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Difference between revisions of "Torres-Quesada 2022 MitoFit Kinase"

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{{Publication
{{Publication
|title=Torres-Quesada O, Strich S, Stefan E (2022) Kinase perturbations redirect mitochondrial function. MitoFit Prep 2022.11. https://doi.org/10.26124/mitofit:2022-0011
|title=Torres-Quesada O, Strich S, Stefan E (2022) Kinase perturbations redirect mitochondrial function. https://doi.org/10.26124/mitofit:2022-0011 — ''2022-11-15 published in [https://doi.org//10.26124/bec:2022-0013 '''Bioenerg Commun 2022.13.''']''
|info= [[File:MitoFit Preprints pdf.png|left|160px|link=https://wiki.oroboros.at/images/9/91/Torres-Quesada_2022_MitoFit_Kinase.pdf|MitoFit pdf]] [https://wiki.oroboros.at/images/9/91/Torres-Quesada_2022_MitoFit_Kinase.pdf Kinase perturbations redirect mitochondrial function]<br/>  
|info=MitoFit Preprints 2022.11. [[File:MitoFit Preprints pdf.png|left|160px|link=https://wiki.oroboros.at/images/9/91/Torres-Quesada_2022_MitoFit_Kinase.pdf|MitoFit pdf]] [https://wiki.oroboros.at/images/9/91/Torres-Quesada_2022_MitoFit_Kinase.pdf Kinase perturbations redirect mitochondrial function] [[File:WatchThePresentationYoutube_icon.jpg|200px|link=https://www.youtube.com/watch?v=2--Bt1T7Zu0&t=1819s|»''Watch the presentation''«]]<br/>
|authors=Torres-Quesada Omar, Strich Sophie, Stefan Eduard
|authors=MitoFit Prep 2022.11.
|year=2022-04-11
|year=2022
|journal=MitoFit Prep
|journal=MitoFit Prep
|abstract=[[Torres-Quesada 2022 Abstract Bioblast]]: Protein kinases take the center stage in numerous signaling pathways by phosphorylating compartmentalized protein substrates for controlling cell proliferation, cell cycle and metabolism. Kinase dysfunctions have been linked to numerous human diseases such as cancer. This has led to the development of kinase inhibitors which aim to target oncogenic kinase activities. The specificity of the cancer blockers depends on the range of targeted kinases. Therefore, the question arises of how cell-type-specific off-target effects impair the specificities of cancer drugs. Blockade of kinase activities has been shown to converge on the energetic organelle, the mitochondria. In this review, we highlight examples of selected major kinases which impact mitochondrial signaling. Further, we discuss pharmacological strategies to target kinase activities which are linked to cancer progression and redirecting mitochondrial function. Finally, we propose that cell-based recordings of mitochondrial bioenergetic states might predict off-target or identify specific on-target effects of kinase inhibitors.
|abstract=[[Torres-Quesada 2022 Abstract Bioblast]]: Protein kinases take the center stage in numerous signaling pathways by phosphorylating compartmentalized protein substrates for controlling cell proliferation, cell cycle and metabolism. Kinase dysfunctions have been linked to numerous human diseases such as cancer. This has led to the development of kinase inhibitors which aim to target oncogenic kinase activities. The specificity of the cancer blockers depends on the range of targeted kinases. Therefore, the question arises of how cell-type-specific off-target effects impair the specificities of cancer drugs. Blockade of kinase activities has been shown to converge on the energetic organelle, the mitochondria. In this review, we highlight examples of selected major kinases which impact mitochondrial signaling. Further, we discuss pharmacological strategies to target kinase activities which are linked to cancer progression and redirecting mitochondrial function. Finally, we propose that cell-based recordings of mitochondrial bioenergetic states might predict off-target or identify specific on-target effects of kinase inhibitors.
 
|keywords=Kinases, signaling, mitochondria, kinase inhibitors, cancer, drug off-target effects
|keywords=Kinases, signaling, mitochondria, kinase inhibitors, cancer, drug off-target effects  
|editor=Doerrier C
|editor=Doerrier C
|mipnetlab=AT Innsbruck Oroboros
|mipnetlab=AT Innsbruck Oroboros
}}
}}
ORC'''ID''': [[File:ORCID.png|20px|link=https://orcid.org/0000-0003-3394-3075]] Torres-Quesada Omar,  
ORC'''ID''': [[File:ORCID.png|20px|link=https://orcid.org/0000-0003-3394-3075]] Torres-Quesada Omar,  
[[File:ORCID.png|20px|link=https://orcid.org/0000-0003-3650-4713]] Stefan Eduard
[[File:ORCID.png|20px|link=https://orcid.org/0000-0003-3650-4713]] Stefan Eduard

Latest revision as of 12:03, 8 January 2023

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Torres-Quesada 2022 MitoFit Kinase

Publications in the MiPMap
Torres-Quesada O, Strich S, Stefan E (2022) Kinase perturbations redirect mitochondrial function. https://doi.org/10.26124/mitofit:2022-00112022-11-15 published in Bioenerg Commun 2022.13.

» MitoFit Preprints 2022.11.

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Kinase perturbations redirect mitochondrial function »Watch the presentation«

MitoFit Prep 2022.11. (2022) MitoFit Prep

Abstract: Torres-Quesada 2022 Abstract Bioblast: Protein kinases take the center stage in numerous signaling pathways by phosphorylating compartmentalized protein substrates for controlling cell proliferation, cell cycle and metabolism. Kinase dysfunctions have been linked to numerous human diseases such as cancer. This has led to the development of kinase inhibitors which aim to target oncogenic kinase activities. The specificity of the cancer blockers depends on the range of targeted kinases. Therefore, the question arises of how cell-type-specific off-target effects impair the specificities of cancer drugs. Blockade of kinase activities has been shown to converge on the energetic organelle, the mitochondria. In this review, we highlight examples of selected major kinases which impact mitochondrial signaling. Further, we discuss pharmacological strategies to target kinase activities which are linked to cancer progression and redirecting mitochondrial function. Finally, we propose that cell-based recordings of mitochondrial bioenergetic states might predict off-target or identify specific on-target effects of kinase inhibitors. Keywords: Kinases, signaling, mitochondria, kinase inhibitors, cancer, drug off-target effects Bioblast editor: Doerrier C O2k-Network Lab: AT Innsbruck Oroboros

ORCID: ORCID.png Torres-Quesada Omar, ORCID.png Stefan Eduard


Labels: MiParea: Pharmacology;toxicology  Pathology: Cancer 

Organism: Human 





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