Parecoxib inhibits esophageal squamous cell carcinoma progression via the PDK1-AKT pathway

• Published in: Cellular & molecular biology letters 2022-03, Vol.27 (1), p.28-28
• Main Authors: Huang, Han-Ming, Huang, Xiao-Yu, Wu, Shao-Ping, Chen, Can-Keng, He, Xin-Hua, Zhang, Yong-Fa
• Format: Article
• Language: English
• Subjects: AKT protein; Analgesics; Cancer therapies; Cell culture; Cell cycle; Cell growth; Cell migration; Cell proliferation; Cholecystokinin; Cyclin B1; Cyclin-dependent kinase inhibitor p21; Enzymes; ESCC; Esophageal cancer; Experiments; Extracellular matrix; Flow cytometry; G2 phase; Gelatinase A; Matrix metalloproteinase; Medical prognosis; Metalloproteinase; Mutant p53; Nucleotide sequence; Parecoxib; PDK1–AKT; Phosphorylation; Research Letter; Sequence analysis; Signal transduction; Squamous cell carcinoma; Tumors; Western blotting; Wound healing
• ISSN: 1425-8153; 1689-1392
• DOI: 10.1186/s11658-022-00324-w

Parecoxib plays an important role in inhibition of human cancer. However, the effect of parecoxib on esophageal squamous cell carcinoma (ESCC) is still not well known. The purpose of this study was to investigate the effect of parecoxib on ESCC and its underlying mechanism. RNA-sequence analysis was performed to identify functional alterations and mechanisms. Cell cycle, proliferation, invasion, and migration were assessed using flow cytometry, CCK-8 assay, colony formation, transwell, and wound healing assays. Extracellular matrix (ECM) degradation was detected by substrate gel zymography and 3D cell culture assay. Western blotting was used to detect parecoxib-dependent mechanisms involving cell cycle, proliferation, invasion, and migration. Tumor formation in vivo was detected by mouse assay. Functional experiments indicated that parecoxib induced ESCC cell cycle arrest in G2 phase, and inhibited cell proliferation, invasion, and migration in vitro. Western blotting revealed that parecoxib downregulated the phosphorylation levels of AKT and PDK1, as well as the expression of the mutant p53, cyclin B1, and CDK1, while upregulating p21waf1. Parecoxib inhibited matrix metalloproteinase-2 (MMP2) secretion and invadopodia formation, which were related to ECM degradation. Furthermore, we found that parecoxib suppressed ESCC growth in heterotopic tumor models. Parecoxib inhibits ESCC progression, including cell cycle, proliferation, invasion, and migration, via the PDK1-AKT signaling pathway.