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      Balibalosides, an Original Family of Glucosylated Sesterterpenes Produced by the Mediterranean Sponge Oscarella balibaloi

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          Abstract

          The chemical investigation of the recently described Mediterranean Homoscleromorpha sponge Oscarella balibaloi revealed an original family of five closely related glucosylated sesterterpenes 14, named balibalosides. Their structure elucidation was mainly inferred from NMR and HRMS data analyses. Balibalosides differ by the pattern of acetyl substitutions on the three sugar residues linked to the same aglycone sesterterpenoid core. From a biosynthetic perspective, these compounds may represent intermediates in the pathways leading to more complex sesterterpenes frequently found in Dictyoceratida, a sponge Order belonging to Demospongiae, a clade which is phylogenetically distinct from the Homoscleromorpha. While steroid and triterpenoid saponins were already well known from marine sponges, balibalosides are the first examples of glycosilated sesterterpenes.

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          Most cited references29

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          Feasibility of drug screening with panels of human tumor cell lines using a microculture tetrazolium assay.

          For the past 30 years strategies for the preclinical discovery and development of potential anticancer agents have been based largely upon the testing of agents in mice bearing transplantable leukemias and solid tumors derived from a limited number of murine as well as human sources. The feasibility of implementing an alternate approach, namely combined in vitro/in vivo screening for selective cytotoxicity among panels of human tumor cell lines derived from a broad spectrum of human solid tumors is under investigation. A group of 30 cell lines acquired from a variety of sources and representing 8 lung cancer pathologies as well as 76 cell lines representing 10 other categories of human cancer (carcinomas of colon, breast, kidney, prostate, ovary, head and neck; glioma; leukemia; melanoma; and sarcoma) have exhibited acceptable growth characteristics and suitable colorimetric profiles in a single, standard culture medium. Measurements of in vitro growth in microculture wells by cell-mediated reduction of tetrazolium showed excellent correlation (0.89 less than r2 less than 0.98) with measurements of cellular protein in adherent cell line cultures as well as viable cell count in suspension cell line cultures (0.94 less than r2 less than 0.99). Since the microculture tetrazolium assay provides sensitive and reproducible indices of growth as well as drug sensitivity in individual cell lines over the course of multiple passages and several months' cultivation, it appears suitable for initial-stage in vitro drug screening.
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            A tetrazolium-based colorimetric MTT assay to quantitate human monocyte mediated cytotoxicity against leukemic cells from cell lines and patients with acute myeloid leukemia.

            The MTT-colorimetric monocyte mediated cytotoxicity assay, based upon the ability of living cells to reduce 3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyltetrazolium bromide (MTT) into formazan, was evaluated using leukemic cells from five representative human leukemic cell lines and from 28 patients with acute myeloid leukemia (AML). An excellent linearity between absorbance and leukemic cell number was observed up to 5 x 10(4) cells/well and 50 x 10(4) cells/well for all cell lines and patients samples tested, respectively, in a 96-wells microtiter culture system. A huge variability in the susceptibility of leukemic cells to purified and IFN-gamma-activated human monocytes could be observed at effector-to-target cell (E:T) ratios of 1. The mean signal-to-noise ratio of the MTT assay for monocyte-leukemic cell mixtures from patients was 2.69 +/- 0.39 at E:T 1. In conclusion, the MTT based monocyte mediated cytotoxicity assay should be useful for studying the susceptibility of a variety of leukemic cells from cell lines and from patients with AML to monocytes in a rapid, sensitive and semi-automated manner.
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              Carbohydrate structural determination by NMR spectroscopy: modern methods and limitations.

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                Author and article information

                Journal
                Mar Drugs
                Mar Drugs
                marinedrugs
                Marine Drugs
                MDPI
                1660-3397
                06 May 2013
                May 2013
                : 11
                : 5
                : 1477-1489
                Affiliations
                [1 ]Nice Institute of Chemistry UMR 7272 CNRS—PCRE, University of Nice-Sophia Antipolis, Parc Valrose, 06108 Nice, France; E-Mails: coralie.audoin@ 123456unice.fr (C.A.); dominique.bonhomme@ 123456unice.fr (D.B.); julijana@ 123456scripps.edu (J.I.)
                [2 ]GREENSEA SAS, Promenade du Sergent Jean-Louis Navarro, 34140 Mèze, France; E-Mail: laurentrios@ 123456greentech.fr
                [3 ]Institut Méditerranéen de Biodiversité et d’Ecologie, Aix-Marseille University, UMR 7263 CNRS, Station Marine d’Endoume, 13007 Marseille, France; E-Mail: thierry.perez@ 123456imbe.fr
                [4 ]Fundación MEDINA, Centro de Excelencia en Investigación de Medicamentos Innovadores en Andalucía, Avda. Del Conocimiento, 3, Parque Tecnológico de Ciencias de la Salud, 18100 Armilla, Granada, Spain; E-Mails: mercedes.delacruz@ 123456medinaandalucia.es (M.C.); bastien.cautain@ 123456medinaandalucia.es (B.C.); mcandida.monteiro@ 123456medinaandalucia.es (M.C.M.); fernando.reyes@ 123456medinaandalucia.es (F.R.)
                Author notes
                [* ] Author to whom correspondence should be addressed; E-Mail: olivier.thomas@ 123456unice.fr ; Tel.: +33-492-076-134; Fax: +33-492-076-189.
                Article
                marinedrugs-11-01477
                10.3390/md11051477
                3707155
                23648552
                6cdb2d99-baa3-489e-9926-597376084681
                © 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
                : 25 March 2013
                : 09 April 2013
                : 22 April 2013
                Categories
                Article

                Pharmacology & Pharmaceutical medicine
                sponge,oscarella,homoscleromorpha,sesterterpenes,saponins
                Pharmacology & Pharmaceutical medicine
                sponge, oscarella, homoscleromorpha, sesterterpenes, saponins

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