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1.
Mar Drugs ; 13(7): 4470-91, 2015 Jul 20.
Article in English | MEDLINE | ID: mdl-26204945

ABSTRACT

Pancreatic cancer is one of the most aggressive cancer entities, with an extremely poor 5-year survival rate. Therefore, novel therapeutic agents with specific modes of action are urgently needed. Marine organisms represent a promising source to identify new pharmacologically active substances. Secondary metabolites derived from marine algae are of particular interest. The present work describes cellular and molecular mechanisms induced by an HPLC-fractionated, hydrophilic extract derived from the Baltic brown seaweed Fucus vesiculosus (Fv1). Treatment with Fv1 resulted in a strong inhibition of viability in various pancreatic cancer cell lines. This extract inhibited the cell cycle of proliferating cells due to the up-regulation of cell cycle inhibitors, shown on the mRNA (microarray data) and protein level. As a result, cells were dying in a caspase-independent manner. Experiments with non-dividing cells showed that proliferation is a prerequisite for the effectiveness of Fv1. Importantly, Fv1 showed low cytotoxic activity against non-malignant resting T cells and terminally differentiated cells like erythrocytes. Interestingly, accelerated killing effects were observed in combination with inhibitors of autophagy. Our in vitro data suggest that Fv1 may represent a promising new agent that deserves further development towards clinical application.


Subject(s)
Cell Cycle/drug effects , Cell Death/drug effects , Fucus/chemistry , Pancreatic Neoplasms/drug therapy , Plant Extracts/pharmacology , Autophagy/drug effects , Caspases/physiology , Cell Line, Tumor , Humans
2.
Science ; 296(5577): 2395-8, 2002 Jun 28.
Article in English | MEDLINE | ID: mdl-12089443

ABSTRACT

Phototaxis and photophobic responses of green algae are mediated by rhodopsins with microbial-type chromophores. We report a complementary DNA sequence in the green alga Chlamydomonas reinhardtii that encodes a microbial opsin-related protein, which we term Channelopsin-1. The hydrophobic core region of the protein shows homology to the light-activated proton pump bacteriorhodopsin. Expression of Channelopsin-1, or only the hydrophobic core, in Xenopus laevis oocytes in the presence of all-trans retinal produces a light-gated conductance that shows characteristics of a channel selectively permeable for protons. We suggest that Channelrhodopsins are involved in phototaxis of green algae.


Subject(s)
Chlamydomonas reinhardtii/metabolism , Ion Channels/chemistry , Ion Channels/metabolism , Light , Protons , Amino Acid Sequence , Animals , Bacteriorhodopsins/chemistry , Bacteriorhodopsins/metabolism , Butyric Acid/pharmacology , Chlamydomonas reinhardtii/chemistry , Chlamydomonas reinhardtii/genetics , Electric Conductivity , Hydrogen-Ion Concentration , Ion Channel Gating , Ion Channels/genetics , Ion Transport , Membrane Potentials , Molecular Sequence Data , Oocytes , Patch-Clamp Techniques , RNA, Complementary , Recombinant Proteins/metabolism , Retinaldehyde/pharmacology , Sequence Alignment , Temperature , Xenopus laevis
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