TP53 缺失通过上调 NF-κB-IFN-β-MHC-Ia 信号促进骨肉瘤对 NK 细胞的抵抗
TP53 Loss Elevates NF-κB-IFN-β-MHC-Ia Signaling to Promote NK Cell Resistance in Osteosarcoma.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:The Tumor Stroma of Squamous Cell Carcinoma: A Complex Environment That Fuels Cancer Progression.
The Tumor Stroma of Squamous Cell Carcinoma: A Complex Environment That Fuels Cancer Progression.
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肿瘤微环境(TME)是由细胞和细胞外基质(ECM)成分组成的复杂集合体,在驱动肿瘤进展、塑造治疗反应和影响转移方面发挥着关键作用。本叙述性综述聚焦于皮肤鳞状细胞癌(cSCC)的肿瘤间质,重点阐述其关键组成成分及其动态贡献。
我们探讨了cSCC ECM中的显著变化——具体而言,即纤连蛋白、透明质酸、层粘连蛋白、蛋白聚糖和胶原蛋白的改变——如何促进癌症进展、转移和耐药。本文还探讨了cSCC TME的细胞组成,详细描述了癌症相关成纤维细胞(CAFs)、间充质干细胞(MSCs)、内皮细胞、周细胞、脂肪细胞及多种免疫细胞群体之间复杂的相互作用。这些多样化的参与者调控着肿瘤发展、血管生成和免疫反应。
最后,我们强调TME作为治疗靶点的潜力。本综述中讨论的新兴策略包括利用免疫系统(过继性细胞转移、检查点阻断)、抑制肿瘤血管生成、破坏CAF活性以及调控ECM成分。这些方法凸显了破译TME相互作用在推进cSCC治疗中所发挥的重要作用。
进一步阐明这些复杂关系的研究将揭示开发更有效cSCC治疗的新途径。
The tumor microenvironment (TME), a complex assembly of cellular and extracellular matrix (ECM) components, plays a crucial role in driving tumor progression, shaping treatment responses, and influencing metastasis. This narrative review focuses on the cutaneous squamous cell carcinoma (cSCC) tumor stroma, highlighting its key constituents and their dynamic contributions.
We examine how significant changes within the cSCC ECM-specifically, alterations in fibronectin, hyaluronic acid, laminins, proteoglycans, and collagens-promote cancer progression, metastasis, and drug resistance. The cellular composition of the cSCC TME is also explored, detailing the intricate interplay of cancer-associated fibroblasts (CAFs), mesenchymal stem cells (MSCs), endothelial cells, pericytes, adipocytes, and various immune cell populations. These diverse players modulate tumor development, angiogenesis, and immune responses.
Finally, we emphasize the TME's potential as a therapeutic target. Emerging strategies discussed in this review include harnessing the immune system (adoptive cell transfer, checkpoint blockade), hindering tumor angiogenesis, disrupting CAF activity, and manipulating ECM components. These approaches underscore the vital role that deciphering TME interactions plays in advancing cSCC therapy.
Further research illuminating these complex relationships will uncover new avenues for developing more effective treatments for cSCC.
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