AICAR and compound C negatively modulate HCC-induced primary human hepatic stellate cell activation in vitro.


Journal

American journal of physiology. Gastrointestinal and liver physiology
ISSN: 1522-1547
Titre abrégé: Am J Physiol Gastrointest Liver Physiol
Pays: United States
ID NLM: 100901227

Informations de publication

Date de publication:
01 04 2021
Historique:
pubmed: 7 1 2021
medline: 11 5 2021
entrez: 6 1 2021
Statut: ppublish

Résumé

Tumor stroma and microenvironment have been shown to affect hepatocellular carcinoma (HCC) growth, with activated hepatic stellate cells (HSC) as a major contributor in this process. Recent evidence suggests that the energy sensor adenosine monophosphate-activated kinase (AMPK) may mediate a series of essential processes during carcinogenesis and HCC progression. Here, we investigated the effect of different HCC cell lines with known

Identifiants

pubmed: 33406006
doi: 10.1152/ajpgi.00262.2020
doi:

Substances chimiques

CTNNB1 protein, human 0
Culture Media, Conditioned 0
Enzyme Activators 0
Protein Kinase Inhibitors 0
Pyrazoles 0
Pyrimidines 0
Ribonucleotides 0
TP53 protein, human 0
Tumor Suppressor Protein p53 0
beta Catenin 0
dorsomorphin 10K52CIC1Z
Aminoimidazole Carboxamide 360-97-4
AMPK alpha1 subunit, mouse EC 2.7.11.1
AMPK alpha2 subunit, mouse EC 2.7.11.1
PRKAA2 protein, human EC 2.7.11.1
AMP-Activated Protein Kinases EC 2.7.11.31
PRKAA1 protein, human EC 2.7.11.31
AICA ribonucleotide F0X88YW0YK

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

G543-G556

Auteurs

Katrin Böttcher (K)

Regenerative Medicine and Fibrosis Group, Institute for Liver and Digestive Health, University College London, Royal Free Campus, London, United Kingdom.
Sheila Sherlock Liver Centre, Royal Free Hospital, London, United Kingdom.

Lisa Longato (L)

Regenerative Medicine and Fibrosis Group, Institute for Liver and Digestive Health, University College London, Royal Free Campus, London, United Kingdom.

Giusi Marrone (G)

Regenerative Medicine and Fibrosis Group, Institute for Liver and Digestive Health, University College London, Royal Free Campus, London, United Kingdom.

Giuseppe Mazza (G)

Regenerative Medicine and Fibrosis Group, Institute for Liver and Digestive Health, University College London, Royal Free Campus, London, United Kingdom.

Leo Ghemtio (L)

Drug Research Program, Division of Pharmaceutical Biosciences, Faculty of Pharmacy, University of Helsinki, Helsinki, Finland.

Andrew Hall (A)

Sheila Sherlock Liver Centre, Royal Free Hospital, London, United Kingdom.
Department of Cellular Pathology, Royal Free Hospital, London, United Kingdom.

Tu Vinh Luong (TV)

Department of Cellular Pathology, Royal Free Hospital, London, United Kingdom.

Stefano Caruso (S)

Centre de Recherche des Cordeliers, INSERM, Functional Genomics of Solid Tumors Laboratory, Sorbonne Université, Université de Paris, Paris, France.

Benoit Viollet (B)

Université de Paris, Institut Cochin, CNRS, INSERM, Paris, France.

Jessica Zucman-Rossi (J)

Centre de Recherche des Cordeliers, INSERM, Functional Genomics of Solid Tumors Laboratory, Sorbonne Université, Université de Paris, Paris, France.
Hôpital Européen Georges Pompidou, Assistance Publique-Hôpitaux de Paris, Paris, France.

Massimo Pinzani (M)

Regenerative Medicine and Fibrosis Group, Institute for Liver and Digestive Health, University College London, Royal Free Campus, London, United Kingdom.
Sheila Sherlock Liver Centre, Royal Free Hospital, London, United Kingdom.

Krista Rombouts (K)

Regenerative Medicine and Fibrosis Group, Institute for Liver and Digestive Health, University College London, Royal Free Campus, London, United Kingdom.

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Classifications MeSH