Literature DB >> 19016860

Marine toxins and the cytoskeleton: pectenotoxins, unusual macrolides that disrupt actin.

Begoña Espiña1, Juan A Rubiolo.   

Abstract

In recent years, many natural macrolactones have been found that display toxicity against the actin cytoskeleton. Pectenotoxins are macrolactones produced by species of the dinoflagellate genus Dinophysis. They were initially classified within the diarrheic shellfish poisoning group of toxins, because of their co-occurrence and biological origin, but mice toxicity assays demonstrated that pectenotoxins do not induce diarrheic symptoms. Intraperitoneal injection of pectenotoxins into mice produces high hepatotoxicity as the principal symptom, so the liver seems to be their target organ. Up to now, 15 pectenotoxin analogs have been discovered, with different toxicological potencies that are related to their structures. Now, it is generally accepted that the actin cytoskeleton is the principal molecular target of pectenotoxins. Although recent studies have demonstrated that pectenotoxins induce actin filament disruption by a capping effect, other kinds of activity, such as sequestration of actin, cannot be ruled out. All of the active analogs tested triggered disruption of the actin cytoskeleton and displayed potencies that correlated with their toxicity in mice. Moreover, pectenotoxins induce apoptosis to a higher degree in tumor cells than in normal cells of the same tissue. This fact opens the prospect of studying new chemotherapy agents and actin cytoskeleton dynamics with potential clinical applications.

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Year:  2008        PMID: 19016860     DOI: 10.1111/j.1742-4658.2008.06714.x

Source DB:  PubMed          Journal:  FEBS J        ISSN: 1742-464X            Impact factor:   5.542


  8 in total

1.  A convergent route to the CDEF-tetracycle of pectenotoxin-2.

Authors:  Daniel P Canterbury; Glenn C Micalizio
Journal:  Org Lett       Date:  2011-04-08       Impact factor: 6.005

2.  The methyl ester of okadaic acid is more potent than okadaic acid in disrupting the actin cytoskeleton and metabolism of primary cultured hepatocytes.

Authors:  Begoña Espiña; M Carmen Louzao; Eva Cagide; Amparo Alfonso; Mercedes R Vieytes; Takeshi Yasumoto; Luis M Botana
Journal:  Br J Pharmacol       Date:  2009-12-15       Impact factor: 8.739

Review 3.  Impact of marine drugs on cytoskeleton-mediated reproductive events.

Authors:  Francesco Silvestre; Elisabetta Tosti
Journal:  Mar Drugs       Date:  2010-03-25       Impact factor: 5.118

4.  Actin Crosslinking Toxins of Gram-Negative Bacteria.

Authors:  Karla J F Satchell
Journal:  Toxins (Basel)       Date:  2009-12-01       Impact factor: 4.546

Review 5.  Marine toxins: chemistry, toxicity, occurrence and detection, with special reference to the Dutch situation.

Authors:  Arjen Gerssen; Irene E Pol-Hofstad; Marnix Poelman; Patrick P J Mulder; Hester J van den Top; Jacob de Boer
Journal:  Toxins (Basel)       Date:  2010-04-23       Impact factor: 4.546

Review 6.  Solid Phase Adsorption Toxin Tracking (SPATT) Technology for the Monitoring of Aquatic Toxins: A Review.

Authors:  Mélanie Roué; Hélène Taiana Darius; Mireille Chinain
Journal:  Toxins (Basel)       Date:  2018-04-20       Impact factor: 4.546

Review 7.  Biotechnological and Pharmacological Applications of Biotoxins and Other Bioactive Molecules from Dinoflagellates.

Authors:  Joana Assunção; A Catarina Guedes; F Xavier Malcata
Journal:  Mar Drugs       Date:  2017-12-20       Impact factor: 5.118

Review 8.  Industrial Applications of Dinoflagellate Phycotoxins Based on Their Modes of Action: A Review.

Authors:  Kichul Cho; Jina Heo; Jinwook Han; Hyun Dae Hong; Hancheol Jeon; Hyun-Ju Hwang; Chang-Yu Hong; Daekyung Kim; Jong Won Han; Kyunghwa Baek
Journal:  Toxins (Basel)       Date:  2020-12-18       Impact factor: 4.546

  8 in total

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