ANGPTL3, Apo CIII, Leptin and Triglycerides Are Elevated in Metastatic Prostate Cancer

BACKGROUND/OBJECTIVES: Prostate cancer (PCa) cells are known to heavily depend on lipids to support their growth. We hypothesized that hyperlipidemic factors, for which inhibitors are already available and used to treat cardiovascular disease, would be dysregulated in metastatic PCa (mPCa). The goal of this case-control study, including 35 men per group, was to compare the levels of PCSK9, ANGPTL3, Apo CIII, leptin, and the lipid profile in patients with mPCa versus localized Gleason 8/9 PCa (lPCa) and patients at risk of developing PCa (controls). METHODS: Protein levels were assessed using ELISAs, while lipids were measured using the Roche Cobas analytical platform. RESULTS: < 0.0001). Surprisingly, PCSK9 levels were negatively correlated with LDL in the entire cohort. CONCLUSIONS: In this cohort of men, whole-body lipid metabolic rewiring is a feature restricted to the metastatic phase of prostate cancer, suggesting it may play a significant role in the progression toward more aggressive cancer forms. Given the availability of drugs targeting ANGPTL3 and Apo CIII, the therapeutic potential of these drugs should be evaluated in metastatic PCa.

Authors

Institutions

Publication Details

Journal
Cancers
Published
2026-04-07
DOI
https://doi.org/10.3390/cancers18071176
Primary Topic
Lipid metabolism and disorders
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

ANGPTL3, Apo CIII, Leptin and Triglycerides Are Elevated in Metastatic Prostate Cancer

Frédéric Calon, Jonatan Blais, Vincent Fradet, Hélène Hovington et al.
Cancers
Lipid metabolism and disorders
article

ANGPTL3, Apo CIII, Leptin and Triglycerides Are Elevated in Metastatic Prostate Cancer

Frédéric Calon, Jonatan Blais, Vincent Fradet, Hélène Hovington, Alain Bergeron, Frédéric Pouliot, France‐Hélène Joncas, Emilie Wong Chong, Karine Robitaille, Nabil G. Seidah, Ann-Charlotte Bergeron, Gabriel Boulay, Chloé Castonguay, Marwan Khodr, Anne Gangloff
article en

Abstract

BACKGROUND/OBJECTIVES: Prostate cancer (PCa) cells are known to heavily depend on lipids to support their growth. We hypothesized that hyperlipidemic factors, for which inhibitors are already available and used to treat cardiovascular disease, would be dysregulated in metastatic PCa (mPCa). The goal of this case-control study, including 35 men per group, was to compare the levels of PCSK9, ANGPTL3, Apo CIII, leptin, and the lipid profile in patients with mPCa versus localized Gleason 8/9 PCa (lPCa) and patients at risk of developing PCa (controls). METHODS: Protein levels were assessed using ELISAs, while lipids were measured using the Roche Cobas analytical platform. RESULTS: < 0.0001). Surprisingly, PCSK9 levels were negatively correlated with LDL in the entire cohort. CONCLUSIONS: In this cohort of men, whole-body lipid metabolic rewiring is a feature restricted to the metastatic phase of prostate cancer, suggesting it may play a significant role in the progression toward more aggressive cancer forms. Given the availability of drugs targeting ANGPTL3 and Apo CIII, the therapeutic potential of these drugs should be evaluated in metastatic PCa.

CancersVol. 18(7)
Montreal Clinical Research Institute (CA), Université Laval (CA)
Fondation CHU de Québec, Canadian Institutes of Health Research, Natural Sciences and Engineering Research Council of Canada, Fonds de Recherche du Québec - Santé
Good health and well-being
Openalex Percentile: Top 29%
Lipid metabolism and disorders
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.