# Lipoprotein Metabolism in Hematological Malignancies: A Role in Shaping the Tumor Cell Microenvironment?

**Authors:** Manal Sellam, Mélanie Lambert, Nadine Varin-Blank, Kevin Saitoski

PMC · DOI: 10.3390/metabo16020145 · 2026-02-20

## TL;DR

This paper reviews how lipoprotein metabolism influences the tumor microenvironment in blood cancers, potentially promoting tumor growth and immune suppression.

## Contribution

The paper provides a comprehensive review of lipoprotein metabolism's role in hematological malignancies and its impact on the tumor microenvironment.

## Key findings

- Lipoprotein metabolism contributes to an immune-suppressive tumor microenvironment in blood cancers.
- Abnormal lipoprotein levels are observed in leukemic patients, suggesting their importance for cancer cell survival.
- Cholesterol and fatty acids from lipoproteins support tumor progression by reprogramming metabolism.

## Abstract

The tumor microenvironment (TME) plays a key role in driving tumor progression, metastasis, and resistance to therapy. The TME is a highly variable ecosystem composed of both cancer and surrounding normal cells, immune survey cells and the extracellular matrix, also composed of signaling molecules that mediate interactions between them. Blood cancer cells pose a unique challenge because of their circulation and widespread distribution along with their capacity to invade various niches, interacting with a wide range of host cells such as fibroblasts, immune cells, endothelial cells, and adipocytes. Metabolism reprogramming in this tumor context, notably referring to elevated cholesterol and fatty acid metabolism, emerges as a crucial event in shaping an immune-suppressive microenvironment that promotes tumor progression. Cholesterol and fatty acids are supplied by both de novo biosynthesis and exogenous uptake from lipoproteins. Lipoproteins are pseudo-micellar structures, designed to transport essential water-insoluble metabolites, including triacylglycerols and cholesterol, in the plasma, lymph, and interstitial fluids. A number of studies have reported abnormal circulating lipoprotein levels in leukemic patients and have suggested that lipoproteins are key for cancer cells to thrive. However, the role of lipoprotein metabolism in cancer cells in the context of the TME is still incompletely discussed so far. The aim of this review is to consider the importance of lipoprotein metabolism in shaping the tumor microenvironment in the context of hematological malignancies.

## Linked entities

- **Diseases:** leukemia (MONDO:0004355)

## Full-text entities

- **Genes:** LDLR (low density lipoprotein receptor) [NCBI Gene 3949] {aka LDLCQ2}, LPL (lipoprotein lipase) [NCBI Gene 4023] {aka HDLCQ11, LIPD}, BCR (BCR activator of RhoGEF and GTPase) [NCBI Gene 613] {aka ALL, BCR1, CML, D22S11, D22S662, PHL}, IGHV3OR16-7 (immunoglobulin heavy variable 3/OR16-7 (pseudogene)) [NCBI Gene 28309] {aka IGHV3/OR16-7, IGHV3OR167}, SDC1 (syndecan 1) [NCBI Gene 6382] {aka CD138, SDC, SYND1, syndecan}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, VLDLR (very low density lipoprotein receptor) [NCBI Gene 7436] {aka CAMRQ1, CARMQ1, CHRMQ1, VLDL-R, VLDLRCH}, LIPC (lipase C, hepatic type) [NCBI Gene 3990] {aka HDLCQ12, HL, HTGL}, TLR7 (toll like receptor 7) [NCBI Gene 51284] {aka IMD74, SLEB17, TLR7-like}, APOB (apolipoprotein B) [NCBI Gene 338] {aka FCHL2, FLDB, LDLCQ4, apoB-100, apoB-48}, FASN (fatty acid synthase) [NCBI Gene 2194] {aka FAS, OA-519, SDR27X1}, APOA1 (apolipoprotein A1) [NCBI Gene 335] {aka AMYLD3, HPALP2, apo(a)}, SOAT1 (sterol O-acyltransferase 1) [NCBI Gene 6646] {aka ACACT, ACAT, ACAT-1, ACAT1, SOAT, STAT}, LPA (lipoprotein(a)) [NCBI Gene 4018] {aka AK38, APOA, LP}, CD40 (CD40 molecule) [NCBI Gene 958] {aka Bp50, CDW40, TNFRSF5, p50}, LIPG (lipase G, endothelial type) [NCBI Gene 9388] {aka EDL, EL, PRO719}, MPO (myeloperoxidase) [NCBI Gene 4353]
- **Diseases:** Burkitt's lymphoma (MESH:D002051), obesity (MESH:D009765), AML (MESH:D015470), metabolic disorders (MESH:D008659), Blood Cancer (MESH:D019337), lipoprotein abnormalities (MESH:C563618), Dyslipidemia (MESH:D050171), CLL (MESH:D015451), T-cell dysfunction (MESH:C536780), injury to (MESH:D014947), inflammatory (MESH:D007249), liver disease (MESH:D008107), CML (MESH:D015464), MM (MESH:D009101), diabetes (MESH:D003920), Cancer (MESH:D009369), aggressive (MESH:D010554), cholesterol (MESH:C535937), type 2 mellitus diabetes (MESH:D003924), lymphoma (MESH:D008223), lymphomatous (MESH:D013967), hypercholesterolemia (MESH:D006937), renal dysfunction (MESH:D007674), adiposity (MESH:D018205), lung, prostate and breast cancer (MESH:D001943), Richter transformed (MESH:C537025), DLBCL (MESH:D016403), Burkitt and Mantle cell lymphoma (MESH:D020522), Leukemias (MESH:D007938), atherosclerosis (MESH:D050197), metastasis (MESH:D009362), toxicity (MESH:D064420), familial hypercholesterolemia (MESH:D006938), cardiovascular disease (MESH:D002318), ALL (MESH:D054198), bone marrow adiposity (MESH:D001855)
- **Chemicals:** free fatty acids (MESH:D005230), bortezomib (MESH:D000069286), fludarabine (MESH:C024352), phospholipid (MESH:D010743), water (MESH:D014867), Cholesterol (MESH:D002784), mevalonate (MESH:D008798), TGs (MESH:D014280), Lipid (MESH:D008055), ixazomib (MESH:C548400), glutamine (MESH:D005973), glucose (MESH:D005947), orlistat (MESH:D000077403), 125I-LDL (-), palmitate (MESH:D010168), CEs (MESH:D002788), FA (MESH:D005227)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943734/full.md

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Source: https://tomesphere.com/paper/PMC12943734