A pyroptosis nanotuner for cancer therapy

Pyroptosis is a programmed cell death mechanism relevant in cancer therapy that can be triggered by endocytic organelle stress, but is challenging to induce in a controlled manner. In this paper the authors engineer a library of ultra-pH-sensitive nanophotosensitizers that can target specific endocytic organelles and elicit pyroptotic cancer cell death in a controlled fashion. Pyroptosis is a gasdermin-mediated programmed necrosis that occurs via membrane perforation and that can be exploited for biomedical applications in cancer therapy. However, inducing specific pyroptotic cancer cell death while sparing normal cells is challenging. Here, we report an acid-activatable nanophotosensitizer library that can be used to spatiotemporally target distinct stages of endosomal maturation, enabling tunable cellular pyroptosis. Specific activation of phospholipase C signalling transduction in early endosomes triggers gasdermin-E-mediated pyroptosis, which is dramatically reduced when acid-activatable nanophotosensitizers are transported into late endosomes/lysosomes. This nanotuner platform induces pyroptotic cell death with up to 40-fold tunability in various gasdermin-E-positive human cancers, resulting in enhanced anti-tumour efficacy and minimized systemic side effects. This study offers new insights into how to engineer nanomedicines with tunable pyroptosis activity through specific targeting of distinct endocytic signalling for biomedical applications.

Automated summary

The authors in this paper engineer a library of ultra-pH-sensitive nanophotosensitizers that can target specific endocytic organelles and induce pyroptotic cancer cell death in a controlled manner. By spatiotemporally targeting distinct stages of endosomal maturation, they achieve tunable cellular pyroptosis. The nanotuner platform demonstrates enhanced antitumor efficacy and minimized systemic side effects in various gasdermin-E-positive human cancers.