4.7 Article

Non-apoptotic cell death induction via sapogenin based supramolecular particles

Journal

SCIENTIFIC REPORTS
Volume 12, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41598-022-17977-4

Keywords

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Funding

  1. Scientific and Technological Research Council of Turkey (TUBITAK) [118S709]
  2. Scientific Research Projects Coordination Unit of Izmir Institute of Technology (IZTECH BAP) [2017IYTE71]

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The discovery of novel chemotherapeutics that act through different mechanisms is crucial for addressing tumor heterogeneity and therapeutic resistance. This study further elucidates the unique cell death mechanism of AG-08 and its ability to form supramolecular particles. Through investigation of 18 analogs, the structural features required for the formation of particulate structures and stimulation of AG-08's unprecedented cell death mechanism were determined.
The discovery of novel chemotherapeutics that act through different mechanisms is critical for dealing with tumor heterogeneity and therapeutic resistance. We previously reported a saponin analog (AG-08) that induces non-canonical necrotic cell death and is auspicious for cancer therapy. Here, we describe that the key element in triggering this unique cell death mechanism of AG-08 is its ability to form supramolecular particles. These self-assembled particles are internalized via a different endocytosis pathway than those previously described. Microarray analysis suggested that AG-08 supramolecular structures affect several cell signaling pathways, including unfolded protein response, immune response, and oxidative stress. Finally, through investigation of its 18 analogs, we further determined the structural features required for the formation of particulate structures and the stimulation of the unprecedented cell death mechanism of AG-08. The unique results of AG-08 indicated that supramolecular assemblies of small molecules are promising for the field of anticancer drug development, although they have widely been accepted as nuisance in drug discovery studies.

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