RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:AXL: shapers of tumor progression and immunosuppressive microenvironments.
AXL: shapers of tumor progression and immunosuppressive microenvironments.
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随着研究的进展,我们对肿瘤微环境(TME)的理解发生了深刻变化。TME随着癌症的发展阶段和治疗干预的实施而演变,从免疫促进型微环境转变为免疫抑制型微环境。因此,我们密切关注TME在肿瘤增殖、转移和耐药性发展中的重要作用。AXL与肿瘤进展高度相关;然而,以往对AXL的研究仅限于其对癌细胞生物学行为的影响。越来越多的研究表明,AXL可以影响免疫细胞的功能和分化,介导免疫抑制,从而促进肿瘤生长。通过全面分析来识别和克服免疫抑制微环境的成因,代表了一种攻克癌症的新方法。在这篇综述中,我们着重阐明AXL在免疫抑制微环境中的作用,讨论并分析AXL对肿瘤细胞、T细胞、巨噬细胞、自然杀伤(NK)细胞、成纤维细胞及其他免疫基质细胞的影响。我们旨在从AXL在免疫微环境中的功能作用出发,阐明其对癌症进展和耐药的贡献。
As research progresses, our understanding of the tumor microenvironment (TME) has undergone profound changes. The TME evolves with the developmental stages of cancer and the implementation of therapeutic interventions, transitioning from an immune-promoting to an immunosuppressive microenvironment. Consequently, we focus intently on the significant role of the TME in tumor proliferation, metastasis, and the development of drug resistance. AXL is highly associated with tumor progression; however, previous studies on AXL have been limited to its impact on the biological behavior of cancer cells.
An increasing body of research now demonstrates that AXL can influence the function and differentiation of immune cells, mediating immune suppression and thereby fostering tumor growth. A comprehensive analysis to identify and overcome the causes of immunosuppressive microenvironments represents a novel approach to conquering cancer.
In this review, we focus on elucidating the role of AXL within the immunosuppressive microenvironments, discussing and analyzing the effects of AXL on tumor cells, T cells, macrophages, natural killer (NK) cells, fibroblasts, and other immune-stromal cells.
We aim to clarify the contributions of AXL to the progression and drug resistance of cancer from its functional role in the immune microenvironment.
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