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从机制到治疗:CD24 在癌症中的作用。

From mechanism to therapy: the journey of CD24 in cancer.

机构信息

Department of Neurosurgery, The Affiliated Hospital of Qingdao University, Qingdao, China.

Department of Hand and Foot, The Affiliated Hospital of Qingdao University, Qingdao, China.

出版信息

Front Immunol. 2024 May 31;15:1401528. doi: 10.3389/fimmu.2024.1401528. eCollection 2024.


DOI:10.3389/fimmu.2024.1401528
PMID:38881902
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11176514/
Abstract

CD24 is a glycosylphosphatidylinositol-anchored protein that is expressed in a wide range of tissues and cell types. It is involved in a variety of physiological and pathological processes, including cell adhesion, migration, differentiation, and apoptosis. Additionally, CD24 has been studied extensively in the context of cancer, where it has been found to play a role in tumor growth, invasion, and metastasis. In recent years, there has been growing interest in CD24 as a potential therapeutic target for cancer treatment. This review summarizes the current knowledge of CD24, including its structure, function, and its role in cancer. Finally, we provide insights into potential clinical application of CD24 and discuss possible approaches for the development of targeted cancer therapies.

摘要

CD24 是一种糖基磷脂酰肌醇锚定蛋白,广泛表达于多种组织和细胞类型中。它参与多种生理和病理过程,包括细胞黏附、迁移、分化和凋亡。此外,CD24 在癌症中也得到了广泛研究,研究发现它在肿瘤生长、侵袭和转移中发挥作用。近年来,CD24 作为癌症治疗的潜在治疗靶点引起了越来越多的关注。本综述总结了 CD24 的现有知识,包括其结构、功能及其在癌症中的作用。最后,我们提供了对 CD24 潜在临床应用的见解,并讨论了开发针对癌症的靶向治疗方法的可能途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab44/11176514/f653782e648f/fimmu-15-1401528-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab44/11176514/a402b02e0b95/fimmu-15-1401528-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab44/11176514/8ed0742bacd7/fimmu-15-1401528-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab44/11176514/fc37d33d51b3/fimmu-15-1401528-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab44/11176514/254888143de8/fimmu-15-1401528-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab44/11176514/a084fc39d6e5/fimmu-15-1401528-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab44/11176514/f653782e648f/fimmu-15-1401528-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab44/11176514/a402b02e0b95/fimmu-15-1401528-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab44/11176514/8ed0742bacd7/fimmu-15-1401528-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab44/11176514/fc37d33d51b3/fimmu-15-1401528-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab44/11176514/254888143de8/fimmu-15-1401528-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab44/11176514/a084fc39d6e5/fimmu-15-1401528-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab44/11176514/f653782e648f/fimmu-15-1401528-g006.jpg

相似文献

[1]
From mechanism to therapy: the journey of CD24 in cancer.

Front Immunol. 2024

[2]
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[3]
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[4]
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[7]
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[8]
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[10]
CD24 interacts with and promotes the activity of c-src within lipid rafts in breast cancer cells, thereby increasing integrin-dependent adhesion.

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[2]
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Front Immunol. 2025-7-24

[3]
Dissecting the intratumoral microbiome landscape in lung cancer.

Front Immunol. 2025-7-24

[4]
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Front Immunol. 2025-4-17

[5]
SYL3C Aptamer-DNA Tetrahedra Conjugates Enable Near-Infrared Fluorescent Imaging of Colorectal Cancer.

Int J Nanomedicine. 2025-3-19

[6]
Impact of cannabinoids on cancer outcomes in patients receiving immune checkpoint inhibitor immunotherapy.

Front Immunol. 2025-3-5

[7]
Unraveling the triad of hypoxia, cancer cell stemness, and drug resistance.

J Hematol Oncol. 2025-3-18

[8]
The Immunoexpression and Prognostic Significance of Stem Cell Markers in Malignant Salivary Gland Tumors: A Systematic Review and Meta-Analysis.

Genes (Basel). 2024-12-29

本文引用的文献

[1]
IGSF8 is an innate immune checkpoint and cancer immunotherapy target.

Cell. 2024-5-23

[2]
Tumor Exosomal ENPP1 Hydrolyzes cGAMP to Inhibit cGAS-STING Signaling.

Adv Sci (Weinh). 2024-5

[3]
The Exonuclease TREX1 Constitutes an Innate Immune Checkpoint Limiting cGAS/STING-Mediated Antitumor Immunity.

Cancer Immunol Res. 2024-6-4

[4]
Checkpoint CD24 function on tumor and immunotherapy.

Front Immunol. 2024

[5]
IGSF8 is a potential target for the treatment of gliomas.

Asian J Surg. 2024-9

[6]
Intratumoral TREX1 Induction Promotes Immune Evasion by Limiting Type I IFN.

Cancer Immunol Res. 2024-6-4

[7]
Surprising magic of CD24 beyond cancer.

Front Immunol. 2024-1-19

[8]
Targeting CD24/Siglec-10 signal pathway for cancer immunotherapy: recent advances and future directions.

Cancer Immunol Immunother. 2024-1-27

[9]
Targeting the macrophage immunocheckpoint: a novel insight into solid tumor immunotherapy.

Cell Commun Signal. 2024-1-25

[10]
The Potential of Siglecs and Sialic Acids as Biomarkers and Therapeutic Targets in Tumor Immunotherapy.

Cancers (Basel). 2024-1-10

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