Chondroitin Sulfate‐Modified Hydroxyapatite for Caspase‐1 Activated Induced Pyroptosis through Ca Overload/ER Stress/STING/IRF3 Pathway in Colorectal Cancer

• Published in: Small (Weinheim an der Bergstrasse, Germany) Vol. 20; no. 43; pp. e2403201 - n/a
• Main Authors: Chen, Qing, Peng, Bin, Lin, Lifan, Chen, Jiawen, Jiang, Zhaojun, Luo, Yuanwei, Huang, Liyong, Li, Jin, Peng, Yuping, Wu, Jiaming, Li, Wei, Zhuang, Kangmin, Liang, Min
• Format: Journal Article
• Language: English
• Published: Germany Wiley Subscription Services, Inc 01.10.2024
• Subjects: Calcium; calcium overload; Cancer; Cell death; Cell membranes; Chondroitin sulfate; Colorectal cancer; Endoplasmic reticulum; Homeostasis; Hydroxyapatite; Interferon; Nanoparticles; Overloading; pyroptosis; Radiation therapy; Stimulators; STING; Surgical instruments; tumor immunotherapy; Tumors; pyroptosis; STING; colorectal cancer; calcium overload; tumor immunotherapy
• ISSN: 1613-6810; 1613-6829; 1613-6829
• DOI: 10.1002/smll.202403201

Immune checkpoint inhibitors, are the fourth most common therapeutic tool after surgery, chemotherapy, and radiotherapy for colorectal cancer (CRC). However, only a small proportion (≈5%) of CRC patients, those with “hot” (immuno‐activated) tumors, benefit from the therapy. Pyroptosis, an innovative form of programmed cell death, is a potentially effective means to mediate a “cold” to “hot” transformation of the tumor microenvironment (TME). Calcium‐releasing hydroxyapatite (HAP) nanoparticles (NPs) trigger calcium overload and pyroptosis in tumor cells. However, current limitations of these nanomedicines, such as poor tumor‐targeting capabilities and insufficient calcium (Ca) ion release, limit their application. In this study, chondroitin sulfate (CS) is used to target tumors via binding to CD44 receptors and kaempferol (KAE) is used as a Ca homeostasis disruptor to construct CS‐HAP@KAE NPs that function as pyroptosis inducers in CRC cells. CS‐HAP@KAE NPs bind to the tumor cell membrane, HAP released Ca in response to the acidic environment of the TME, and kaempferol (KAE) enhances the influx of extracellular Ca, resulting in intracellular Ca overload and pyroptosis. This is associated with excessive endoplasmic reticulum stress triggered activation of the stimulator of interferon genes/interferon regulatory factor 3 pathway, ultimately transforming the TME from “cold” to “hot”. CS‐HAP@KAE NPs selectively target CRC cells via CS‐CD44 interactions, triggering HAP‐mediated Ca release under TME stimuli. In addition, KAE perturbs Ca homeostasis, prompting extracellular Ca influx and intracellular Ca overload, which instigates ER stress and STING/IRF3 signaling. Consequently, NLRP3/caspase‐1/GSDMD axis activation elicits pyroptosis of tumor cells, secreting inflammatory mediators, converting the “cold” TME to “hot”, and potentiating CRC immunotherapy efficacy.