Iron Oxide Nanoparticles Functionalized with Fucoidan: a Potential Theranostic Nanotool for Hepatocellular Carcinoma.


Journal

Chembiochem : a European journal of chemical biology
ISSN: 1439-7633
Titre abrégé: Chembiochem
Pays: Germany
ID NLM: 100937360

Informations de publication

Date de publication:
17 08 2022
Historique:
revised: 24 06 2022
received: 06 05 2022
pubmed: 25 6 2022
medline: 20 8 2022
entrez: 24 6 2022
Statut: ppublish

Résumé

Fucoidan is a natural sulfated polysaccharide with a large range of biological activities including anticancer and anti-oxidation activities. Hepatocellular carcinoma is the fourth most common aggressive cancer type. The aim of this study was to investigate the bioactivity of free fucoidan versus its vectorization using nanoparticles (NPs) in human hepatoma cells, Huh-7. Iron oxide NPs were functionalized with fucoidan by a one-step surface complexation. NP cellular uptake was quantified by magnetic measurement at various extracellular iron concentrations. Cell invasion and migration were reduced with NPs while free fucoidan increases these events at low fucoidan concentration (≤0.5 μM). Concomitantly, a high decrease of reactive oxygen species production related with a decrease of the matrix metalloproteinase-9 activity and an increase of its expression was observed with NPs compared to free fucoidan. A proteomic analysis evidenced that some fucoidan regulated proteins appeared, which were related to protein synthesis, N-glycan processing, and cellular stress. To our knowledge, this is the first study which reveals such activity induced by fucoidan. These results pave the way for USPIO-fucoidan-NPs as potential theranostic nanotools for hepatocellular carcinoma treatment.

Identifiants

pubmed: 35748603
doi: 10.1002/cbic.202200265
doi:

Substances chimiques

Polysaccharides 0
fucoidan 9072-19-9

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e202200265

Informations de copyright

© 2022 Wiley-VCH GmbH.

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Auteurs

Frédéric Geinguenaud (F)

Université Sorbonne Paris Nord and Université Paris Cité, INSERM, LVTS, 75018, Paris, France.

Odile Sainte-Catherine (O)

Université Sorbonne Paris Nord and Université Paris Cité, INSERM, LVTS, 75018, Paris, France.

Florence Poirier (F)

Université Sorbonne Paris Nord, Plateforme PPUP13, 93000, Bobigny, France.

Valérie Besnard (V)

Université Sorbonne Paris Nord, H&P INSERM, UMR 1272, 93000, Bobigny, France.

Oualid Haddad (O)

Université Sorbonne Paris Nord and Université Paris Cité, INSERM, LVTS, 75018, Paris, France.

Frédéric Chaubet (F)

Université Sorbonne Paris Nord and Université Paris Cité, INSERM, LVTS, 75018, Paris, France.

Yoann Lalatonne (Y)

Université Sorbonne Paris Nord and Université Paris Cité, INSERM, LVTS, 75018, Paris, France.
Service de Biophysique et Médecine Nucléaire, AP-HP, Hôpital Avicenne, 9300, Bobigny, France.

Didier Lutomski (D)

Université Sorbonne Paris Nord, Plateforme PPUP13, 93000, Bobigny, France.

Angela Sutton (A)

Université Sorbonne Paris Nord and Université Paris Cité, INSERM, LVTS, 75018, Paris, France.
Service de Biochimie, AP-HP, Hôpital Jean Verdier, 93140, Bondy, France.

Laurence Motte (L)

Université Sorbonne Paris Nord and Université Paris Cité, INSERM, LVTS, 75018, Paris, France.

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