The altered lipidome of hepatocellular carcinoma. (November 2022)
- Record Type:
- Journal Article
- Title:
- The altered lipidome of hepatocellular carcinoma. (November 2022)
- Main Title:
- The altered lipidome of hepatocellular carcinoma
- Authors:
- Tan, Shawn Lu Wen
Israeli, Erez
Ericksen, Russell E.
Chow, Pierce K.H.
Han, Weiping - Abstract:
- Highlights: Lipidomics profiling and biochemical analyses of human HCCs reveal alterations in glycerophospholipid, sphingolipid, cholesterol and bile acid metabolism. Glycerophospholipid composition is commonly shifted towards increased MUFA-to-PUFA ratios in HCCs. Cholesterol esterification is augmented in HCCs. Loss of bile acid homeostasis occurs during hepatocarcinogenesis. Sphingolipid metabolism is often rewired to facilitate accumulation of sphingomyelins, sphingosine 1-phosphate and glycosphingolipids in HCCs. Abstract: Alterations in metabolic pathways are a hallmark of cancer. A deeper understanding of the contribution of different metabolites to carcinogenesis is thus vitally important to elucidate mechanisms of tumor initiation and progression to inform therapeutic strategies. Hepatocellular carcinoma (HCC) is a leading cause of cancer-related death worldwide and its altered metabolic landscape is beginning to unfold with the advancement of technologies. In particular, characterization of the lipidome of human HCCs has accelerated, and together with biochemical analyses, are revealing recurrent patterns of alterations in glycerophospholipid, sphingolipid, cholesterol and bile acid metabolism. These widespread alterations encompass a myriad of lipid species with numerous roles affecting multiple hallmarks of cancer, including aberrant growth signaling, metastasis, evasion of cell death and immunosuppression. In this review, we summarize the current trends andHighlights: Lipidomics profiling and biochemical analyses of human HCCs reveal alterations in glycerophospholipid, sphingolipid, cholesterol and bile acid metabolism. Glycerophospholipid composition is commonly shifted towards increased MUFA-to-PUFA ratios in HCCs. Cholesterol esterification is augmented in HCCs. Loss of bile acid homeostasis occurs during hepatocarcinogenesis. Sphingolipid metabolism is often rewired to facilitate accumulation of sphingomyelins, sphingosine 1-phosphate and glycosphingolipids in HCCs. Abstract: Alterations in metabolic pathways are a hallmark of cancer. A deeper understanding of the contribution of different metabolites to carcinogenesis is thus vitally important to elucidate mechanisms of tumor initiation and progression to inform therapeutic strategies. Hepatocellular carcinoma (HCC) is a leading cause of cancer-related death worldwide and its altered metabolic landscape is beginning to unfold with the advancement of technologies. In particular, characterization of the lipidome of human HCCs has accelerated, and together with biochemical analyses, are revealing recurrent patterns of alterations in glycerophospholipid, sphingolipid, cholesterol and bile acid metabolism. These widespread alterations encompass a myriad of lipid species with numerous roles affecting multiple hallmarks of cancer, including aberrant growth signaling, metastasis, evasion of cell death and immunosuppression. In this review, we summarize the current trends and findings of the altered lipidomic landscape of HCC and discuss their potential biological significance for hepatocarcinogenesis. … (more)
- Is Part Of:
- Seminars in cancer biology. Volume 86(2023)Part 3
- Journal:
- Seminars in cancer biology
- Issue:
- Volume 86(2023)Part 3
- Issue Display:
- Volume 86, Issue 3, Part 3 (2023)
- Year:
- 2023
- Volume:
- 86
- Issue:
- 3
- Part:
- 3
- Issue Sort Value:
- 2023-0086-0003-0003
- Page Start:
- 445
- Page End:
- 456
- Publication Date:
- 2022-11
- Subjects:
- BA bile acid -- BSH bile salt hydrolase -- cPLA2 cytosolic phospholipase A2 -- COX cyclooxygenase -- DEN diethylnitrosamine -- GlcCer glucosylceramide -- GPL glycerophospholipid -- HBV hepatitis B virus -- HCV hepatitis C virus -- HCC hepatocellular carcinoma -- iPLA2 calcium-independent phospholipase A2 -- LOX lipoxygenase -- LPA lysophosphatidic acid -- LPLD lysophospholipid -- MUFA monounsaturated fatty acid -- NAFLD non-alcoholic fatty liver disease -- NASH non-alcoholic steatohepatitis -- NKT natural killer T -- P450 cytochrome P450 -- PLA2 phospholipase A2 -- PDX patient-derived xenograft -- PUFA polyunsaturated fatty acid -- ROS reactive oxygen species -- SFA saturated fatty acid -- sPLA2 secretory phospholipase A2
Hepatocellular carcinoma -- Metabolism -- Cancer -- Lipidomics -- Lipid
Cancer -- Periodicals
Neoplasms -- Periodicals
Review Literature
Cancer -- Périodiques
Electronic journals
616.994 - Journal URLs:
- http://www.sciencedirect.com/science/journal/1044579X ↗
http://www.clinicalkey.com/dura/browse/journalIssue/1044579X ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/1044579X ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.semcancer.2022.02.004 ↗
- Languages:
- English
- ISSNs:
- 1044-579X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8239.448340
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 24508.xml