Cytokine & growth factor reviewsSep 19, 2025

Molecular Weaknesses in PANoptosis That Could Help Target Inflammatory Cell Death in Human Diseases

Alzheimers & Treatments Weekly Brief ↗PubMed ↗DOI ↗

Updated Jan 19, 2026

Abstract

PANoptosis is associated with a novel framework that integrates three types of inflammatory cell death through multiprotein complexes called PANoptosomes.

Emerging evidence indicates that pyroptosis, apoptosis, and necroptosis converge through shared sensors and signaling components.
Distinct innate immune sensors such as ZBP1, RIPK1, AIM2, and NLRP12 function as organizing hubs for the activation of PANoptosis.
The interplay between caspase-8, RIP kinases, and gasdermins suggests that PANoptosis operates as a flexible circuit for immune response and cell fate.
PANoptosis has protective roles in infections and tumor suppression but may also contribute to harmful effects in conditions like cytokine storms and neurodegeneration.
A comparative analysis across different organs and disease states highlights potential therapeutic targets in modulating PANoptotic pathways.

Simplified

PANoptosis represents a unified inflammatory cell death program that mechanistically integrates pyroptosis, apoptosis, and necroptosis through multiprotein complexes known as PANoptosomes. While prior models treated these death pathways as distinct, emerging evidence reveals their convergence through shared sensors, signaling adaptors, and executioners-allowing cells to bypass immune evasion strategies by pathogens or tumors. Despite its biological importance, a cohesive mechanistic framework for PANoptosis has remained elusive. In this review, we present a novel, sensor-specific dissection of PANoptosome architecture, detailing how distinct innate immune sensors-ZBP1, RIPK1, AIM2, and NLRP12 serve as organizing hubs for context-dependent activation of inflammatory cell death. We integrate this with a cross-pathway analysis of caspase-8, RIP kinases, and gasdermins, revealing PANoptosis as a highly adaptable logic circuit governing immune activation and cell fate. We further chart the dual roles of PANoptosis across disease contexts-highlighting its protective functions in infection and tumor suppression, as well as its detrimental consequences in cytokine storms, neurodegeneration, and multi-organ failure. By comparing sensor-driven outcomes across organs and disease states, we propose new therapeutic entry points for modulating PANoptotic signaling with precision. This review offers a mechanistically integrated and translationally focused roadmap to PANoptosis, establishing it as a master regulator of inflammatory cell death and a frontier for next-generation immune interventions.

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Competing interests

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

PubMed

Molecular Weaknesses in PANoptosis That Could Help Target Inflammatory Cell Death in Human Diseases

Abstract

Full Text

Funding

Competing interests

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