Translational implications of targeting annexin A2: From membrane repair to muscular dystrophy, cardiovascular disease and cancer

Abstract Background Annexin A2 contributes to several key cellular functions and processes, including membrane repair. Effective repair prevents cell death and degeneration, especially in skeletal or cardiac muscle, epithelia, and endothelial cells. To maintain cell integrity after damage, mammalian...

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Main Authors: Victor G. Kayejo, Hannah Fellner, Roshan Thapa, Peter A. Keyel
Format: Article
Language:English
Published: Wiley 2023-10-01
Series:Clinical and Translational Discovery
Subjects:
Online Access:https://doi.org/10.1002/ctd2.240
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author Victor G. Kayejo
Hannah Fellner
Roshan Thapa
Peter A. Keyel
author_facet Victor G. Kayejo
Hannah Fellner
Roshan Thapa
Peter A. Keyel
author_sort Victor G. Kayejo
collection DOAJ
description Abstract Background Annexin A2 contributes to several key cellular functions and processes, including membrane repair. Effective repair prevents cell death and degeneration, especially in skeletal or cardiac muscle, epithelia, and endothelial cells. To maintain cell integrity after damage, mammalian cells activate multiple membrane repair mechanisms. One protein family that facilitates membrane repair processes are the Ca2+‐regulated phospholipid‐binding annexins. Body Annexin A2 facilitates repair in association with S100A10 and related S100 proteins by forming a plug and linking repair to other physiologic functions. Deficiency of annexin A2 enhances cellular degeneration, exacerbating muscular dystrophy and degeneration. Downstream of repair, annexin A2 links the membrane with the cytoskeleton, calcium‐dependent endocytosis, exocytosis, cell proliferation, transcription, and apoptosis to extracellular roles, including vascular fibrinolysis, and angiogenesis. These roles regulate cardiovascular disease progression. Finally, annexin A2 protects cancer cells from membrane damage due to immune cells or chemotherapy. Since these functions are regulated by post‐translational modifications, they represent a therapeutic target for reducing the negative consequences of annexin A2 expression. Conclusion Thus, connecting the roles of annexin A2 in repair to its other physiologic functions represents a new translational approach to treating muscular dystrophy and cardiovascular diseases without enhancing its pro‐tumorigenic activities.
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spelling doaj.art-10c72f45c45e40e99a3715c4d48a62752023-10-27T11:42:29ZengWileyClinical and Translational Discovery2768-06222023-10-0135n/an/a10.1002/ctd2.240Translational implications of targeting annexin A2: From membrane repair to muscular dystrophy, cardiovascular disease and cancerVictor G. Kayejo0Hannah Fellner1Roshan Thapa2Peter A. Keyel3Department of Biological Sciences Texas Tech University Lubbock Texas USADepartment of Biological Sciences Texas Tech University Lubbock Texas USADepartment of Biological Sciences Texas Tech University Lubbock Texas USADepartment of Biological Sciences Texas Tech University Lubbock Texas USAAbstract Background Annexin A2 contributes to several key cellular functions and processes, including membrane repair. Effective repair prevents cell death and degeneration, especially in skeletal or cardiac muscle, epithelia, and endothelial cells. To maintain cell integrity after damage, mammalian cells activate multiple membrane repair mechanisms. One protein family that facilitates membrane repair processes are the Ca2+‐regulated phospholipid‐binding annexins. Body Annexin A2 facilitates repair in association with S100A10 and related S100 proteins by forming a plug and linking repair to other physiologic functions. Deficiency of annexin A2 enhances cellular degeneration, exacerbating muscular dystrophy and degeneration. Downstream of repair, annexin A2 links the membrane with the cytoskeleton, calcium‐dependent endocytosis, exocytosis, cell proliferation, transcription, and apoptosis to extracellular roles, including vascular fibrinolysis, and angiogenesis. These roles regulate cardiovascular disease progression. Finally, annexin A2 protects cancer cells from membrane damage due to immune cells or chemotherapy. Since these functions are regulated by post‐translational modifications, they represent a therapeutic target for reducing the negative consequences of annexin A2 expression. Conclusion Thus, connecting the roles of annexin A2 in repair to its other physiologic functions represents a new translational approach to treating muscular dystrophy and cardiovascular diseases without enhancing its pro‐tumorigenic activities.https://doi.org/10.1002/ctd2.240annexincancercardiovascular diseasemembrane repairmuscular dystrophy
spellingShingle Victor G. Kayejo
Hannah Fellner
Roshan Thapa
Peter A. Keyel
Translational implications of targeting annexin A2: From membrane repair to muscular dystrophy, cardiovascular disease and cancer
Clinical and Translational Discovery
annexin
cancer
cardiovascular disease
membrane repair
muscular dystrophy
title Translational implications of targeting annexin A2: From membrane repair to muscular dystrophy, cardiovascular disease and cancer
title_full Translational implications of targeting annexin A2: From membrane repair to muscular dystrophy, cardiovascular disease and cancer
title_fullStr Translational implications of targeting annexin A2: From membrane repair to muscular dystrophy, cardiovascular disease and cancer
title_full_unstemmed Translational implications of targeting annexin A2: From membrane repair to muscular dystrophy, cardiovascular disease and cancer
title_short Translational implications of targeting annexin A2: From membrane repair to muscular dystrophy, cardiovascular disease and cancer
title_sort translational implications of targeting annexin a2 from membrane repair to muscular dystrophy cardiovascular disease and cancer
topic annexin
cancer
cardiovascular disease
membrane repair
muscular dystrophy
url https://doi.org/10.1002/ctd2.240
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