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REVIEW article

Front. Immunol.

Sec. Cancer Immunity and Immunotherapy

Volume 16 - 2025 | doi: 10.3389/fimmu.2025.1626411

This article is part of the Research TopicCell Death: A New Frontier in Cancer ResearchView all 3 articles

A potential strategy to rebuild the tumor immune microenvironment : PANoptosis

Provisionally accepted
Siyu  WuSiyu WuBoyan  TianBoyan TianXueyang  PangXueyang PangBowen  SuiBowen Sui*
  • Heilongjiang University of Chinese Medicine, Harbin, China

The final, formatted version of the article will be published soon.

The convergence and interplay of pyroptosis, apoptosis, and necroptosis have led to the conceptualization of PANoptosis, an innovative paradigm of inflammatory programmed cell death. Characterized by the hierarchical assembly and activation of the PANoptosome, PANoptosis operates through tightly orchestrated signaling hubs and is intricately linked to organelle functionality. Accumulating evidence underscores its pivotal role in diverse oncogenic processes, positioning PANoptosis as a compelling frontier for antitumor therapeutic exploration. This review delineates the mechanistic underpinnings of PANoptosis, synthesizes its established contributions to tumor progression, and examines its dynamic crosstalk with the tumor immune microenvironment (TIME). Notably, we highlight recent breakthroughs in PANoptosis-driven immunotherapeutic strategies. We further propose that targeting PANoptosis to reprogram TIME represents a transformative approach in oncology, shifting the research paradigm from unimodal cell death regulation to multidimensional intervention. This perspective not only advances fundamental understanding but also holds significant promise for clinical translation, heralding a new era in cancer therapeutics.

Keywords: PANoptosis, Cell Death, Tumor immune microenvironment, Immunotherapy, Oncogenic process

Received: 10 May 2025; Accepted: 18 Jul 2025.

Copyright: © 2025 Wu, Tian, Pang and Sui. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Bowen Sui, Heilongjiang University of Chinese Medicine, Harbin, China

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