CLSPN actives Wnt/β-catenin signaling to facilitate glycolysis and cell proliferation in oral squamous cell carcinoma

• Published in: Experimental cell research Vol. 435; no. 2; p. 113935
• Main Authors: Hou, Zeyu, Wu, Chenzhou, Tang, Jinru, Liu, Shaohua, Li, Longjiang
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 15.02.2024
• Subjects: Cell proliferation; CLSPN; Glycolysis; Oral squamous cell carcinoma; Wnt/β-catenin signaling pathway; Cell proliferation; Glycolysis; Oral squamous cell carcinoma; CLSPN; Wnt/β-catenin signaling pathway
• ISSN: 0014-4827; 1090-2422
• DOI: 10.1016/j.yexcr.2024.113935

Oral squamous cell carcinoma (OSCC) is a common malignancy with a poor prognosis. This study aimed to determine the influence and underlying mechanisms of CLSPN on OSCC. CLSPN expression was tested using quantitative real-time polymerase chain reaction, immunohistochemistry, and western blotting. Flow cytometry, cell counting kit, and colony formation assays were performed to determine OSCC cell apoptosis, viability, and proliferation, respectively. In OSCC cells, the extracellular acidification rate (ECAR), oxygen consumption rate (OCR), glucose uptake, and lactate production were determined using the corresponding kits. Changes in the protein levels of HK2, PKM2, LDHA, Wnt3a, and β-catenin were assessed using western blotting. CLSPN expression was increased in OSCC tissues. Overexpression of CLSPN in HSC-2 cells promoted cell proliferation, increased the levels of ECAR, glucose uptake, and lactate production, and increased the protein levels of HK2, PKM2, LDHA, Wnt3a, and β-catenin, but inhibited OCR levels and apoptosis. The knockdown of CLSPN in CAL27 cells resulted in the opposite results. Moreover, the effects of CLSPN overexpression on glycolysis and OSCC cell proliferation were reversed by Wnt3a knockdown. In vivo, knockdown of CLSPN restrained tumor growth, glycolysis, and the activation of Wnt/β-catenin signaling. CLSPN promoted glycolysis and OSCC cell proliferation, and reduced apoptosis, which was achieved by the activation of Wnt/β-catenin signaling pathway.