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      Lee et al., Inhibitory Effect and Mechanism of Antiproliferation of Isoatriplicolide Tiglate (PCAC) from Paulownia Coreana. Molecules 2012, 17, 5945-5951: A Note Regarding Paulownia coreana.

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          Abstract

          I read with interest the article by Lee et al. entitled “Inhibitory Effect and Mechanism of Antiproliferation of Isoatriplicolide Tiglate (PCAC) from Paulownia Coreana” [1]. This article is quite interesting and the authors should be complimented for the significant amount of work they have done. The purpose of this letter is to call attention to the need for some clarification on the name of the plant described in this article. Lee et al. state: “Paulownia coreana has traditionally been used as the medicine and health food in the treatment of cancer and infectious diseases.” and elsewhere: “In fact, many cancer research studies have been conducted using traditional medicinal plants such as P. coreana.” [1]. I have been studying the pharmacotoxicological properties of the medicinal plants of Asia and the Pacific for the last 15 years [2,3,4,5,6,7] and the sole members of the genus Paulownia Siebold & Zucc. (1835) officially recognized in China and Korea are Paulownia catalpifolia T. Gong ex D.Y. Hong, Paulownia elongata S.Y. Hu, Paulownia fargesii Franch., Paulownia fortunei (Seem.) Hemsl., Paulownia kawakamii T. Itô, Paulownia taiwaniana T.W. Hu & H.J. Chang and Paulownia tomentosa (Thunb.) Steud. [8]. Paulownia coreana does not exist and therefore cannot be medicinal nor the source of the phytochemical described in [1]. In addition, the chemical structure of isoatriplicolide tiglate as provided by Lee et al. is incomplete as regards to carbon numbering and the class of sesquiterpene to which this molecule belongs is not specified. Prompt revision of the name assigned to this plant (and henceforth any comments on its properties or phytochemical content) is required to ensure the accuracy of the scientific record.

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          Inhibitory Effect and Mechanism on Antiproliferation of Isoatriplicolide Tiglate (PCAC) from Paulownia Coreana

          Paulownia coreana has traditionally been used as the medicine and health food in the treatment of cancer and infectious diseases. In the present study, a new antiproliferation agent, isoatriplicolide tiglate (PCAC) was isolated from the chloroform soluble fraction of the leaves of Paulownia coreana. The antiproliferation activities of PCAC plant extract was examined in breast and cervical cancer cell lines in a time-and dose-dependent manners. Our in vitro experiments showed that PCAC suppresses the cell growth and proliferation of cancer cells at a relatively low concentration ( 50 µg/mL). Western blot analysis showed that concentration higher than 50 µg/mL induces a time-dependent increase in the percentage of apoptotic cells. In this case, PCAC uses both extrinsic and intrinsic pathways for the apoptosis. PCAC treatment decreased the expression of pro-caspase 8, 9, and 3, the main regulators of apoptotic cell death, in MDA-MB-231 cells, accompanied by the activation of caspase 8, 9, and 3. More importantly, PCAC inhibited the in vitro proliferation of six other human breast and cervical cancer cell lines. In conclusion, our data strongly suggest that PCAC acts as an antiproliferation agents particularly against breast and cervical cancers by inducing cell cycle arrest in the S/G2 phase and caspase dependent apoptosis at relatively low ( 50 µg/mL) concentrations, respectively.
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            Author and article information

            Journal
            Molecules
            Molecules
            molecules
            Molecules
            MDPI
            1420-3049
            26 February 2013
            March 2013
            : 18
            : 3
            : 2587-2588
            Affiliations
            School of Biomedical Sciences, University of Nottingham, Medical School, Queen’s Medical Centre, Nottingham NG7 2UH, UK; E-Mail: Christophe.Wiart@ 123456nottingham.edu.my
            Article
            molecules-18-02587
            10.3390/molecules18032587
            6269675
            23442934
            254c95c4-141a-4ea6-8e31-fa47662a56be
            © 2013 by the authors; licensee MDPI, Basel, Switzerland.

            This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license ( http://creativecommons.org/licenses/by/3.0/).

            History
            : 18 February 2013
            : 22 February 2013
            : 22 February 2013
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