Polymeric nanoparticles for liver-targeted pituitary tumor-transforming gene 1 silencing in rats with chronic liver disease

Pituitary tumor transforming gene 1 (Pttg1) is upregulated in cirrhosis and hepatocarcinoma (HCC). We assessed the therapeutic effect of liver-targeted Pttg1 siRNA Retinol (Ret) pBAE nanoparticles (NPs) to treat these disturbances. Fibrosis was induced in Wistar rats by carbon tetrachloride inhalation and HCC by diethylnitrosamine injection. Ret pBAE NPs accumulated in hepatic tissue, close to zones positive for αSMA staining. Pttg1 interference increased mean arterial pressure, reduced portal hypertension and decreased collagen accumulation and inflammatory infiltrate in fibrotic rats. In HCC rats, Pttg1 silencing reduced liver to body weight ratio and hepatic proliferation and increased hepatic ATP production and serum glucose. This therapy effectively mitigated liver fibrosis and HCC progression in experimental models. The feasibility of this treatment was also demonstrated in human derived hepatic stellate cells and in ex vivo human cirrhotic livers underscoring the therapeutic potential of Pttg1 siRNA Ret pBAE NPs in addressing liver fibrosis and HCC.

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Publication Details

Journal
Nanomedicine Nanotechnology Biology and Medicine
Published
2025-09-25
DOI
https://doi.org/10.1016/j.nano.2025.102860
Citations
1
Primary Topic
Liver physiology and pathology
Type
article
Field-Weighted Citation Impact
1.32
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article

Polymeric nanoparticles for liver-targeted pituitary tumor-transforming gene 1 silencing in rats with chronic liver disease

Joana Faneca, Salvador Borrós, Wladimiro Jiménez, Gregori Casals et al.
1 citations
Nanomedicine Nanotechnology Biology and Medicine
Liver physiology and pathology
1.32
article

Polymeric nanoparticles for liver-targeted pituitary tumor-transforming gene 1 silencing in rats with chronic liver disease

Joana Faneca, Salvador Borrós, Wladimiro Jiménez, Gregori Casals, Judit García‐Villoria, Loreto Boix, Manuel Morales‐Ruiz, María Navalón-López, Meritxell Perramón, Guillermo Fernández‐Varo, Cristina Fornaguera, Yiliam Fundora, Manuel Macías-Herranz
article en
1 citations

Abstract

Pituitary tumor transforming gene 1 (Pttg1) is upregulated in cirrhosis and hepatocarcinoma (HCC). We assessed the therapeutic effect of liver-targeted Pttg1 siRNA Retinol (Ret) pBAE nanoparticles (NPs) to treat these disturbances. Fibrosis was induced in Wistar rats by carbon tetrachloride inhalation and HCC by diethylnitrosamine injection. Ret pBAE NPs accumulated in hepatic tissue, close to zones positive for αSMA staining. Pttg1 interference increased mean arterial pressure, reduced portal hypertension and decreased collagen accumulation and inflammatory infiltrate in fibrotic rats. In HCC rats, Pttg1 silencing reduced liver to body weight ratio and hepatic proliferation and increased hepatic ATP production and serum glucose. This therapy effectively mitigated liver fibrosis and HCC progression in experimental models. The feasibility of this treatment was also demonstrated in human derived hepatic stellate cells and in ex vivo human cirrhotic livers underscoring the therapeutic potential of Pttg1 siRNA Ret pBAE NPs in addressing liver fibrosis and HCC.

Nanomedicine Nanotechnology Biology and MedicineVol. 69
Hospital Clínic de Barcelona (ES), Institut Químic de Sarrià (ES), Fundació Clínic per a la Recerca Biomèdica (ES), Consorci Institut D'Investigacions Biomediques August Pi I Sunyer (ES), Universitat Ramon Llull (ES), Universitat de Barcelona (ES)
Openalex Percentile: Top 16%
Liver physiology and pathology
1.32
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