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      Antiproliferative Effects of Cynara cardunculus L. var. altilis (DC) Lipophilic Extracts

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          Abstract

          Besides being traditionally used to relieve hepatobiliary disorders, Cynara cardunculus L. has evidenced anticancer potential on triple-negative breast cancer (TNBC). This study highlights the antiproliferative effects of lipophilic extracts from C. cardunculus L. var. altilis (DC) leaves and florets, and of their major compounds, namely cynaropicrin and taraxasteryl acetate, against MDA-MB-231 cells. Our results demonstrated that MDA-MB-231 cells were much less resistant to leaves extract (IC 50 10.39 µg/mL) than to florets extract (IC 50 315.22 µg/mL), during 48 h. Moreover, leaves extract and cynaropicrin (IC 50 6.19 µg/mL) suppressed MDA-MB-231 cells colonies formation, via an anchorage-independent growth assay. Leaves extract and cynaropicrin were also assessed regarding their regulation on caspase-3 activity, by using a spectrophotometric assay, and expression levels of G2/mitosis checkpoint and Akt signaling pathway proteins, by Western blotting. Leaves extract increased caspase-3 activity, while cynaropicrin did not affect it. Additionally, they caused p21 Waf1/Cip1 upregulation, as well as cyclin B1 and phospho(Tyr15)-CDK1 accumulation, which may be related to G2 cell cycle arrest. They also downregulated phospho(Ser473)-Akt, without changing total Akt1 level. Cynaropicrin probably contributed to leaves extract antiproliferative action. These promising insights suggest that cultivated cardoon leaves lipophilic extract and cynaropicrin may be considered toward a natural-based therapeutic approach on TNBC.

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            Among cell cycle regulatory proteins that are activated following DNA damage, the cyclin-dependent kinase inhibitor p21(CDKN1A) plays essential roles in the DNA damage response, by inducing cell cycle arrest, direct inhibition of DNA replication, as well as by regulating fundamental processes, like apoptosis and transcription. These functions are performed through the ability of p21 to interact with a number of proteins involved in these processes. Despite an initial controversy, during the last years several lines of evidence have also indicated that p21 may be directly involved in DNA repair. In particular, the participation of p21 in nucleotide excision repair (NER), base excision repair (BER), and DNA translesion synthesis (TLS), has been suggested to occur thanks to its interaction with proliferating cell nuclear antigen (PCNA), a crucial protein involved in several aspects of DNA metabolism, and cell-cycle regulation. In this review, the multiple roles of p21 in the DNA damage response, including regulation of cell cycle, apoptosis and gene transcription, are discussed together with the most recent findings supporting the direct participation of p21 protein in DNA repair processes. In particular, spatio-temporal dynamics of p21 recruitment to sites of DNA damage will be considered together with several lines of evidence indicating a regulatory role for p21. In addition, the relevance of post-translational regulation in the fate (e.g. degradation) of p21 protein after cell exposure to DNA damaging agents will be analyzed. Both sets of evidence will be discussed in terms of the overall DNA damage response. 2010 Elsevier B.V. All rights reserved.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                MDPI
                1422-0067
                29 December 2016
                January 2017
                : 18
                : 1
                : 63
                Affiliations
                [1 ]Centro de Biotecnologia Agrícola e Agro-Alimentar do Alentejo (CEBAL)/Instituto Politécnico de Beja (IPBeja), 7801-908 Beja, Portugal; patricia.ramos@ 123456cebal.pt (P.A.B.R.); angela.guerra@ 123456cebal.pt (A.R.G.); olinda.guerreiro@ 123456cebal.pt (O.G.)
                [2 ]CICECO and Department of Chemistry, University of Aveiro, 3810-193 Aveiro, Portugal; santos.sonia@ 123456ua.pt (S.A.O.S.); cfreire@ 123456ua.pt (C.S.R.F.); armsil@ 123456ua.pt (A.J.D.S.)
                [3 ]CIISA, Centro de Investigação Interdisciplinar em Sanidade Animal, Faculdade de Medicina Veterinária, ULisboa, Avenida da Universidade Técnica, 1300-477 Lisboa, Portugal
                [4 ]CESAM and Department of Biology, University of Aveiro, 3810-193 Aveiro, Portugal; holiveira@ 123456ua.pt
                Author notes
                [* ]Correspondence: fatima.duarte@ 123456cebal.pt ; Tel.: +351-284-314-399
                Article
                ijms-18-00063
                10.3390/ijms18010063
                5297698
                28036090
                e3809082-c174-4d4f-b954-dd45e22c271c
                © 2016 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 (CC-BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 29 November 2016
                : 21 December 2016
                Categories
                Article

                Molecular biology
                cynara cardunculus l. var. altilis (dc),lipophilic extracts,cynaropicrin,taraxasteryl acetate,triple-negative breast cancer mda-mb-231 cell line,p21waf1/cip1 upregulation,phospho(tyr15)-cdk1 protein accumulation,phospho(ser473)-akt downregulation

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