Multicompartment Polyion Complex Micelles Based on Triblock Polypept(o)ides Mediate Efficient siRNA Delivery to Cancer-Associated Fibroblasts for Antistromal Therapy of Hepatocellular Carcinoma.

desloratadine endosomal escape hepatocellular carcinoma polyion complex micelles polypept(o)ides siRNA co‐delivery

Journal

Advanced materials (Deerfield Beach, Fla.)
ISSN: 1521-4095
Titre abrégé: Adv Mater
Pays: Germany
ID NLM: 9885358

Informations de publication

Date de publication:
21 Jun 2024
Historique:
revised: 27 05 2024
received: 02 04 2024
medline: 3 7 2024
pubmed: 3 7 2024
entrez: 3 7 2024
Statut: aheadofprint

Résumé

Hepatocellular carcinoma (HCC) is the most frequent type of primary liver cancer and the third leading cause for cancer-related death worldwide. The tumor is difficult-to-treat due to its inherent resistance to chemotherapy. Antistromal therapy is a novel therapeutic approach, targeting cancer-associated fibroblasts (CAF) in the tumor microenvironment. CAF-derived microfibrillar-associated protein 5 (MFAP-5) is identified as a novel target for antistromal therapy of HCC with high translational relevance. Biocompatible polypept(o)ide-based polyion complex micelles (PICMs) constructed with a triblock copolymer composed of a cationic poly(l-lysine) complexing anti-MFAP-5 siRNA (siMFAP-5) via electrostatic interaction, a poly(γ-benzyl-l-glutamate) block loading cationic amphiphilic drug desloratatine (DES) via π-π interaction as endosomal escape enhancer and polysarcosine poly(N-methylglycine) for introducing stealth properties, are generated for siRNA delivery. Intravenous injection of siMFAP-5/DES PICMs significantly reduces the hepatic tumor burden in a syngeneic implantation model of HCC, with a superior MFAP-5 knockdown effect over siMFAP-5 PICMs or lipid nanoparticles. Transcriptome and histological analysis reveal that MFAP-5 knockdown inhibited CAF-related tumor vascularization, suggesting the anti-angiogenic effect of RNA interference therapy. In conclusion, multicompartment PICMs combining siMFAP-5 and DES in a single polypept(o)ide micelle induce a specific knockdown of MFAP-5 and demonstrate a potent antitumor efficacy (80% reduced tumor burden vs untreated control) in a clinically relevant HCC model.

Identifiants

pubmed: 38958110
doi: 10.1002/adma.202404784
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2404784

Subventions

Organisme : German Research Foundation
ID : SFB1066-3

Informations de copyright

© 2024 The Author(s). Advanced Materials published by Wiley‐VCH GmbH.

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Auteurs

Paul Schneider (P)

Department of Dermatology, University Medical Center of the Johannes Gutenberg-University, 55128, Mainz, Germany.

Heyang Zhang (H)

Division of BioTherapeutics, Leiden Academic Centre for Drug Research (LACDR), Leiden University, Leiden, 2333CC, Netherlands.

Leon Simic (L)

Department of Dermatology, University Medical Center of the Johannes Gutenberg-University, 55128, Mainz, Germany.
Division of BioTherapeutics, Leiden Academic Centre for Drug Research (LACDR), Leiden University, Leiden, 2333CC, Netherlands.

Zhuqing Dai (Z)

Division of BioTherapeutics, Leiden Academic Centre for Drug Research (LACDR), Leiden University, Leiden, 2333CC, Netherlands.

Barbara Schrörs (B)

Biosampling Unit, TRON gGmbH - Translational Oncology at the University Medical Center of the Johannes Gutenberg University, Freiligrathstr. 12, 55131, Mainz, Germany.

Özlem Akilli-Öztürk (Ö)

Biosampling Unit, TRON gGmbH - Translational Oncology at the University Medical Center of the Johannes Gutenberg University, Freiligrathstr. 12, 55131, Mainz, Germany.

Jian Lin (J)

Max Planck Institute for Polymer Research, Physics at Interphases, Ackermannweg 10, 55128, Mainz, Germany.

Feyza Durak (F)

Biosampling Unit, TRON gGmbH - Translational Oncology at the University Medical Center of the Johannes Gutenberg University, Freiligrathstr. 12, 55131, Mainz, Germany.

Jenny Schunke (J)

Department of Dermatology, University Medical Center of the Johannes Gutenberg-University, 55128, Mainz, Germany.

Vanessa Bolduan (V)

Department of Dermatology, University Medical Center of the Johannes Gutenberg-University, 55128, Mainz, Germany.

Bram Bogaert (B)

Ghent Research Group on Nanomedicines, Laboratory of General Biochemistry and Physical Pharmacy, Faculty of Pharmaceutical Sciences, Ghent University, Ghent, 9000, Belgium.

David Schwiertz (D)

Department of Dermatology, University Medical Center of the Johannes Gutenberg-University, 55128, Mainz, Germany.
Division of BioTherapeutics, Leiden Academic Centre for Drug Research (LACDR), Leiden University, Leiden, 2333CC, Netherlands.

Gabriela Schäfer (G)

Department of Dermatology, University Medical Center of the Johannes Gutenberg-University, 55128, Mainz, Germany.
Division of BioTherapeutics, Leiden Academic Centre for Drug Research (LACDR), Leiden University, Leiden, 2333CC, Netherlands.

Matthias Bros (M)

Department of Dermatology, University Medical Center of the Johannes Gutenberg-University, 55128, Mainz, Germany.

Stephan Grabbe (S)

Department of Dermatology, University Medical Center of the Johannes Gutenberg-University, 55128, Mainz, Germany.

Jörn Markus Schattenberg (JM)

Department of Medicine II, Saarland University Medical Center, Saarland University, 66421, Homburg, Germany.

Koen Raemdonck (K)

Ghent Research Group on Nanomedicines, Laboratory of General Biochemistry and Physical Pharmacy, Faculty of Pharmaceutical Sciences, Ghent University, Ghent, 9000, Belgium.

Kaloian Koynov (K)

Max Planck Institute for Polymer Research, Physics at Interphases, Ackermannweg 10, 55128, Mainz, Germany.

Mustafa Diken (M)

Biosampling Unit, TRON gGmbH - Translational Oncology at the University Medical Center of the Johannes Gutenberg University, Freiligrathstr. 12, 55131, Mainz, Germany.

Leonard Kaps (L)

Department of Dermatology, University Medical Center of the Johannes Gutenberg-University, 55128, Mainz, Germany.
Department of Medicine II, Saarland University Medical Center, Saarland University, 66421, Homburg, Germany.

Matthias Barz (M)

Department of Dermatology, University Medical Center of the Johannes Gutenberg-University, 55128, Mainz, Germany.
Division of BioTherapeutics, Leiden Academic Centre for Drug Research (LACDR), Leiden University, Leiden, 2333CC, Netherlands.

Classifications MeSH