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      7-Epiclusianone, a Benzophenone Extracted from Garcinia brasiliensis ( Clusiaceae), Induces Cell Cycle Arrest in G1/S Transition in A549 Cells

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          Abstract

          Lung cancer is the leading cause of cancer deaths in the world. Disease stage is the most relevant factor influencing mortality. Unfortunately, most patients are still diagnosed at an advanced stage and their five-year survival rate is only 4%. Thus, it is relevant to identify novel drugs that can improve the treatment options for lung cancer. Natural products have been an important source for the discovery of new compounds with pharmacological potential including antineoplastic agents. We have previously isolated a prenylated benzophenone (7-epiclusianone) from Garcinia brasiliensis ( Clusiaceae) that has several biological properties including antiproliferative activity against cancer cell lines. In continuation with our studies, the present work aimed to investigate the mechanisms involved with antiproliferative activity of 7-epiclusianone in A549 cells. Our data showed that 7-epiclusianone reduced the viability of A549 cells in a concentration-dependent manner (IC 50 of 16.13 ± 1.12 μM). Cells were arrested in G1/S transition and apoptosis was induced. In addition, we observed morphological changes with cytoskeleton disorganization in consequence of the treatment. Taken together, the results showed that cell cycle arrest in G1/S transition is the main mechanism involved with antiproliferative activity of 7-epiclusianone. Our results are promising and open up the prospect of using this compound in further anticancer in vivo studies.

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          A chemical method for fast and sensitive detection of DNA synthesis in vivo.

          We have developed a method to detect DNA synthesis in proliferating cells, based on the incorporation of 5-ethynyl-2'-deoxyuridine (EdU) and its subsequent detection by a fluorescent azide through a Cu(I)-catalyzed [3 + 2] cycloaddition reaction ("click" chemistry). Detection of the EdU label is highly sensitive and can be accomplished in minutes. The small size of the fluorescent azides used for detection results in a high degree of specimen penetration, allowing the staining of whole-mount preparations of large tissue and organ explants. In contrast to BrdU, the method does not require sample fixation or DNA denaturation and permits good structural preservation. We demonstrate the use of the method in cultured cells and in the intestine and brain of whole animals.
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            DNA damage checkpoints: from initiation to recovery or adaptation.

            In response to diverse genotoxic stresses, cells activate DNA damage checkpoint pathways to protect genomic integrity and promote survival of the organism. Depending on DNA lesions and context, damaged cells with alarmed checkpoints can be eliminated by apoptosis or silenced by cellular senescence, or can survive and resume cell cycle progression upon checkpoint termination. Over the past two years a plethora of mechanistic studies have provided exciting insights into the biology and pathology of checkpoint initiation and signal propagation, and have revealed the various ways in which the response can be terminated: through recovery, adaptation or cancer-prone subversion. Such studies highlight the dynamic nature of these processes and help us to better understand the molecular basis, spatiotemporal orchestration and biological significance of the DNA damage response in normal and cancerous cells.
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              Drugs that target dynamic microtubules: a new molecular perspective.

              Microtubules have long been considered an ideal target for anticancer drugs because of the essential role they play in mitosis, forming the dynamic spindle apparatus. As such, there is a wide variety of compounds currently in clinical use and in development that act as antimitotic agents by altering microtubule dynamics. Although these diverse molecules are known to affect microtubule dynamics upon binding to one of the three established drug domains (taxane, vinca alkaloid, or colchicine site), the exact mechanism by which each drug works is still an area of intense speculation and research. In this study, we review the effects of microtubule-binding chemotherapeutic agents from a new perspective, considering how their mode of binding induces conformational changes and alters biological function relative to the molecular vectors of microtubule assembly or disassembly. These "biological vectors" can thus be used as a spatiotemporal context to describe molecular mechanisms by which microtubule-targeting drugs work. © 2011 Wiley Periodicals, Inc.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Molecules
                Molecules
                molecules
                Molecules
                MDPI
                1420-3049
                15 July 2015
                July 2015
                : 20
                : 7
                : 12804-12816
                Affiliations
                [1 ]Institute of Biomedical Sciences, Federal University of Alfenas, 37130-000 Alfenas, Brazil; E-Mail: alfer_gui@ 123456hotmail.com
                [2 ]Department of Cell and Developmental Biology, Institute of Biomedical Sciences, University of Sao Paulo, 05508-000 São Paulo, Brazil; E-Mails: eloniero@ 123456yahoo.com (E.L.N.); adam.arai@ 123456gmail.com (A.A.M.); glaucia.usp@ 123456gmail.com (G.M.M.-S.)
                [3 ]Institute of Chemistry, Federal University of Alfenas, 37130-000 Alfenas, Brazil; E-Mails: edm_quimica@ 123456yahoo.com.br (E.D.C.); welton_rosa@ 123456hotmail.com (W.R.); marisigs@ 123456gmail.com (M.G.S.)
                [4 ]Institute of Environmental, Chemical and Pharmaceutical Sciences, Federal University of Sao Paulo, 09920-000 Diadema, Brazil; E-Mail: joao.lago@ 123456unifesp.br
                [5 ]Institute of Chemistry, Federal University of Viçosa, 36570-900 Viçosa, Brazil; E-Mail: marcelo_hs@ 123456yahoo.com.br
                Author notes
                [* ]Author to whom correspondence should be addressed; E-Mail: marisaionta@ 123456gmail.com ; Tel.: +55-35-3299-1309.
                Article
                molecules-20-12804
                10.3390/molecules200712804
                6332126
                26184153
                057f19d7-8a6c-4d3d-9ebd-7188bbc29cfe
                © 2015 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/4.0/).

                History
                : 16 May 2015
                : 08 July 2015
                Categories
                Article

                7-epiclusianone,garcinia brasiliensis,antiproliferative activity,lung cancer,cell cycle arrest,cell death

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