Wang Jinchuan, Wang Baozhen, Yin Yichen, Tian Nan, Li Tao
School of Clinical Medicine, Ningxia Medical University, Ningxia, China; Department of Surgical Oncology II, The General Hospital of Ningxia Medical University, 804 Shengli Street, Yinchuan, Ningxia 750004, China.
School of Clinical Medicine, Ningxia Medical University, Ningxia, China.
Crit Rev Eukaryot Gene Expr. 2025;35(5):1-16. doi: 10.1615/CritRevEukaryotGeneExpr.2025058112.
The HECT, C2, and WW domain-containing E3 ubiquitin protein ligase 1 (HECW1) gene is a member of the HECT family of E3 ubiquitin ligases. While HECW1 has been implicated in various cancers, its role in gastric cancer (GC) remains unclear.
Bioinformatics approaches were employed to investigate HECW1's role in GC. Functional assays, including the CCK-8, transwell migration, and wound healing assays, were performed to assess its impact on GC cell proliferation, invasion, and migration.
HECW1 expression was significantly upregulated in GC tissues compared to normal controls, correlating with specific clinical characteristics. Cox regression analyses identified HECW1 as an independent prognostic factor for GC. Prognostic nomograms accurately predicted 1-, 3-, and 5-year survival rates, with calibration curves closely aligned with the ideal diagonal line. Elevated HECW1 expression was associated with poorer overall survival and disease progression outcomes. ROC analyses demonstrated that HECW1 had strong predictive power for outcomes (AUC = 0.746, CI = 0.683-0.808) and five-year survival rates (AUC = 0.734, CI = 0.600-0.869). Enrichment analysis suggested HECW1's involvement in protein processing and interactions with substrates such as SMAD4, TTF1, DVL1, and NEDD4. Functional assays showed that HECW1 knockdown significantly reduced GC cell proliferation, invasion, and migration.
HECW1 acts as an oncogene in GC and represents a potential prognostic indicator. Targeting HECW1 may inhibit GC progression, providing a promising therapeutic strategy.
含HECT、C2和WW结构域的E3泛素蛋白连接酶1(HECW1)基因是E3泛素连接酶HECT家族的成员。虽然HECW1与多种癌症有关,但其在胃癌(GC)中的作用仍不清楚。
采用生物信息学方法研究HECW1在GC中的作用。进行了包括CCK-8、Transwell迁移和伤口愈合试验在内的功能试验,以评估其对GC细胞增殖、侵袭和迁移的影响。
与正常对照相比,GC组织中HECW1表达显著上调,与特定临床特征相关。Cox回归分析确定HECW1为GC的独立预后因素。预后列线图准确预测了1年、3年和5年生存率,校准曲线与理想对角线紧密对齐。HECW1表达升高与较差的总生存和疾病进展结果相关。ROC分析表明,HECW1对预后(AUC = 0.746,CI = 0.683-0.808)和五年生存率(AUC = 0.734,CI = 0.600-0.869)具有较强的预测能力。富集分析表明HECW1参与蛋白质加工以及与SMAD4、TTF1、DVL1和NEDD4等底物的相互作用。功能试验表明,敲低HECW1可显著降低GC细胞的增殖、侵袭和迁移。
HECW1在GC中起癌基因作用,是一种潜在的预后指标。靶向HECW1可能抑制GC进展,提供一种有前景的治疗策略。