Nanoencapsulated senotherapeutic compounds targeting connexin-43 for enhanced wound healing

Oncological patients receiving radiotherapy or chemotherapy often experience impaired wound healing due to tissue damage and cellular senescence. Connexin43 (Cx43) is a key regulator in this process, promoting senescence and the SASP, which hinder regeneration. This study investigates targeting Cx43 in primary dermal fibroblasts from cancer patients using a new combination of nanoencapsulated drugs. We show that Cx43 overexpression correlates with reduced gap junction communication, increased senescence, and delayed healing. Treatment with oleuropein (OLP), a polyphenol with antioxidant and regenerative properties, restores fibroblast function, reduces senescence, and improves healing. We also examine the p38 MAPK inhibitor BIRB796, alone and with OLP, demonstrating its ability to suppress SASP and support tissue repair. After confirming the superior combined effect of OLP and BIRB796, we developed a co-encapsulated nanoformulation. This innovative approach may significantly enhance wound healing in oncological patients.

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Publication Details

Journal
iScience
Published
2025-12-26
DOI
https://doi.org/10.1016/j.isci.2025.114547
Primary Topic
Connexins and lens biology
Type
article
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article

Nanoencapsulated senotherapeutic compounds targeting connexin-43 for enhanced wound healing

Jenifer García-Fernández, Marina Rodríguez-Candela Mateos, Juan Pérez Cano, Sandra Alijas et al.
iScience
Connexins and lens biology
article

Nanoencapsulated senotherapeutic compounds targeting connexin-43 for enhanced wound healing

Jenifer García-Fernández, Marina Rodríguez-Candela Mateos, Juan Pérez Cano, Sandra Alijas, María de la Fuente, María Teresa Núñez Mayán, Maria Aurora Grimaudo, Sofia Saraiva, Luis Barrio, Varela-Eirín Marta, Benigno Acea Nebril, Adela Escudero
article en

Abstract

Oncological patients receiving radiotherapy or chemotherapy often experience impaired wound healing due to tissue damage and cellular senescence. Connexin43 (Cx43) is a key regulator in this process, promoting senescence and the SASP, which hinder regeneration. This study investigates targeting Cx43 in primary dermal fibroblasts from cancer patients using a new combination of nanoencapsulated drugs. We show that Cx43 overexpression correlates with reduced gap junction communication, increased senescence, and delayed healing. Treatment with oleuropein (OLP), a polyphenol with antioxidant and regenerative properties, restores fibroblast function, reduces senescence, and improves healing. We also examine the p38 MAPK inhibitor BIRB796, alone and with OLP, demonstrating its ability to suppress SASP and support tissue repair. After confirming the superior combined effect of OLP and BIRB796, we developed a co-encapsulated nanoformulation. This innovative approach may significantly enhance wound healing in oncological patients.

iScienceVol. 29(2)
Universidade da Coruña (ES), Universidade de Santiago de Compostela (ES), Instituto Cajal (ES), Complejo Hospitalario Universitario de Santiago (ES), Instituto Ramón y Cajal de Investigación Sanitaria (ES), Complexo Hospitalario Universitario A Coruña (ES), Instituto de Investigación Sanitaria de Santiago (ES), Centro de Investigación Biomédica en Red de Cáncer (ES), Instituto de Investigación Biomédica de A Coruña (ES), Acciona (Spain) (ES)
Openalex Percentile: Top 36%
Connexins and lens biology
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