NEDD4 is a biomarker of a poor prognosis that contributes to the progression and chemoresistance in small cell lung cancer.

IF 3.4 3区 生物学 Q3 CELL BIOLOGY
Cell Cycle Pub Date : 2025-05-01 Epub Date: 2025-08-06 DOI:10.1080/15384101.2025.2539657
Rong Gao, Yuting Bian, Yongguang Wang, Yani Zhang, Qizhi Zhu, Jinfu Nie, Zongtao Hu, Hongzhi Wang, Bo Hong
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引用次数: 0

Abstract

Small cell lung cancer (SCLC) accounts for approximately 15% of primary lung carcinomas and has the poorest outcome in all subtypes of lung cancer. The major hurdle for SCLC treatment failure is resistance to platinum-based chemotherapy. Therefore, an unmet need is to discover new targets that promote SCLC progression and chemoresistance. Based on the signature of ubiquitination-related genes (URGs), differentially expressed genes between cisplatin-resistant and cisplatin-sensitive SCLC cell lines were identified using the Genomics of Drug Sensitivity in Cancer (GDSC) database. The URGs associated with the prognosis were further screened by Cox and LASSO regression analyses, as well as a Kaplan-Meier survival analysis. The E3 ligase NEDD4 was identified to be associated with cisplatin resistance, poor prognosis and tumor metastasis in SCLC. The functional enrichment analysis indicated that the functions and pathways regulated by NEDD4 were enriched in cell proliferation, cell invasion, as well as ubiquitination and PI3K-AKT pathways in SCLC. The knockdown and overexpression of NEDD4 demonstrated that NEDD4 induced the phosphorylation of AKT in SCLC cells. Cell viability, wound healing and transwell invasion assays demonstrated that NEDD4 promoted the proliferation, chemoresistance and invasion of SCLC cells. These results suggest that NEDD4 is a biomarker of a poor prognosis for SCLC, and that it promotes AKT activation, SCLC progression and chemoresistance.

NEDD4是一个不良预后的生物标志物,有助于小细胞肺癌的进展和化疗耐药。
小细胞肺癌(SCLC)约占原发性肺癌的15%,在所有亚型肺癌中预后最差。SCLC治疗失败的主要障碍是对铂类化疗的耐药性。因此,尚未满足的需求是发现促进SCLC进展和化疗耐药的新靶点。基于泛素化相关基因(URGs)的特征,利用癌症药物敏感性基因组学(GDSC)数据库鉴定顺铂耐药和顺铂敏感SCLC细胞系之间的差异表达基因。通过Cox和LASSO回归分析以及Kaplan-Meier生存分析进一步筛选与预后相关的URGs。发现E3连接酶NEDD4与SCLC的顺铂耐药、预后不良和肿瘤转移有关。功能富集分析表明,NEDD4在SCLC细胞增殖、细胞侵袭、泛素化和PI3K-AKT通路中调控功能和通路富集。NEDD4的敲除和过表达表明,NEDD4诱导了SCLC细胞中AKT的磷酸化。细胞活力、伤口愈合和跨井侵袭实验表明,NEDD4促进了SCLC细胞的增殖、化疗耐药和侵袭。这些结果表明NEDD4是SCLC预后不良的生物标志物,它促进AKT激活、SCLC进展和化疗耐药。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cell Cycle
Cell Cycle 生物-细胞生物学
CiteScore
7.70
自引率
2.30%
发文量
281
审稿时长
1 months
期刊介绍: Cell Cycle is a bi-weekly peer-reviewed journal of high priority research from all areas of cell biology. Cell Cycle covers all topics from yeast to man, from DNA to function, from development to aging, from stem cells to cell senescence, from metabolism to cell death, from cancer to neurobiology, from molecular biology to therapeutics. Our goal is fast publication of outstanding research.
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