Pyroptosis, a new bridge to tumor immunity.
Pyroptosis, a new bridge to tumor immunity.
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上睑下垂,通往肿瘤免疫的新桥梁。
DOI:
10.1111/cas.15059
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发表时间:
2021-10
期刊:
影响因子:
5.7
通讯作者:
Bai Y
中科院分区:
文献类型:
--
作者:
Li L;Jiang M;Qi L;Wu Y;Song D;Gan J;Li Y;Bai Y
Pyroptosis refers to the process of gasdermin (GSDM)‐mediated programmed cell death (PCD). Our understanding of pyroptosis has expanded beyond cells and is known to involve extracellular responses. Recently, there has been an increasing interest in pyroptosis due to its emerging role in activating the immune system. In the meantime, pyroptosis‐mediated therapies, which use the immune response to kill cancer cells, have also achieved notable success in a clinical setting. In this review, we discuss that the immune response induced by pyroptosis activation is a double‐edged sword that affects all stages of tumorigenesis. On the one hand, the activation of inflammasome‐mediated pyroptosis and the release of pyroptosis‐produced cytokines alter the immune microenvironment and promote the development of tumors by evading immune surveillance. On the other hand, pyroptosis‐produced cytokines can also collect immune cells and ignite the immune system to improve the efficiency of tumor immunotherapies. Pyroptosis is also related to some immune checkpoints, especially programmed death‐1 (PD‐1) or programmed death‐ ligand 1 (PD‐L1). In this review, we mainly focus on our current understanding of the interplay between the immune system and tumors that process through pyroptosis, and debate their use as potential therapeutic targets. The immune response induced by pyroptosis activation is a double‐edged sword that affects all stages of tumorigenesis. On the one hand, the activation of inflammasome‐mediated pyroptosis and the release of pyroptosis‐produced cytokines alter the immune microenvironment and promote the development of tumors by evading immune surveillance. On the other hand, pyroptosis‐produced cytokines can also collect immune cells and ignite the immune system to improve the efficiency of tumor immunotherapies.
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DOI:
10.1084/jem.20161707
发表时间:
2017-06-05
期刊:
The Journal of experimental medicine
影响因子:
--
作者:
Daley D;Mani VR;Mohan N;Akkad N;Pandian GSDB;Savadkar S;Lee KB;Torres-Hernandez A;Aykut B;Diskin B;Wang W;Farooq MS;Mahmud AI;Werba G;Morales EJ;Lall S;Wadowski BJ;Rubin AG;Berman ME;Narayanan R;Hundeyin M;Miller G
通讯作者:
Miller G
影响因子:
82.9
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通讯作者:
Krummel MF
DOI:
10.2119/molmed.2014.00232
发表时间:
2014-12-16
期刊:
Molecular medicine (Cambridge, Mass.)
影响因子:
--
作者:
Dinarello, Charles Anthony
通讯作者:
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影响因子:
3.8
作者:
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通讯作者:
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影响因子:
28.2
作者:
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通讯作者:
Aplin, Andrew E.