活力测定
波形蛋白
细胞迁移
化学
癌症研究
细胞生长
转染
上皮-间质转换
免疫印迹
下调和上调
细胞
庆大霉素保护试验
MTT法
分子生物学
生物
免疫学
基因
生物化学
免疫组织化学
作者
Hao Chen,Songtao Xue,Shuo‐Hui Cao,Jiarong Zhang,Yuanpu Wei,Chun Chen,Guobing Xu
标识
DOI:10.1096/fj.202500257r
摘要
ABSTRACT Esophageal squamous cell carcinoma (ESCC) is a highly invasive and metastatic malignancy. Circular RNAs (circRNAs), including hsa_circRNA_0101125, have been implicated in regulating cancer metastasis. But its potential roles in ESCC remain underexplored, particularly in relation to miR‐143‐3p. This study aimed to investigate the role of hsa_circRNA_0101125/miR‐143‐3p in the occurrence and development of ESCC. KYSE150 and ECA109 cells were used as in vitro models to evaluate the biological effects of hsa_circRNA_0101125. The interaction between ZNF148 and miR‐143‐3p was confirmed by dual‐luciferase assay. To assess the functional role of this pathway, cells were transfected with sh‐hsa_circRNA_0101125 vectors and/or miR‐143‐3p inhibitors, followed by assays for cell viability (CCK‐8), migration (wound healing assay), and invasion (Transwell assay). Transcriptions and expressions of hsa_circRNA_0101125, miR‐143‐3p, and ZNF148 were measured by RT‐qPCR and western blot. Results showed that hsa_circRNA_0101125 was localized in the cytoplasm and negatively regulated miR‐143‐3p, which targeted ZNF148. Inhibition of hsa_circRNA_0101125 significantly reduced cell viability, migration, and invasion, downregulated ZNF148 and Vimentin, and upregulated miR‐143‐3p and E‐cadherin expressions. In contrast, downregulating miR‐143‐3p abolished these effects. Therefore, hsa_circRNA_0101125 promotes the proliferation, migration, and invasion of ESCC cells by inhibiting the expression of miR‐143‐3p.
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