| Literature DB >> 30122371 |
Kristian Mark Jacobsen1, Nikolaj Lilholm Villadsen1, Thomas Tørring2, Camilla Bak Nielsen3, Trine Salomón3, Morten Muhlig Nielsen4, Michail Tsakos1, Christian Sibbersen3, Carsten Scavenius5, Rikke Nielsen6, Erik Ilsø Christensen6, Paula Fernandez Guerra7, Peter Bross7, Jakob Skou Pedersen8, Jan Johannes Enghild9, Mogens Johannsen3, Jørgen Frøkiær10, Jens Overgaard11, Michael R Horsman11, Morten Busk11, Thomas B Poulsen12.
Abstract
The natural product family of macrocyclic lipodepsipeptides containing the 4-amido-2,4-pentadienoate functionality possesses intriguing cytotoxic selectivity toward hypoxic cancer cells. These subpopulations of cancer cells display increased metastatic potential and resistance to chemo- and radiotherapy. In this paper, we present studies on the mechanism of action of these natural products in hypoxic cancer cells and show that this involves rapid and hypoxia-selective collapse of mitochondrial integrity and function. These events drive a regulated cell death process that potentially could function as a powerful tool in the fight against chemo- and radiotherapy-resistant cancer cells. Toward that end, we demonstrate activity in two different mouse tumor models.Entities:
Keywords: ROS; cell death; mitochondria; mode of action; natural products; tumor hypoxia
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Year: 2018 PMID: 30122371 DOI: 10.1016/j.chembiol.2018.07.010
Source DB: PubMed Journal: Cell Chem Biol ISSN: 2451-9448 Impact factor: 8.116