The potential of targeting lipid metabolizing cytochrome P450 enzymes for lung cancer treatment
- Date
- Nov 29, 2023
- Time
- 1:00 PM - 2:00 PM
- Speaker
- Simone Brixius-Anderko, Ph.D.
- Affiliation
- University of Pittsburgh School of Pharmacy, Center for Pharmacogenetics, Pittsburgh, USA
- Language
- en
- Main Topic
- Biologie
- Host
- Membrane Reconstitution Club / Theresia Gutmann
- Description
- Lung cancer is the leading cause for cancer-related deaths worldwide with limited treatment options. Thus, new orthogonal treatment options are urgently needed. The cytochrome P450 4F11 (CYP4F11) is heavily upregulated in lung cancer patients. CYP4F11 catalyzes the w-hydroxylation of arachidonic acid yielding 20-hydroxyeicosatetraenoic acid (20-HETE). 20-HETE is a potent lipid mediator and regulates blood pressure and angiogenesis in healthy individuals. In cancer, 20-HETE signaling leads to cell proliferation and migration and tumor angiogenesis. The Brixius lab has recently shown that a transient knockdown of CYP4F11 in lung cancer cell lines dramatically attenuates cell proliferation and migration, thus, demonstrating the high potential of CYP4F11 as drug target. We use a combination of cell biology, biochemistry, and X-ray protein crystallography to reveal structure and function of CYP4F11 and accelerate its use as lung cancer drug target for transformative therapeutics.
Last modified: Nov 30, 2023, 7:36:01 AM
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Max Planck Institute of Molecular Cell Biology and Genetics (CSBD SR Ground Floor)Pfotenhauerstraße10801307Dresden
- Phone
- +49 351 210-0
- Fax
- +49 351 210-2000
- MPI-CBG
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- http://www.mpi-cbg.de
Organizer
Max Planck Institute of Molecular Cell Biology and GeneticsPfotenhauerstraße10801307Dresden
- Phone
- +49 351 210-0
- Fax
- +49 351 210-2000
- MPI-CBG
- Homepage
- http://www.mpi-cbg.de
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