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癌症免疫治疗中靶向CD24

Targeting CD24 in Cancer Immunotherapy.

作者信息

Chen Wenwen, Hu Zhigang, Guo Zhigang

机构信息

Jiangsu Key Laboratory for Molecular and Medical Biotechnology, College of Life Sciences, Nanjing Normal University, 1 Wenyuan Road, Nanjing 210023, China.

出版信息

Biomedicines. 2023 Nov 27;11(12):3159. doi: 10.3390/biomedicines11123159.

DOI:10.3390/biomedicines11123159
PMID:38137380
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10740697/
Abstract

Immunotherapy is a hot area in cancer treatment, and one of the keys to this therapy is the identification of the right tumour-associated or tumour-specific antigen. Cluster of differentiation 24 (CD24) is an emerging tumour-associated antigen that is commonly and highly expressed in various tumours. In addition, CD24 is associated with several cancer-related signalling pathways and closely interacts with other molecules and immune cells to influence tumour progression. Monoclonal antibodies, antibody-drug conjugates (ADCs), chimeric antigen receptor (CAR) T-cell therapy, and CAR-NK cell therapy are currently available for the treatment of CD24. In this review, we summarise the existing therapeutic approaches and possible future directions targeting CD24.

摘要

免疫疗法是癌症治疗中的一个热门领域,而这种疗法的关键之一是识别合适的肿瘤相关或肿瘤特异性抗原。分化簇24(CD24)是一种新兴的肿瘤相关抗原,在各种肿瘤中普遍且高表达。此外,CD24与多种癌症相关信号通路有关,并与其他分子和免疫细胞密切相互作用以影响肿瘤进展。目前,单克隆抗体、抗体药物偶联物(ADC)、嵌合抗原受体(CAR)T细胞疗法和CAR-NK细胞疗法可用于治疗CD24。在本综述中,我们总结了针对CD24的现有治疗方法和可能的未来方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c6/10740697/dd615a60dbda/biomedicines-11-03159-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c6/10740697/8cc3150c5d8e/biomedicines-11-03159-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c6/10740697/c3abd40304d8/biomedicines-11-03159-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c6/10740697/4648c0f0bf7e/biomedicines-11-03159-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c6/10740697/dd615a60dbda/biomedicines-11-03159-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c6/10740697/8cc3150c5d8e/biomedicines-11-03159-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c6/10740697/c3abd40304d8/biomedicines-11-03159-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c6/10740697/4648c0f0bf7e/biomedicines-11-03159-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c6/10740697/dd615a60dbda/biomedicines-11-03159-g004.jpg

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本文引用的文献

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Mol Cell Biol. 2023;43(12):650-663. doi: 10.1080/10985549.2023.2285833. Epub 2023 Dec 20.
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Small-Molecule Fluorescent Ligands for the CXCR4 Chemokine Receptor.小分子荧光配体用于趋化因子受体 CXCR4。
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Emerging phagocytosis checkpoints in cancer immunotherapy.癌症免疫治疗中的新兴吞噬检查点。
巨噬细胞重编程癌症免疫疗法的临床现状。
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Coordinated activation of c-Src and FOXM1 drives tumor cell proliferation and breast cancer progression.c-Src 和 FOXM1 的协调激活驱动肿瘤细胞增殖和乳腺癌进展。
J Clin Invest. 2023 Apr 3;133(7):e162324. doi: 10.1172/JCI162324.
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PARP1 controls the transcription of CD24 by ADP-ribosylating the RNA helicase DDX5 in pancreatic cancer.在胰腺癌中,PARP1通过对RNA解旋酶DDX5进行ADP核糖基化来控制CD24的转录。
Int J Biochem Cell Biol. 2023 Feb;155:106358. doi: 10.1016/j.biocel.2022.106358. Epub 2022 Dec 28.
6
GATA3 Encapsulated by Tumor-Associated Macrophage-Derived Extracellular Vesicles Promotes Immune Escape and Chemotherapy Resistance of Ovarian Cancer Cells by Upregulating the CD24/Siglec-10 Axis.由肿瘤相关巨噬细胞衍生的细胞外囊泡包裹的GATA3通过上调CD24/Siglec-10轴促进卵巢癌细胞的免疫逃逸和化疗耐药性。
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