1. Metabolic implication of tigecycline as an efficacious second‐line treatment for sorafenib‐resistant hepatocellular carcinoma
- Author
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Helmut Pein, Alexander L. Gerbes, Johanna Pachmayr, Martin Müller, Martina Meßner, Simon Rothenfußer, Andreas Koeberle, Georg J. Arnold, Thomas Fröhlich, Angelika M. Vollmar, Alexandra K. Kiemer, Maximilian A. Ardelt, Sabine Schmitt, Carina Ortler, Lena Zobel, Petra Huber-Cantonati, Lars M. Koenig, and Hans Zischka
- Subjects
0301 basic medicine ,mitochondrial biogenesis ,Cell ,Apoptosis ,Mice, SCID ,Drug resistance ,Tigecycline ,Biochemistry ,antibiotics ,0302 clinical medicine ,Protein Synthesis Inhibitors ,Antibiotics ,Electron Acceptor Auxotrophy ,Mitochondrial Biogenesis ,Sorafenib Resistance ,Tumor Relapse ,tumor relapse ,Liver Neoplasms ,sorafenib resistance ,Sorafenib ,Mitochondria ,ddc ,medicine.anatomical_structure ,Hepatocellular carcinoma ,Female ,Biotechnology ,medicine.drug ,Carcinoma, Hepatocellular ,03 medical and health sciences ,Cell Line, Tumor ,Genetics ,medicine ,Animals ,Humans ,Adverse effect ,neoplasms ,Molecular Biology ,Cell Proliferation ,business.industry ,electron acceptor auxotrophy ,medicine.disease ,Xenograft Model Antitumor Assays ,digestive system diseases ,030104 developmental biology ,Mitochondrial biogenesis ,Drug Resistance, Neoplasm ,Cancer research ,Neoplasm Recurrence, Local ,business ,030217 neurology & neurosurgery ,Progressive disease - Abstract
Sorafenib represents the current standard of care for patients with advanced-stage hepatocellular carcinoma (HCC). However, acquired drug resistance occurs frequently during therapy and is accompanied by rapid tumor regrowth after sorafenib therapy termination. To identify the mechanism of this therapy-limiting growth resumption, we established robust sorafenib resistance HCC cell models that exhibited mitochondrial dysfunction and chemotherapeutic crossresistance. We found a rapid relapse of tumor cell proliferation after sorafenib withdrawal, which was caused by renewal of mitochondrial structures alongside a metabolic switch toward high electron transport system (ETS) activity. The translation-inhibiting antibiotic tigecycline impaired the biogenesis of mitochondrial DNA-encoded ETS subunits and limited the electron acceptor turnover required for glutamine oxidation. Thereby, tigecycline prevented the tumor relapse in vitro and in murine xenografts in vivo. These results offer a promising second-line therapeutic approach for advanced-stage HCC patients with progressive disease undergoing sorafenib therapy or treatment interruption due to severe adverse events.
- Published
- 2020
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