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<p>Oral squamous cell carcinoma (OSCC) is one of the most common malignant tumors of the head and neck and is characterized by high heterogeneity and high recurrence rates. In particular, the serious side effects of radiotherapy and chemotherapy are the main obstacles in OSCC treatment. It is worth noting that immune infiltration is associated with the occurrence of OSCC. However, the effective induction of a robust immune response remains challenging because of the limited responsiveness of most patients with oral cancer. Celastrol (CeT) has excellent therapeutic efficacy against cancers, but is poorly soluble in water. We used RADA16-I hydrogel loaded with CeT (RADA-CeT) to improve its solubility and stability. The results indicated that the complex formed by the interaction between RADA16-I and CeT exhibited better stability, smaller particle size, excellent dispersibility, and high elasticity. Particularly, RADA-CeT hydrogel was more effective in activating damage-associated molecular patterns, thereby evoking immunogenic cell death (ICD) in OSCC cells. In vivo experiments demonstrated that RADA-CeT hydrogel had a stronger promoting effect on the expressions of CD4, CD8, calreticulin (CRT), and high-mobility group box-1 (HMGB1). Thus, RADA-CeT exhibited excellent anti-tumor efficacy by amplifying ICD. In the present study, we developed a biocompatible drug delivery system for uncaging the power of CeT in OSCC immunotherapy.</p>

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Self-assembling RADA16-I peptide in situ hydrogel loaded with Celastrol boost immunogenic cell death in oral squamous cell carcinoma

  • 期刊论文

  • 发表日期：

    2025年8月18日

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  • Chanjuan Zhang,
  • Jiajun Wu,
  • Hongfang Li,
  • Yaning Shi,
  • Yantian Liang,
  • Jingxin Chen,
  • Li Qin

摘要

Oral squamous cell carcinoma (OSCC) is one of the most common malignant tumors of the head and neck and is characterized by high heterogeneity and high recurrence rates. In particular, the serious side effects of radiotherapy and chemotherapy are the main obstacles in OSCC treatment. It is worth noting that immune infiltration is associated with the occurrence of OSCC. However, the effective induction of a robust immune response remains challenging because of the limited responsiveness of most patients with oral cancer. Celastrol (CeT) has excellent therapeutic efficacy against cancers, but is poorly soluble in water. We used RADA16-I hydrogel loaded with CeT (RADA-CeT) to improve its solubility and stability. The results indicated that the complex formed by the interaction between RADA16-I and CeT exhibited better stability, smaller particle size, excellent dispersibility, and high elasticity. Particularly, RADA-CeT hydrogel was more effective in activating damage-associated molecular patterns, thereby evoking immunogenic cell death (ICD) in OSCC cells. In vivo experiments demonstrated that RADA-CeT hydrogel had a stronger promoting effect on the expressions of CD4, CD8, calreticulin (CRT), and high-mobility group box-1 (HMGB1). Thus, RADA-CeT exhibited excellent anti-tumor efficacy by amplifying ICD. In the present study, we developed a biocompatible drug delivery system for uncaging the power of CeT in OSCC immunotherapy.