Kristian M. Jacobsen,Nikolaj L. Villadsen,Thomas Tørring,Camilla Bak Nielsen,Trine Salomón,Morten Muhlig Nielsen,Michail Tsakos,Christian Sibbersen,Carsten Scavenius,Rikke Nielsen,Erik Christensen,Paula Fernández‐Guerra,Peter Bross,Jakob Skou Pedersen,Jan J. Enghild,Mogens Johannsen,Jørgen Frøkiær,Jens Overgaard,Michael R. Horsman,Morten Busk,Thomas B. Poulsen
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.