通过靶向肿瘤相关巨噬细胞的嵌合受体工程化溶瘤病毒重振内源性抗肿瘤免疫
Rejuvenating endogenous antitumor immunity via a chimeric receptor-engineered oncolytic virus targeting tumor-associated macrophages.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:miRNAs in Regulation of Tumor Microenvironment, Chemotherapy Resistance, Immunotherapy Modulation and miRNA Therapeutics in Cancer.
miRNAs in Regulation of Tumor Microenvironment, Chemotherapy Resistance, Immunotherapy Modulation and miRNA Therapeutics in Cancer.
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miRNA 是长度为 20-22 个核苷酸的非编码核糖核酸分子,对分子通路的调控至关重要。免疫逃逸和适宜肿瘤微环境的建立是支持肿瘤侵袭和转移的两个主要因素。致瘤性 miRNA 通过使重要的肿瘤敏感性调节细胞(如树突状细胞、M1 巨噬细胞和辅助性 T 细胞)对肿瘤脱敏,同时支持 Treg 细胞、促进自身耐受和慢性炎症的肿瘤相关 M2 巨噬细胞等免疫细胞的浸润和增殖,从而支持这两个标志性特征。miRNA 在增强癌症免疫治疗(如检查点阻断疗法、过继性 T 细胞疗法和溶瘤病毒疗法)的疗效方面具有重要作用。对 miRNA 作用的清晰理解可以帮助科学家制定更具针对性的治疗模式。miRNA 疗法已作为一类多样化的核酸类分子出现,能够抑制致癌 miRNA 并促进肿瘤抑制 miRNA 的表达。
miRNAs are 20-22 long nucleotide non-coding ribonucleic acid molecules critical to the modulation of molecular pathways. Immune evasion and the establishment of a suitable tumor microenvironment are two major contributors that support tumor invasion and metastasis. Tumorigenic miRNAs support these two hallmarks by desensitizing important tumor-sensitive regulatory cells such as dendritic cells, M1 macrophages, and T helper cells towards tumors while supporting infiltration and proliferation of immune cells like Treg cells, tumor-associated M2 macrophages that promote self-tolerance and chronic inflammation.
miRNAs have a significant role in enhancing the efficacies of immunotherapy treatments like checkpoint blockade therapy, adoptive T cell therapy, and oncolytic virotherapy in cancer. A clear understanding of the role of miRNA can help scientists to formulate better-targeted treatment modalities. miRNA therapeutics have emerged as diverse class of nucleic acid-based molecules that can suppress oncogenic miRNAs and promote the expression of tumor suppressor miRNAs.
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