Combining single-cell spatial transcriptomics and molecular simulation to develop in vivo probes targeting the perineural invasion region of adenoid cystic carcinoma

• Published in: Heliyon Vol. 10; no. 15; p. e34628
• Main Authors: Yuan, Xiaotian, Dong, Zijian, Zhang, Benjian, Li, Qinxuan, Jiang, Weihong
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 15-08-2024; Elsevier
• Subjects: Antigen presentation; Epitope peptide probe; Perineural invasion; Schwann cells; Single cell RNA sequencing; Space transcriptome sequencing; Antigen presentation; Space transcriptome sequencing; Epitope peptide probe; Perineural invasion; Schwann cells; Single cell RNA sequencing
• ISSN: 2405-8440; 2405-8440
• DOI: 10.1016/j.heliyon.2024.e34628

Perineural invasion (PNI) refers to the invasion, encasement, or penetration of tumor cells around or through nerves. Various malignant tumors, including pancreatic cancer, head and neck tumors, and bile duct cancer, exhibit the characteristic of PNI. Particularly, in head and neck-skull base tumors such as adenoid cystic carcinoma (ACC), PNI is a significant factor leading to incomplete surgical resection and postoperative recurrence.
Spatial transcriptomic and single-cell transcriptomic sequencing were conducted on a case of ACC tissue with PNI to identify potential probes targeting PNI. The efficacy of the probes was validated through in vivo and in vitro experiments.
Spatial transcriptomic and single-cell RNA sequencing revealed phenotypic changes in Schwann cells within the PNI region of ACC. Peptide probes were designed based on the antigen-presenting characteristics of Schwann cells in the PNI region, which are dependent on Major Histocompatibility Complex II (MHC-II) molecules. Successful validation in vitro and in vivo experiments confirmed that these probes can label viable Schwann cells in the PNI region, serving as a tool for dynamic in vivo marking of tumor invasion into nerves.
Peptide probes targeting Schwann cells' MHC-II molecules have the potential to demonstrate the occurrence of PNI in patients with ACC