» Articles » PMID: 37371076

The Role of CD36 in Cancer Progression and Its Value As a Therapeutic Target

Overview
Journal Cells
Publisher MDPI
Date 2023 Jun 28
PMID 37371076
Authors
Affiliations
Soon will be listed here.
Abstract

Cluster of differentiation 36 (CD36) is a cell surface scavenger receptor that plays critical roles in many different types of cancer, notably breast, brain, and ovarian cancers. While it is arguably most well-known for its fatty acid uptake functions, it is also involved in regulating cellular adhesion, immune response, and apoptosis depending on the cellular and environmental contexts. Here, we discuss the multifaceted role of CD36 in cancer biology, such as its role in mediating metastasis, drug resistance, and immune evasion to showcase its potential as a therapeutic target. We will also review existing approaches to targeting CD36 in pre-clinical studies, as well as discuss the only CD36-targeting drug to advance to late-stage clinical trials, VT1021. Given the roles of CD36 in the etiology of metabolic disorders, such as atherosclerosis, diabetes, and non-alcoholic fatty liver disease, the clinical implications of CD36-targeted therapy are wide-reaching, even beyond cancer.

Citing Articles

Prognostic significance and immune microenvironment infiltration patterns of hypoxia and endoplasmic reticulum stress-related genes in gastric cancer.

Li L, Liang Y, Xu W Front Oncol. 2025; 15:1542740.

PMID: 40061897 PMC: 11885130. DOI: 10.3389/fonc.2025.1542740.


Discovery and characterization of a human anti-CD36 scFv.

Mata-Cruz C, Guerrero-Rodriguez S, Gomez-Castellano K, Carballo-Uicab G, Almagro J, Perez-Tapia S Front Immunol. 2025; 16:1531171.

PMID: 39967671 PMC: 11832482. DOI: 10.3389/fimmu.2025.1531171.


CD36 inhibition enhances the anti-proliferative effects of PI3K inhibitors in PTEN-loss anti-HER2 resistant breast cancer cells.

Liu Y, Huang W, Wang S, Hsu H, Kao T, Chung W Cancer Metab. 2025; 13(1):6.

PMID: 39920872 PMC: 11806886. DOI: 10.1186/s40170-025-00375-5.


Dysregulation of genes involved in the long-chain fatty acid transport in pancreatic ductal adenocarcinoma.

Poenaru R, Milanesi E, Niculae A, Dobre A, Vladut C, Ciocirlan M World J Gastrointest Oncol. 2025; 17(1):98409.

PMID: 39817147 PMC: 11664611. DOI: 10.4251/wjgo.v17.i1.98409.


Monocyte-cancer cell fusion is mediated by phosphatidylserine-CD36 receptor interaction and induced by ionizing radiation.

Shabo I, Midtbo K, Branstrom R, Lindstrom A PLoS One. 2025; 20(1):e0311027.

PMID: 39752516 PMC: 11698428. DOI: 10.1371/journal.pone.0311027.


References
1.
Deng M, Cai X, Long L, Xie L, Ma H, Zhou Y . CD36 promotes the epithelial-mesenchymal transition and metastasis in cervical cancer by interacting with TGF-β. J Transl Med. 2019; 17(1):352. PMC: 6815430. DOI: 10.1186/s12967-019-2098-6. View

2.
Nath A, Chan C . Genetic alterations in fatty acid transport and metabolism genes are associated with metastatic progression and poor prognosis of human cancers. Sci Rep. 2016; 6:18669. PMC: 4698658. DOI: 10.1038/srep18669. View

3.
Yamashita S, Hirano K, Kuwasako T, Janabi M, Toyama Y, Ishigami M . Physiological and pathological roles of a multi-ligand receptor CD36 in atherogenesis; insights from CD36-deficient patients. Mol Cell Biochem. 2006; 299(1-2):19-22. DOI: 10.1007/s11010-005-9031-4. View

4.
Hrdinova T, Toman O, Dresler J, Klimentova J, Salovska B, Pajer P . Exosomes released by imatinib‑resistant K562 cells contain specific membrane markers, IFITM3, CD146 and CD36 and increase the survival of imatinib‑sensitive cells in the presence of imatinib. Int J Oncol. 2021; 58(2):238-250. DOI: 10.3892/ijo.2020.5163. View

5.
Yao C, Fowle-Grider R, Mahieu N, Liu G, Chen Y, Wang R . Exogenous Fatty Acids Are the Preferred Source of Membrane Lipids in Proliferating Fibroblasts. Cell Chem Biol. 2016; 23(4):483-93. PMC: 5510604. DOI: 10.1016/j.chembiol.2016.03.007. View