family medicine forum 2008 toronto

family medicine forum 2008 toronto

Study sheds light on abnormal lipidome accumulation in hepatocellular carcinoma

A research group led by Prof. Piao Hailong from the Dalian Institute of Chemical Physics (DICP) of the Chinese Academy of Sciences (CAS) has identified the correlation between deubiquitinase ubiquitin-specific protease 22 (USP22) and abnormal lipidome accumulation in hepatocellular carcinoma (HCC).

They elucidated a USP22-regulated lipogenesis mechanism that involved the peroxisome proliferator-activated receptor gamma (PPARγ)—ATP citrate lyase (ACLY) / acetyl-CoA carboxylase (ACC) axis in HCC tumorigenesis, and provided a rationale for therapeutic targeting of lipogenesis via USP22 inhibition.

This study was published in Nature Communications on April 21. Prof. Xu Guowang from DICP and Prof. Tan Guang from the First Affiliated Hospital of Dalian Medical University were also involved in the study.

Metabolic reprogramming is one hallmark of cancer, among which the abnormally increased de novo lipogenesis (DNL) is one of the most common features.

Fatty acid synthesis occurs at a lower rate in nondividing cells, dosage ibuprofen 2 month old which mainly absorbs lipids from the extracellular circulation. In contrast, DNL, especially de novo fatty acid synthesis, is an important lipid source for cancer cells.

In this study, the researchers detected the expression of USP family members by immunoblotting in HCC tissues compared to paired normal adjacent tissues. They further screened different metabolites using liquid chromatography–mass spectrometry.

The results showed that USP22 was the most significantly highly-expressed USP member, and the high expression of USP22 was correlated with lipids and lipid-like metabolites upregulation.

Molecular and biochemical experiments confirmed USP22 regulated lipid metabolism through PPARγ, a ligand-activated transcription factor belonging to the nuclear hormone receptor family that promoted lipogenesis by upregulating lipid synthesis enzymes such as ACC, ACLY and fatty acid synthase (FASN).

PPARγ was the substrate of USP22 and USP22-mediated deubiquitination stabilized PPARγ and activated PPARγ target genes (i.e., ACC and ACLY), contributing to lipogenesis and HCC tumorigenesis.

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