解读尤文氏肉瘤发病机制中的免疫景观:肿瘤浸润免疫细胞和免疫环境的作用

IF 3.4 2区 医学 Q2 Medicine
Rajiv Ranjan Kumar , Nikita Agarwal , Akshi Shree , Jaya Kanta Gorain , Ekta Rahul , Shuvadeep Ganguly , Sameer Bakhshi , Uttam Sharma
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引用次数: 0

摘要

尤文氏肉瘤(EwS)是第二常见的儿童骨恶性肿瘤,其特点是其侵袭性行为和不良预后。EwS的肿瘤微环境(TME)由免疫抑制成分形成,包括髓源性抑制细胞、肿瘤相关巨噬细胞和免疫检查点分子,如PD-1/PD-L1和HLA-G。这些因子通过调节肿瘤浸润性免疫细胞(如调节性T细胞(Tregs)、CD8+ T细胞和自然杀伤细胞)的功能,损害抗肿瘤免疫应答。趋化因子(包括CXCL9和CXCL12)和细胞因子(如转化生长因子- β和白细胞介素-10)进一步促进免疫抑制和转移传播。免疫治疗的最新进展强调了调节免疫细胞和信号通路以增强抗肿瘤免疫的治疗潜力。本文综述了EwS TME中复杂的免疫景观,重点介绍了关键免疫成分的机制作用及其作为治疗靶点的潜力。了解这些相互作用可以为创新治疗策略铺平道路,以改善EwS患者的临床结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Decoding the immune landscape in Ewing sarcoma pathogenesis: The role of tumor infiltrating immune cells and immune milieu
Ewing sarcoma (EwS) is the second most prevalent pediatric bone malignancy, characterized by its aggressive behavior and unfavorable prognosis. The tumor microenvironment (TME) of EwS is shaped by immunosuppressive components, including myeloid-derived suppressor cells, tumor-associated macrophages, and immune checkpoint molecules such as PD-1/PD-L1 and HLA-G. These elements impair anti-tumor immune responses by modulating the function of tumor-infiltrating immune cells, such as regulatory T cells (Tregs), CD8+ T cells, and natural killer cells. Chemokines, including CXCL9 and CXCL12, and cytokines, such as transforming growth factor-beta and interleukin-10, further contribute to immune suppression and promote metastatic dissemination. Recent advances in immunotherapy have highlighted the therapeutic potential of modulating immune cells and signaling pathways to enhance anti-tumor immunity. This review provides a comprehensive analysis of the complex immune landscape within the EwS TME, focusing on the mechanistic roles of key immune components and their potential as therapeutic targets. Understanding these interactions could pave the way for innovative treatment strategies to improve clinical outcomes in patients with EwS.
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来源期刊
CiteScore
7.20
自引率
2.90%
发文量
50
审稿时长
34 days
期刊介绍: The Journal of Bone Oncology is a peer-reviewed international journal aimed at presenting basic, translational and clinical high-quality research related to bone and cancer. As the first journal dedicated to cancer induced bone diseases, JBO welcomes original research articles, review articles, editorials and opinion pieces. Case reports will only be considered in exceptional circumstances and only when accompanied by a comprehensive review of the subject. The areas covered by the journal include: Bone metastases (pathophysiology, epidemiology, diagnostics, clinical features, prevention, treatment) Preclinical models of metastasis Bone microenvironment in cancer (stem cell, bone cell and cancer interactions) Bone targeted therapy (pharmacology, therapeutic targets, drug development, clinical trials, side-effects, outcome research, health economics) Cancer treatment induced bone loss (epidemiology, pathophysiology, prevention and management) Bone imaging (clinical and animal, skeletal interventional radiology) Bone biomarkers (clinical and translational applications) Radiotherapy and radio-isotopes Skeletal complications Bone pain (mechanisms and management) Orthopaedic cancer surgery Primary bone tumours Clinical guidelines Multidisciplinary care Keywords: bisphosphonate, bone, breast cancer, cancer, CTIBL, denosumab, metastasis, myeloma, osteoblast, osteoclast, osteooncology, osteo-oncology, prostate cancer, skeleton, tumour.
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