The influence of endothelial metabolic reprogramming on the tumor microenvironment

被引:2
|
作者
Kane, Kelby [1 ]
Edwards, Deanna [1 ,2 ,3 ]
Chen, Jin [1 ,2 ,3 ,4 ,5 ]
机构
[1] Vanderbilt Univ, Program Canc Biol, Nashville, TN 37235 USA
[2] Vanderbilt Univ, Med Ctr, Dept Med, Div Rheumatol, Nashville, TN 37235 USA
[3] Vanderbilt Univ, Med Ctr, Vanderbilt Ingram Canc Ctr, Nashville, TN 37235 USA
[4] Vanderbilt Univ, Dept Cell & Dev Biol, Nashville, TN 37235 USA
[5] Tennessee Valley Healthcare Syst, Dept Vet Affairs, Nashville, TN 37129 USA
关键词
GLYCOLYTIC ACTIVATOR PFKFB3; RENAL-CELL CARCINOMA; FATTY-ACID UPTAKE; VESSEL NORMALIZATION; VEGF-B; T-CELLS; GROWTH; CANCER; ANGIOGENESIS; MACROPHAGES;
D O I
10.1038/s41388-024-03228-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Endothelial cells (ECs) that line blood vessels act as gatekeepers and shape the metabolic environment of every organ system. In normal conditions, endothelial cells are relatively quiescent with organ-specific expression signatures and metabolic profiles. In cancer, ECs are metabolically reprogrammed to promote the formation of new blood vessels to fuel tumor growth and metastasis. In addition to EC's role on tumor cells, the tortuous tumor vasculature contributes to an immunosuppressive environment by limiting T lymphocyte infiltration and activity while also promoting the recruitment of other accessory pro-angiogenic immune cells. These elements aid in the metastatic spreading of cancer cells and contribute to therapeutic resistance. The concept of restoring a more stabilized vasculature in concert with cancer immunotherapy is emerging as a potential approach to overcoming barriers in cancer treatment. This review summarizes the metabolism of endothelial cells, their regulation of nutrient uptake and delivery, and their impact in shaping the tumor microenvironment and anti-tumor immunity. We highlight new therapeutic approaches that target the tumor vasculature and harness the immune response. Appreciating the integration of metabolic state and nutrient levels and the crosstalk among immune cells, tumor cells, and ECs in the TME may provide new avenues for therapeutic intervention.
引用
收藏
页码:51 / 63
页数:13
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