Rodriguez-Hernandez 2018 Free Radic Biol Med

From Bioblast
Rodriguez-Hernández A, Staňková P, González R, De la Rosa AJ, Álamo-Martinez JM, Marin-Gómez LM, Sobotka O, Kučera O, Padillo FJ, Červinková Z, Muntané J (2018) The alteration of mitochondrial function is associated with the induction of endoplasmic reticulum stress autophagy and apoptosis by Sorafenib in liver cancer cells. Free Radic Biol Med.

Link: ScienceDirect

Rodriguez-Hernandez A, Stankova Pavla, Gonzalez R, De la Rosa AJ, Alamo-Martinez JM, Marin-Gomez LM, Sobotka Ondrej, Kucera Otto, Padillo FJ, Cervinkova Zuzana, Muntane Jordi (2018)

Event: Free Radic Biol Med

Sorafenib is the accepted molecular therapy for advanced hepatocarcinoma. Sorafenib reduced mitochondrial oxygen consumption, polarization and superoxide anion production in HepG2. These effects paralleled the induction of endoplasmic reticulum stress which was associated with Thr183JNK/JNK, Thr172AMPα, Thr308Akt/Akt and Thr32Foxo3a/Foxo3a increased ratios, as well as the reduction of Ser2481mTOR/mTOR and polysome profiling. This pattern was related to increased autophagy, and downregulation of Mcl-1 and Bcl-2 expression. The reduction of Thr308P-AKt/AKt and Ser473P-AKt/AKt ratios was associated with the progressive increase of CHOP and Bim expression. si-RNA and immunoprecipitation assays showed that Beclin-1 sequestration by Bim shifted autophagy to caspase-3-related apoptosis. Sorafenib appeared to be inactive in primary non-tumoral human hepatocytes. Sorafenib induced autophagy and apoptosis in xenograft mice model. In conclusion, the induction of mitochondrial dysfunction was associated with endoplasmic reticulum stress which was the driving mechanism involved in the sequential induction of autophagy and Bim-related apoptosis. Bim expression might also be related to the tight balance between AKt- and AMPK-related signaling in Foxo3a-dependent Bim upregulation.

Bioblast editor: Plangger M O2k-Network Lab: CZ Hradec Kralove Cervinkova Z

Labels: MiParea: Respiration, Pharmacology;toxicology  Pathology: Cancer 

Tissue;cell: Liver 

HRR: Oxygraph-2k 


Rodriguez-Hernández A(1), Staňková P(2,3), González R(1), De la Rosa AJ(1), Álamo-Martinez JM(1,4,5), Marin-Gómez LM(1,5), Sobotka O(2,3), Kučera O(2,3), Padillo FJ(1,4,5), Červinková Z(2,3), Muntané J(1,3,4,5)

  1. Inst Biomedicine Seville(IBIS), IBiS/Hospital Univ “Virgen del Rocío”/CSIC/Univ Seville, ES
  2. Dept Physiology, Fac Medicine, Charles Univ, Hradec Kralove, CZ
  3. COST-European Cooperation in Science & Technology. Mitoeagle Action number: CA15203
  4. Dept General Surgery, “Virgen del Rocío” Univ Hospital/IBiS/CSIC/Univ Seville
  5. Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas(CIBERehd); ES
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