靶向PKLR治疗肝脏疾病

Meng Yuan, Mengnan Shi, Hong Yang, Sajda Ashraf, Shazia Iqbal, Hasan Turkez, Jan Boren, Cheng Zhang, Mathias Uhlén, Ozlem Altay, Adil Mardinoglu
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引用次数: 0

摘要

丙酮酸激酶是肝脏葡萄糖代谢的关键调节因子,由丙酮酸激酶肝/红细胞(PKLR)基因编码。基于系统生物学的方法,包括代谢和基因共表达网络分析,以及全基因组关联研究(GWAS),已经确定PKLR是影响代谢功能障碍相关脂肪变性肝病(MASLD)和肝细胞癌(HCC)患者肝脏代谢的关键基因。在这里,我们回顾了PKLR在MASLD和HCC进展中的关键作用,并检查了PKLR调节在体外和体内的作用。我们还讨论了通过调节plklr治疗MASLD和HCC患者的治疗策略的发展,强调了其在更广泛的肝脏疾病中的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeting PKLR in liver diseases
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.
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