Carcinogenesis, Teratogenesis & Mutagenesis ›› 2025, Vol. 37 ›› Issue (2): 89-95,104.doi: 10.3969/j.issn.1004-616x.2025.02.001

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High expression of STMN3 and its oncogenic mechanism in esophageal squamous cell carcinoma

GUO Jing, XIE Guanchao, WANG Yinong, CAI Yan, ZHANG Yu, WANG Mingrong, HAO Jiajie   

  1. State Key Laboratory of Molecular Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China
  • Received:2025-01-05 Revised:2025-03-04 Online:2025-03-30 Published:2025-04-11

Abstract: OBJECTIVE:To investigate expression and mechanism of STMN3 in malignancy of esophageal squamous cell carcinoma (ESCC). METHODS:Expression of STMN3 in different tumors was analyzed in the TCGA database and its correlation with clinicopathological parameters was evaluated. CCLE database and Western blot were used to detect expression of STMN3 mRNA and protein levels in ESCC cell lines in vitro. Knockdown efficiency of STMN3 siRNA transfection in the cell lines was detected by RT-qPCR and Western blot,respectively. Effects of STMN3 on malignant phenotype of ESCC cells were detected by cell proliferation,colony formation,and cell apoptosis assays. The changes in the expression of proliferation-related proteins regulated by STMN3 were detected by Western blot. RESULTS:Compared with control group,STMN3 mRNA and protein were highly expressed in ESCC tissues and cell lines. STMN3 expression was associated with prognosis of patients,and those with high STMN3 expression had significantly worse prognosis (P<0.05). Knocking down STMN3 significantly inhibited the proliferation and colony formation of ESCC cells (P<0.01). In addition,the protein levels of EGFR and the phosphorylation levels of EGFR,S6,and SRC were significantly reduced. CONCLUSION:STMN3 was highly expressed in ESCC tissues,and STMN3 promoted the proliferation of ESCC cells by activating the EGFR-related signaling pathway.

Key words: STMN3, esophageal squamous cell carcinoma, cell proliferation, cell apoptosis, EGFR

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