The high rates of aggressiveness, drug resistance and relapse of breast cancer (BC) are mainly attributed to the inability of conventional therapies to equally eradicate bulk differentiated cells and cancer stem cells (CSCs). To improve the effectiveness of BC treatments, we report the in-water synthesis of novel keratin-based nanoformulations, loaded with the CSC-specific drug salinomycin (SAL), the photosensitizer chlorin e6 (Ce6) and vitamin E acetate (SAL/Ce6@kVEs), which combine the capability of releasing SAL with the production of singlet oxygen upon light irradiation. In vitro experiments on BC cell lines and CSC-enriched mammospheres exposed to single or combined therapies showed that SAL/Ce6@kVEs determine synergistic cell killing, limit their self-renewal capacity and decrease the stemness potential by eradication of CSCs. In vivo experiments on zebrafish embryos confirmed the capacity of SAL nanoformulations to interfere with the Wnt/?-catenin signaling pathway, which is dysregulated in BC, thus identifying a target for further translation into pre-clinical models.

Keratin nanoparticles and photodynamic therapy enhance the anticancer stem cells activity of salinomycin

Guerrini Andrea
Co-primo
Conceptualization
;
Ferroni Claudia
Membro del Collaboration Group
;
Tedesco Daniele
Membro del Collaboration Group
;
Ballestri Marco
Membro del Collaboration Group
;
Varchi Greta
Penultimo
Conceptualization
;
2021

Abstract

The high rates of aggressiveness, drug resistance and relapse of breast cancer (BC) are mainly attributed to the inability of conventional therapies to equally eradicate bulk differentiated cells and cancer stem cells (CSCs). To improve the effectiveness of BC treatments, we report the in-water synthesis of novel keratin-based nanoformulations, loaded with the CSC-specific drug salinomycin (SAL), the photosensitizer chlorin e6 (Ce6) and vitamin E acetate (SAL/Ce6@kVEs), which combine the capability of releasing SAL with the production of singlet oxygen upon light irradiation. In vitro experiments on BC cell lines and CSC-enriched mammospheres exposed to single or combined therapies showed that SAL/Ce6@kVEs determine synergistic cell killing, limit their self-renewal capacity and decrease the stemness potential by eradication of CSCs. In vivo experiments on zebrafish embryos confirmed the capacity of SAL nanoformulations to interfere with the Wnt/?-catenin signaling pathway, which is dysregulated in BC, thus identifying a target for further translation into pre-clinical models.
2021
Istituto per la Sintesi Organica e la Fotoreattivita' - ISOF
Cancer stem cells
Chlorin e6
Keratin nanoparticle
Photodynamic therapy
Salinomycin
Zebrafish embryo
File in questo prodotto:
File Dimensione Formato  
prod_446599-doc_161059.pdf

solo utenti autorizzati

Descrizione: DOI: 10.1016/j.msec.2021.111899
Tipologia: Versione Editoriale (PDF)
Licenza: NON PUBBLICO - Accesso privato/ristretto
Dimensione 5.93 MB
Formato Adobe PDF
5.93 MB Adobe PDF   Visualizza/Apri   Richiedi una copia
prod_446599-doc_160637.pdf

Open Access dal 24/01/2022

Descrizione: Zenodo link: https://zenodo.org/records/8087237
Tipologia: Documento in Post-print
Licenza: Creative commons
Dimensione 1.41 MB
Formato Adobe PDF
1.41 MB Adobe PDF Visualizza/Apri
prod_446599-doc_160638.pdf

accesso aperto

Descrizione: Supplementary Material to DOI: 10.1016/j.msec.2021.111899
Tipologia: Altro materiale allegato
Licenza: Altro tipo di licenza
Dimensione 1.18 MB
Formato Adobe PDF
1.18 MB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/426217
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 9
  • ???jsp.display-item.citation.isi??? 8
social impact