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Blocking YAP1–Liprin-β2 interaction impedes metastasis and promotes tumor suppression in head and neck squamous carcinomaopen access

Authors
Woo, Seon RangNoh, Joo KyungLee, Min KyeongKong, MoonkyooMin, SoonkiSung, Ji-YounNa, KiyongKang, SuyeonHur, Junho K.Ko, Seong-GyuEun, Young-Gyu
Issue Date
Jul-2025
Publisher
NATURE PORTFOLIO
Keywords
Adaptor Proteins, Signal Transducing; Phosphoproteins; Transcription Factors; Yap-signaling Proteins; Yap1 Protein, Human; Phosphoprotein; Signal Transducing Adaptor Protein; Transcription Factor; Yap Signaling Protein; Yap1 Protein, Human; Cell Motion; Epithelial Mesenchymal Transition; Female; Gene Expression Regulation; Genetics; Head And Neck Squamous Cell Carcinoma; Head And Neck Tumor; Human; Metabolism; Metastasis; Pathology; Squamous Cell Carcinoma; Tumor Cell Line; Tumor Invasion; Adaptor Proteins, Signal Transducing; Carcinoma, Squamous Cell; Cell Line, Tumor; Cell Movement; Epithelial-mesenchymal Transition; Female; Gene Expression Regulation, Neoplastic; Head And Neck Neoplasms; Humans; Neoplasm Invasiveness; Neoplasm Metastasis; Phosphoproteins; Squamous Cell Carcinoma Of Head And Neck; Transcription Factors; Yap-signaling Proteins
Citation
SCIENTIFIC REPORTS, v.15, no.1, pp 1 - 13
Pages
13
Indexed
SCIE
SCOPUS
Journal Title
SCIENTIFIC REPORTS
Volume
15
Number
1
Start Page
1
End Page
13
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/212425
DOI
10.1038/s41598-025-11652-0
ISSN
2045-2322
Abstract
Our research investigates the role of the YAP1–PPFIBP2 axis in the epithelial–mesenchymal transition (EMT) and its subsequent impact on invasion and migration in head and neck squamous cell carcinoma (HNSCC). Utilizing both in vitro assays and genomic analyses, we demonstrate that YAP1 upregulates EMT by suppressing PPFIBP2/liprin-β2 expression. This regulatory pathway contributes to enhanced invasiveness and correlates with poorer prognostic outcomes in HNSCC. We specifically knocked down YAP1 in SNU1041 and SCC9 cell lines using siRNA, resulting in reduced invasion and migration. These effects were reversed by subsequent administration of siPPFIBP2. In contrast, overexpression of YAP1 in SCC25 cells led to increased EMT marker activity and enhanced invasive behavior, supporting the functional role of this axis. Importantly, pharmacological inhibition of YAP1 using CA3 led to a notable decrease in EMT markers, invasion, and migration, suggesting that blocking the YAP1–PPFIBP2 axis may serve as an effective therapeutic strategy in HNSCC. In conclusion, our study identifies the YAP1–PPFIBP2 interaction as a crucial mediator of tumor aggressiveness in HNSCC, offering new insight into metastatic progression and highlighting a promising target for therapeutic intervention.
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