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CD8 T细胞加剧癌症铁死亡的“火势”。

CD8 T cells PUF(A)ing the flames of cancer ferroptotic cell death.

作者信息

Friedmann Angeli José Pedro, Xavier da Silva Thamara Nishida, Schilling Bastian

机构信息

Rudolf-Virchow-Zentrum Center for Integrative and Translational Bioimaginng, University of Würzburg, Würzburg, Germany.

Rudolf-Virchow-Zentrum Center for Integrative and Translational Bioimaginng, University of Würzburg, Würzburg, Germany.

出版信息

Cancer Cell. 2022 Apr 11;40(4):346-348. doi: 10.1016/j.ccell.2022.03.003. Epub 2022 Mar 24.

DOI:10.1016/j.ccell.2022.03.003
PMID:35334204
Abstract

In this issue of Cancer Cell, Liao et al. demonstrate that CD8 T cell-secreted interferon-gamma (IFN-γ) rewires cancer cell lipid metabolism via the enzyme acyl-CoA synthetase long-chain family member 4 (ACSL4). ACSL4 activates polyunsaturated fatty acids and sensitizes cancer cells to ferroptosis in immunotherapy-relevant settings. These findings provide insights into how the metabolic and immune milieu could be used to promote ferroptosis.

摘要

在本期《癌细胞》杂志中,廖等人证明,CD8 T细胞分泌的γ干扰素(IFN-γ)通过酰基辅酶A合成酶长链家族成员4(ACSL4)改变癌细胞的脂质代谢。在免疫治疗相关环境中,ACSL4激活多不饱和脂肪酸并使癌细胞对铁死亡敏感。这些发现为如何利用代谢和免疫环境促进铁死亡提供了见解。

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CD8 T cells and fatty acids orchestrate tumor ferroptosis and immunity via ACSL4.CD8 T 细胞和脂肪酸通过 ACSL4 调控肿瘤铁死亡和免疫。
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