hsieh

                Article
                10.1155/2014/906239
                3984801
                24791006
                777dc4a8-585c-4106-94e2-8ac4b81f1331
                Copyright © 2014 M. F. Halabi and B. Y. Sheikh.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 30 December 2013
                : 15 February 2014
                : 21 February 2014
                Funding
                Funded by: http://dx.doi.org/10.13039/501100002403 Taibah University
                Award ID: SMPM1434/A0102
                Categories
                Research Article

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