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:Lactate from the tumor microenvironment - A key obstacle in NK cell-based immunotherapies.
Lactate from the tumor microenvironment - A key obstacle in NK cell-based immunotherapies.
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关于乳酸新作用的最新发现改变了我们对这种糖酵解或发酵终产物的认识,它曾被认为只是一种废物。如今人们普遍认为,在葡萄糖受限的环境中,乳酸作为信号分子和癌细胞燃料来源发挥作用。此外,乳酸和乳酸脱氢酶是许多癌症预后不良的标志物,并调节免疫细胞的许多功能。肿瘤微环境(TME)中乳酸的存在导致树突状细胞免疫抑制表型的极化,并损害T细胞和NK细胞的细胞毒性能力,因此乳酸是免疫细胞效应功能和细胞免疫疗法疗效的主要障碍。新出现的证据表明,TME中的乳酸可能是一个新的治疗靶点,可增强细胞疗法的免疫治疗潜力。本综述描述了目前我们对乳酸在肿瘤生物学中作用的理解,包括其对癌症细胞免疫疗法的不利影响。我们还强调了在生产用于过继转移的细胞疗法时,必须考虑乳酸在TME中的作用,并描述了靶向调节TME中的乳酸如何可能增强免疫细胞功能并对细胞免疫疗法产生积极影响,重点关注NK细胞。
Recent findings about the new roles of lactate have changed our understanding of this end product of glycolysis or fermentation that was once considered only a waste product. It is now well accepted that lactate acts as a signaling molecule and fuel source for cancer cells in a glucose-restricted environment.
Moreover, lactate and lactate dehydrogenase are markers of poor prognosis of many cancers and regulate many functions of immune cells. The presence of lactate in the tumor microenvironment (TME) leads to polarization of the immunosuppressive phenotypes of dendritic cells and impairs the cytotoxic abilities of T cells and NK cells, and as such lactate is a major obstacle to immune-cell effector functions and the efficacy of cell-based immunotherapies.
Emerging evidence suggests that lactate in the TME might be a novel therapeutic target to enhance the immunotherapeutic potential of cell-based therapies. This review describes our current understanding of the role of lactate in tumor biology, including its detrimental effects on cell-based immunotherapy in cancer.
We also highlight how the role of lactate in the TME must be considered when producing cell therapies designed for adoptive transfer and describe how targeted modulation of lactate in the TME might boost immune-cell functions and positively impact cellular immunotherapy, with a focus on NK cell.
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