Dual-stimuli responsive smart nanoprobe for precise diagnosis and synergistic multi-modalities therapy of superficial squamous cell carcinoma

• Published in: Journal of nanobiotechnology Vol. 21; no. 1; pp. 4 - 19
• Main Authors: Zhang, Peisen, Cui, Yingying, Wang, Jian, Cheng, Junwei, Zhu, Lichong, Liu, Chuang, Yue, Saisai, Pang, Runxin, Guan, Jiaoqiong, Xie, Bixia, Zhang, Ni, Qin, Meng, Jing, Lihong, Hou, Yi, Lan, Yue
• Format: Journal Article
• Language: English
• Published: London BioMed Central 03.01.2023; BioMed Central Ltd; BMC
• Subjects: Biotechnology; Carcinoma, Squamous Cell - diagnostic imaging; Carcinoma, Squamous Cell - drug therapy; Care and treatment; CD8-Positive T-Lymphocytes; Cell Line, Tumor; Chemistry; Chemistry and Materials Science; Design and construction; Diagnosis; Dual-stimuli responsive nanoprobe; Humans; Medical research; Medicine, Experimental; Methods; Molecular Medicine; Molecular probes; Molecular targeted therapy; Nanomedicine; Nanoparticles - chemistry; Nanoparticles - therapeutic use; Nanotechnology; Neoplasms - drug therapy; Phototherapy - methods; Precise diagnosis; Squamous cell carcinoma; Synergistic therapy; Tumor Microenvironment; Women in Nanobiotechnology; China; Precise diagnosis; Squamous cell carcinoma; Dual-stimuli responsive nanoprobe; Synergistic therapy
• ISSN: 1477-3155; 1477-3155
• DOI: 10.1186/s12951-022-01759-1

Background Although the promising advancements of current therapeutic approaches is available for the squamous cell carcinoma (SCC) patients, the clinical treatment of SCC still faces many difficulties. The surgical irreparable disfigurement and the postoperative wound infection largely hamper the recovery, and the chemo/radiotherapy leads to toxic side effects. Results Herein, a novel pH/Hyaluronidase (HAase) dual-stimuli triggered smart nanoprobe Fe III TA@HA has been designed through the biomineralization of Fe 3+ and polyphenol tannic acid (TA) under the control of hyaluronic acid (HA) matrix. With the HA residues on the outer surface, Fe III TA@HA nanoprobes can specifically target the SCC cells through the over-expressed CD44, and accumulate in the carcinoma region after intravenously administration. The abundant HAase in carcinoma microenvironment will trigger the degradation of HA molecules, thereby exposing the Fe III TA complex. After ingesting by tumor cells via CD44 mediated endocytosis, the acidic lysosomal condition will further trigger the protonation of TA molecules, finally leading to the Fe 3+ release of nanoprobe, and inducing a hybrid ferroptosis/apoptosis of tumor cells through peroxidase activity and glutathione depletion. In addition, Owing to the outstanding T 1 magnetic resonance imaging (MRI) performance and phototermal conversion efficiency of nanoprobes, the MRI-guided photothermal therapy (PTT) can be also combined to complement the Fe 3+ -induced cancer therapy. Meanwhile, it was also found that the nanoprobes can promote the recruitment of CD4 + and CD8 + T cells to inhibit the tumor growth through the cytokines secretion. In addition, the Fe III TA@HA nanoprobes can be eliminated from the body and no obvious adverse side effect can be found in histological analysis, which confirmed the biosafety of them. Conclusion The current Fe III TA@HA nanoprobe has huge potential in clinical translation in the field of precise diagnosis and intelligent synergistic therapy of superficial SCC. This strategy will promisingly avoid the surgical defects, and reduce the systemic side effect of traditional chemotherapy, paving a new way for the future SCC treatment. Graphical Abstract