Literature DB >> 33567702

Anemonia sulcata and Its Symbiont Symbiodinium as a Source of Anti-Tumor and Anti-Oxoxidant Compounds for Colon Cancer Therapy: A Preliminary in Vitro Study.

Laura Cabeza1,2,3, Mercedes Peña1,2,3, Rosario Martínez4, Cristina Mesas1,2,3, Milagros Galisteo5, Gloria Perazzoli1,2,3, Jose Prados1,2,3, Jesús M Porres4, Consolación Melguizo1,2,3.   

Abstract

Recently, invertebrate marine species have been investigated for the presence of natural products with antitumor activity. We analyzed the invertebrate Anemonia sulcata with (W) and without (W/O) the presence of its microalgal symbiont Symbiodinium as a source of bioactive compounds that may be applied in the therapy and/or prevention of colorectal cancer (CRC). Animals were mechanically homogenized and subjected to ethanolic extraction. The proximate composition and fatty acid profile were determined. In addition, an in vitro digestion was performed to study the potentially dialyzable fraction. The antioxidant and antitumor activity of the samples and the digestion products were analyzed in CRC cells in vitro. Our results show a high concentration of polyunsaturated fatty acid in the anemone and a great antioxidant capacity, which demonstrated the ability to prevent cell death and a high antitumor activity of the crude homogenates against CRC cells and multicellular tumor spheroids, especially W/O symbiont. These preliminary results support that Anemonia sulcata could be a source of bioactive compounds with antioxidant and antitumor potential against CRC and that the absence of its symbiont may enhance these properties. Further studies will be necessary to define the bioactive compounds of Anemonia sulcata and their mechanisms of action.

Entities:  

Keywords:  Anemonia sulcata; Symbiodinium; antioxidant activity; antitumor activity; colorectal cancer

Year:  2021        PMID: 33567702      PMCID: PMC7915377          DOI: 10.3390/biology10020134

Source DB:  PubMed          Journal:  Biology (Basel)        ISSN: 2079-7737


  61 in total

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