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Targeting PKLR in liver diseases
KTH, Centres, Science for Life Laboratory, SciLifeLab. KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Protein Science, Systems Biology.ORCID iD: 0000-0002-9248-3294
KTH, Centres, Science for Life Laboratory, SciLifeLab. KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Protein Science, Systems Biology.ORCID iD: 0000-0001-8643-5846
KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Protein Science, Systems Biology. KTH, Centres, Science for Life Laboratory, SciLifeLab.ORCID iD: 0009-0002-0414-2471
Trustlife Labs, Drug Res & Dev Ctr, TR-34774 Istanbul, Turkiye.
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2025 (English)In: Trends in endocrinology and metabolism, ISSN 1043-2760, E-ISSN 1879-3061, Vol. 36, no 12, p. 1099-1110Article, review/survey (Refereed) Published
Abstract [en]

Pyruvate kinase is a key regulator in hepatic glucose metabolism, encoded by the gene pyruvate kinase liver/red blood cells (PKLR). Systems biology-based approaches, including metabolic and gene co-expression networks analyses, as well as genome-wide association studies (GWAS), have led to the identification of PKLR as a pivotal gene influencing liver metabolism in patients with metabolic dysfunction-associated steatotic liver disease (MASLD) and hepatocellular carcinoma (HCC). Here, we review the critical role of PKLR in MASLD and HCC progression and examine the effects of PKLR modulation both in vitro and in vivo. We also discuss the development of therapeutic strategies for patients with MASLD and HCC by modulating PKLR, highlighting its promising future in a broader range of liver diseases.

Place, publisher, year, edition, pages
Elsevier BV , 2025. Vol. 36, no 12, p. 1099-1110
National Category
Cell and Molecular Biology
Identifiers
URN: urn:nbn:se:kth:diva-376675DOI: 10.1016/j.tem.2025.03.009ISI: 001635591800001PubMedID: 40221236Scopus ID: 2-s2.0-105002666895OAI: oai:DiVA.org:kth-376675DiVA, id: diva2:2040932
Note

QC 20260223

Available from: 2026-02-23 Created: 2026-02-23 Last updated: 2026-02-23Bibliographically approved

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Yuan, MengShi, MengnanYang, HongZhang, ChengUhlén, MathiasAltay, ÖzlemMardinoglu, Adil

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Yuan, MengShi, MengnanYang, HongZhang, ChengUhlén, MathiasAltay, ÖzlemMardinoglu, Adil
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Trends in endocrinology and metabolism
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