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信号淋巴细胞激活分子家族受体:肿瘤进展的关键调节因子及癌症免疫治疗的新兴靶点

SLAMF receptors: key regulators of tumor progression and emerging targets for cancer immunotherapy.

作者信息

Li Jia, Fan Tao, Wang Di, Xiao Chu, Deng Ziqin, Cai Wenpeng, Ji Yu, Li Chunxiang, He Jie

机构信息

Department of Thoracic Surgery, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100021, China.

出版信息

Mol Cancer. 2025 May 17;24(1):145. doi: 10.1186/s12943-025-02308-8.


DOI:10.1186/s12943-025-02308-8
PMID:40382610
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12084948/
Abstract

The signaling lymphocytic activation molecule family (SLAMF) consists of nine distinct cell surface receptors predominantly expressed on immune cells, each characterized by unique structural features, expression patterns, downstream signaling pathways, and biological functions. These receptors play critical roles in modulating various immune cell activities within the tumor microenvironment, thereby shaping immune responses in cancer. Although accumulating evidence demonstrates their value as therapeutic targets for developing cancer immunotherapies, the full spectrum of SLAMF receptors in cancer remains incompletely understood. This review aims to provide a comprehensive overview of the molecular characteristics and immunomodulatory functions of each SLAMF receptor, underscoring their pivotal contributions to cancer progression. Furthermore, we also highlight their potential as promising targets for advancing cancer immunotherapeutic strategies. Finally, we discuss clinical trials evaluating the efficacy and safety of SLAMF receptor-based immunotherapies, emphasizing their translational relevance in the development of cancer treatments.

摘要

信号淋巴细胞激活分子家族(SLAMF)由九个不同的细胞表面受体组成,主要在免疫细胞上表达,每个受体都具有独特的结构特征、表达模式、下游信号通路和生物学功能。这些受体在调节肿瘤微环境中的各种免疫细胞活动中发挥关键作用,从而塑造癌症中的免疫反应。尽管越来越多的证据表明它们作为开发癌症免疫疗法的治疗靶点具有价值,但癌症中SLAMF受体的全貌仍未完全了解。本综述旨在全面概述每个SLAMF受体的分子特征和免疫调节功能,强调它们对癌症进展的关键贡献。此外,我们还强调了它们作为推进癌症免疫治疗策略的有前景靶点的潜力。最后,我们讨论评估基于SLAMF受体的免疫疗法疗效和安全性的临床试验,强调它们在癌症治疗开发中的转化相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a843/12084948/1ce60251f174/12943_2025_2308_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a843/12084948/ffe2965f3ae1/12943_2025_2308_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a843/12084948/b71f2868e12e/12943_2025_2308_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a843/12084948/2f8ac929d293/12943_2025_2308_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a843/12084948/21191b7c7822/12943_2025_2308_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a843/12084948/1ce60251f174/12943_2025_2308_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a843/12084948/ffe2965f3ae1/12943_2025_2308_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a843/12084948/b71f2868e12e/12943_2025_2308_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a843/12084948/2f8ac929d293/12943_2025_2308_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a843/12084948/21191b7c7822/12943_2025_2308_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a843/12084948/1ce60251f174/12943_2025_2308_Fig5_HTML.jpg

相似文献

[1]
SLAMF receptors: key regulators of tumor progression and emerging targets for cancer immunotherapy.

Mol Cancer. 2025-5-17

[2]
Signaling lymphocytic activation molecule family receptors as potential immune therapeutic targets in solid tumors.

Front Immunol. 2024

[3]
SLAM family-mediated crosstalk between tumor and immune cells in the tumor microenvironment: a promising biomarker and a potential therapeutic target for immune checkpoint therapies.

Clin Transl Oncol. 2025-3

[4]
A review: Mechanisms and molecular pathways of signaling lymphocytic activation molecule family 3 (SLAMF3) in immune modulation and therapeutic prospects.

Int Immunopharmacol. 2024-5-30

[5]
SLAMF receptors negatively regulate B cell receptor signaling in chronic lymphocytic leukemia via recruitment of prohibitin-2.

Leukemia. 2021-4

[6]
SLAMF8 can predict prognosis of pan-cancer and the immunotherapy response effectivity of gastric cancer.

Aging (Albany NY). 2024-5-22

[7]
The multifaceted role of CS1 (SLAMF7) in immunoregulation: Implications for cancer therapy and autoimmune disorders.

Exp Cell Res. 2025-4-1

[8]
Viral CD229 (Ly9) homologs as new manipulators of host immunity.

J Leukoc Biol. 2019-2-21

[9]
SLAM Family Receptors in B Cell Chronic Lymphoproliferative Disorders.

Int J Mol Sci. 2024-4-4

[10]
SLAMF receptors on normal and malignant B cells.

Clin Immunol. 2018-11-15

本文引用的文献

[1]
Signatures of H3K4me3 modification predict cancer immunotherapy response and identify a new immune checkpoint-SLAMF9.

Respir Res. 2025-1-15

[2]
Depletion of myeloid-derived suppressor cells sensitizes murine multiple myeloma to PD-1 checkpoint inhibitors.

J Immunother Cancer. 2025-1-4

[3]
CD84 as a therapeutic target for breaking immune tolerance in triple-negative breast cancer.

Cell Rep. 2024-11-26

[4]
CAR-T and CAR-NK as cellular cancer immunotherapy for solid tumors.

Cell Mol Immunol. 2024-10

[5]
CCL2 mediated IKZF1 expression promotes M2 polarization of glioma-associated macrophages through CD84-SHP2 pathway.

Oncogene. 2024-8

[6]
Preclinical activity of allogeneic SLAMF7-specific CAR T-cells (UCARTCS1) in multiple myeloma.

J Immunother Cancer. 2024-7-25

[7]
SLAMF8 can predict prognosis of pan-cancer and the immunotherapy response effectivity of gastric cancer.

Aging (Albany NY). 2024-5-22

[8]
A review: Mechanisms and molecular pathways of signaling lymphocytic activation molecule family 3 (SLAMF3) in immune modulation and therapeutic prospects.

Int Immunopharmacol. 2024-5-30

[9]
Phase 1 study combining elotuzumab with autologous stem cell transplant and lenalidomide for multiple myeloma.

J Immunother Cancer. 2024-4-12

[10]
SLAMF7 predicts prognosis and correlates with immune infiltration in serous ovarian carcinoma.

J Gynecol Oncol. 2024-11

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