CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Unveiling the myxofibrosarcoma tumor microenvironment: implications for immunotherapy.
Unveiling the myxofibrosarcoma tumor microenvironment: implications for immunotherapy.
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黏液纤维肉瘤(MFS)是一种罕见且侵袭性强的软组织肉瘤,以高基因组不稳定性为特征,导致局部复发率高,晚期有效治疗选择有限。近年来癌症免疫学研究的进展推动了对包括MFS在内的肉瘤肿瘤微环境(TME)的探索,以寻找具有预后和治疗相关性的免疫相关生物标志物。尽管MFS中的数据仍然有限,现有证据提示其免疫景观具有异质性,包括:i)免疫检查点分子如程序性细胞死亡蛋白1(PD-1)和程序性死亡配体1(PD-L1)的表达差异,ii)TIL(肿瘤浸润淋巴细胞)的存在,iii)抗原呈递通路的改变,以及iv)显著的血管生成特征。这些发现强调了免疫生物标志物在患者临床分层中的潜在作用,以及由此开发新型免疫治疗策略的可能性。本综述将聚焦于免疫浸润、血管重塑和淋巴新生的细胞与分子架构,评估其作为潜在生物标志物的预后和预测价值。
最后,我们将介绍正在进行的旨在调控免疫-血管微环境的临床试验,为这一具有挑战性的肉瘤亚型提供创新治疗策略。
Myxofibrosarcoma (MFS) is a rare and aggressive soft tissue sarcoma characterized by high genomic instability, resulting in high local recurrence rates and limited effective therapeutic options in advanced stages. Recent progress in cancer immunology research has encouraged investigation into the Tumor Microenvironment (TME) of sarcomas, including MFS, to identify immune-related biomarkers of prognostic and therapeutic relevance.
Although data remain limited in MFS, existing evidence suggests a heterogeneous immune landscape, including: i) variable expression of immune checkpoint molecules such as Programmed Cell Death Protein 1 (PD-1) and Programmed Death-Ligand 1 (PD-L1), ii) presence of tumor-infiltrating lymphocytes, iii) alterations in antigen presentation pathways, and iv) a pronounced angiogenic signature.
These findings underscore the potential role of immune biomarkers for patients' clinical stratification and the consequent possibility of developing new immunotherapeutic strategies. This review will focus on the cellular and molecular architecture of immune infiltration, vascular remodeling, and lymphoid neogenesis, assessing their prognostic and predictive value as potential biomarkers.
Finally, we will present ongoing clinical trials aimed at modulating the immune-vascular niche to inform innovative therapeutic strategies for this challenging sarcoma subtype.
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