Homeobox Protein BarH-like 1 Promotes Gastric Cancer Progression by Activating Coiled-Coil Domain-Containing Protein 178

被引:0
|
作者
Gu, Yue [1 ]
Chen, Gang [1 ]
Ning, Xinwei [1 ]
机构
[1] Harbin Med Univ, Affiliated Hosp 4, Dept Gen Surg, 37 Yiyuan St, Harbin 150001, Heilongjiang, Peoples R China
关键词
Gastric cancer; Macrophage; BARX1; CCDC178; ERK pathway; CARCINOMA; PROLIFERATION; METASTASIS;
D O I
10.1007/s10620-024-08312-0
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BackgroundCoiled-coil domain-containing protein 178 (CCDC178) has been revealed to exert metastasis-promoting properties in hepatocellular carcinoma, whereas its function in gastric cancer (GC) has not been fully understood.AimsWe evaluated its role in GC and the molecular mechanism.MethodsThe differentially expressed genes in datasets related to GC metastasis were intersected with survival-related genes in GC, followed by prognostic significance prediction. Loss- and gain-of-function assays were conducted to examine the involvement of CCDC178, Homeobox protein BarH-like 1 (BARX1), and the extracellular signal-regulated kinase (ERK) pathway in GC cell malignant phenotype and the polarization of tumor-associated macrophages (TAM). The corresponding functions were verified in the in vivo animal experiment.ResultsHigh CCDC178 expression predicted a poor prognosis for GC patients, and CCDC178 correlated significantly with macrophage infiltration in GC tissues. CCDC178 activated the ERK pathway in GC. Silencing of CCDC178 reduced the colony formation, migratory and invasive potential of GC cells, and the M2-like polarization of TAM, which was reversed by TBHQ (an ERK activator). BARX1 bound to the promoter region of CCDC178, thus inducing its transcriptional level. Silencing of BARX1 suppressed the M2-type polarization of TAM in vitro and in vivo, and CCDC178 mitigated the repressing role of BARX1 knockdown.ConclusionsBARX1 activates the transcription of CCDC178 to induce the ERK pathway, thereby supporting macrophage recruitment and M2-like polarization in GC.
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收藏
页码:1182 / 1199
页数:18
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