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Fibroblast activation protein (FAP) as a prognostic biomarker in multiple tumors and its therapeutic potential in head and neck squamous cell carcinoma

RUIFANG LI1, XINRONG NAN2,*, MING LI3,*, OMAR RAHHAL3
1 School of Stomatology, Shanxi Medical University, Taiyuan, 030001, China
2 Department of Stomatology, The First Hospital of Shanxi Medical University, Taiyuan, 030001, China
3 Department of Oral and Maxillofacial Surgery, Xiangya Stomatology Hospital, Central South University, Changsha, 410005, China
* Corresponding Author: XINRONG NAN. Email: email; MING LI. Email: email

Oncology Research https://doi.org/10.32604/or.2024.046965

Received 20 October 2023; Accepted 02 February 2024; Published online 27 March 2024

Abstract

Background: Fibroblast activation protein (FAP), a cell surface serine protease, plays roles in tumor invasion and immune regulation. However, there is currently no pan-cancer analysis of FAP. Objective: We aimed to assess the pan-cancer expression profile of FAP, its molecular function, and its potential role in head and neck squamous cell carcinoma (HNSC). Methods: We analyzed gene expression, survival status, immune infiltration, and molecular functional pathways of FAP in The Cancer Genome Atlas (TCGA) and Genotype Tissue Expression (GTEx) tumors. Furthermore, to elucidate the role of FAP in HNSC, we performed proliferation, migration, and invasion assays post-FAP overexpression or knock-down. Results: FAP expression was elevated in nine tumor types and was associated with poor survival in eight of them. In the context of immune infiltration, FAP expression negatively correlated with CD8+ T-cell infiltration in five tumor types and positively with regulatory T-cell infiltration in four tumor types. Our enrichment analysis highlighted FAP’s involvement in the PI3K-Akt signaling pathway. In HNSC cells, FAP overexpression activated the PI3K-Akt pathway, promoting tumor proliferation, migration, and invasion. Conversely, FAP knockdown showed inhibitory effects. Conclusion: Our study unveils the association of FAP with poor tumor prognosis across multiple cancers and highlights its potential as a therapeutic target in HNSC.

Keywords

FAP; Head and neck squamous cell carcinoma; Cancer; Prognosis; Tumor microenvironment; Molecular function
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