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CD36: The Bridge between Lipids and Tumors.

作者信息

Zhou Xuan, Su Manman, Lu Jungu, Li Deming, Niu Xinhui, Wang Yi

机构信息

Department of Regenerative Medicine, School of Pharmaceutical Sciences, Jilin University, Changchun 130012, China.

出版信息

Molecules. 2024 Jan 21;29(2):531. doi: 10.3390/molecules29020531.


DOI:10.3390/molecules29020531
PMID:38276607
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10819246/
Abstract

It has been found that the development of some cancers can be attributed to obesity, which is associated with the excessive intake of lipids. Cancer cells undergo metabolic reprogramming, shifting from utilizing glucose to fatty acids (FAs) for energy. CD36, a lipid transporter, is highly expressed in certain kinds of cancer cells. High expressions of CD36 in tumor cells triggers FA uptake and lipid accumulation, promoting rapid tumor growth and initiating metastasis. Meanwhile, immune cells in the tumor microenvironment overexpress CD36 and undergo metabolic reprogramming. CD36-mediated FA uptake leads to lipid accumulation and has immunosuppressive effects. This paper reviews the types of FAs associated with cancer, high expressions of CD36 that promote cancer development and progression, effects of CD36 on different immune cells in the tumor microenvironment, and the current status of CD36 as a therapeutic target for the treatment of tumors with high CD36 expression.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1736/10819246/8027bfaf398d/molecules-29-00531-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1736/10819246/cb44555e3952/molecules-29-00531-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1736/10819246/f6b97e23ec27/molecules-29-00531-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1736/10819246/17707661a6d7/molecules-29-00531-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1736/10819246/4d5892504ca8/molecules-29-00531-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1736/10819246/8027bfaf398d/molecules-29-00531-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1736/10819246/cb44555e3952/molecules-29-00531-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1736/10819246/f6b97e23ec27/molecules-29-00531-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1736/10819246/17707661a6d7/molecules-29-00531-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1736/10819246/4d5892504ca8/molecules-29-00531-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1736/10819246/8027bfaf398d/molecules-29-00531-g005.jpg

相似文献

[1]
CD36: The Bridge between Lipids and Tumors.

Molecules. 2024-1-21

[2]
Exogenous lipids promote the growth of breast cancer cells via CD36.

Oncol Rep. 2017-8-1

[3]
CD36: an emerging therapeutic target for cancer and its molecular mechanisms.

J Cancer Res Clin Oncol. 2022-7

[4]
CD36 and Its Role in Regulating the Tumor Microenvironment.

Curr Oncol. 2022-10-27

[5]
Lipid partitioning, incomplete fatty acid oxidation, and insulin signal transduction in primary human muscle cells: effects of severe obesity, fatty acid incubation, and fatty acid translocase/CD36 overexpression.

J Clin Endocrinol Metab. 2010-4-28

[6]
CD36-mediated metabolic crosstalk between tumor cells and macrophages affects liver metastasis.

Nat Commun. 2022-10-2

[7]
Endothelial cell CD36 optimizes tissue fatty acid uptake.

J Clin Invest. 2018-7-26

[8]
Fatty-acid receptor CD36 functions as a hydrogen sulfide-targeted receptor with its Cys333-Cys272 disulfide bond serving as a specific molecular switch to accelerate gastric cancer metastasis.

EBioMedicine. 2019-6-28

[9]
CD36 tango in cancer: signaling pathways and functions.

Theranostics. 2019-7-9

[10]
Inflammatory stress promotes the development of obesity-related chronic kidney disease via CD36 in mice.

J Lipid Res. 2017-7

引用本文的文献

[1]
Metabolic Adaptations in Cancer Progression: Optimization Strategies and Therapeutic Targets.

Cancers (Basel). 2025-7-15

[2]
PLIN2 promotes colorectal cancer progression through CD36-mediated epithelial-mesenchymal transition.

Cell Death Dis. 2025-7-10

[3]
Near-infrared fatty acid molecular probe for image-guided surgery of glioblastoma.

Npj Imaging. 2025-6-23

[4]
Human CD36: Gene Regulation, Protein Function, and Its Role in Atherosclerosis Pathogenesis.

Genes (Basel). 2025-6-13

[5]
Comparison Bioinformatic Analysis of Extracellular Vesicles-Related Genes and MicroRNAs in Breast Cancer.

Int J Mol Sci. 2025-6-19

[6]
Tumor Microenvironment, Inflammation, and Inflammatory Prognostic Indices in Diffuse Large B-Cell Lymphomas: A Narrative Review.

Int J Mol Sci. 2025-6-13

[7]
Targeting the tumour cell surface in advanced prostate cancer.

Nat Rev Urol. 2025-4-1

[8]
Aspirin impedes non-small cell lung cancer development via fine-tuning the CD36 localization regulated by GPIHBP1.

Transl Lung Cancer Res. 2025-2-28

[9]
Application of Carbon Nanomaterials to Enhancing Tumor Immunotherapy: Current Advances and Prospects.

Int J Nanomedicine. 2024

[10]
Histologic Characterization of Tumor-Adjacent Mammary Adipose Tissue in Normal-Weight and Overweight/Obese Patients with Triple-Negative Breast Cancer.

Cancers (Basel). 2024-10-17

本文引用的文献

[1]
Mediterranean diet and olive oil, microbiota, and obesity-related cancers. From mechanisms to prevention.

Semin Cancer Biol. 2023-10

[2]
Role of CD36 in cancer progression, stemness, and targeting.

Front Cell Dev Biol. 2022-12-8

[3]
CD36-mediated metabolic crosstalk between tumor cells and macrophages affects liver metastasis.

Nat Commun. 2022-10-2

[4]
CD36 accelerates the progression of hepatocellular carcinoma by promoting FAs absorption.

Med Oncol. 2022-9-29

[5]
Hypoxia-Induced CD36 Expression in Gastric Cancer Cells Promotes Peritoneal Metastasis via Fatty Acid Uptake.

Ann Surg Oncol. 2023-5

[6]
The complex role of tumor-infiltrating macrophages.

Nat Immunol. 2022-8

[7]
Association Between Dietary Fatty Acid Pattern and Risk of Oral Cancer.

Front Nutr. 2022-5-16

[8]
Targeting Gut Microbiota With Natural Polysaccharides: Effective Interventions Against High-Fat Diet-Induced Metabolic Diseases.

Front Microbiol. 2022-3-15

[9]
IL-6 promotes chemoresistance via upregulating CD36 mediated fatty acids uptake in acute myeloid leukemia.

Exp Cell Res. 2022-6-1

[10]
ω-3 and ω-6 Polyunsaturated Fatty Acids Regulate the Proliferation, Invasion and Angiogenesis of Gastric Cancer Through COX/PGE Signaling Pathway.

Front Oncol. 2022-2-17

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