CD8+ T-cells |
|
Cholesterol content in tumor microenvironment increased expression of immune checkpoints leading to T-cell exhaustion. Cholesterol depletion restore the activity |
Ma et al., 2019 [87] |
Anticancer Tc9 cells (CD8+ T-cells) |
|
Cholesterol depletion increased antitumor activity |
Ma et al., 2018 [88] |
CD8+ T-cells |
|
Cholesterol in cancer cell’s plasma memrane decrease CD8+ cytotoxicity |
Lei et al., 2021 [89] |
CD8+ T-cells |
melanoma (in a mouse model) |
Inhibition of acetyl-CoA cholesterol acyltransferase increased proliferation of CD8+ T-cells |
Yang et al., 2016 [90] |
CD8+ T-cells |
Liver carcinoma cells |
Inhibition on cholesterol acyltransferase increased the amount of CD8+ T-cells and restorored CD8+ exhausted T-cell activity |
Schmidt et al., 2021 [91] |
T-cells |
breast cancer, colon cancer, and melanoma |
Inhibition of protein convertase subtilisin/kexin 9 decreased tumor growth and mortality in mice by reducing cholesterol metabolism and increasing T-cell infiltration in the tumors |
Liu et al., 2020 [92] |
Treg cells |
melanoma (in a mouse model) |
Lipid associated metabolic pathways by SREBP activity were enriched in tumors’ Treg cells. Inhibition of SREBP activity in Treg cells decreased tumor growth |
Lim et al., 2021 [83] |
T cells and tumor-associated macrophages |
|
Treg cells were able to activate tumor associated macrophages by modulating interferon γ secretion in CD8+ T-cells |
Liu et al., 2019 [84] |
CD4+ T-cells |
Prostate cancer |
Condition median from obesity-modified CD4+ T cells (decreased expression of IFNγ and IL-2 and increased expression of IL-6) increased the expression of epithelial-mesenchymal transition markers and showed a higher invasive and migratory capacity |
De Angulo et al., 2022 [94] |
Macrophages |
Prostate cancer |
Macrophages were associated with cholesterol transport and androgen synthesis in prostate cancer cells |
El-Kenawi et al., 2021 [95] |
Macrophages’ polarization |
|
In ABCG1 (transporter which efflux cholesterol from the cells) knockdown mouse strain, macrophage polarization switch from tumor-promoting M2 to anti-tumor-promoting M1 phenotype |
Sag et al., 2015 [96] |
Macrophages’ polarization |
|
Inhibition of ABCG1 in human macrophages switch polarization from tumor-promoting M2 to anti-tumor-promoting M1 phenotype. Stimulation with HDL also downregulated polarization to M1 phenotype |
Lee et al., 2016 [97] |
Macrophages |
Prostate cancer |
Cancer cell derived IL-1β enhanced expression of scavenger receptor, marco, on subset of macrophages. This was associated with prostate cancer progression and shorter disease-free survival. Marco was shown to regulate accumulation of lipids into the macrophages |
Masetti et al., 2022 [98] |
Myeloid-derived suppressor cells and macrophages |
Prostate cancer |
In mice fed with high-fat diet, number of myeloid-derived suppressor cells and ratio of M2/M1 macrophages were increased |
Hayashi et al., 2018 [99] |