The Ubiquitin E3 Ligase FBXO33 Suppresses Stem Cell-Like Properties and Metastasis in Non-Small-Cell Lung Cancer by Promoting Ubiquitination and Degradation of Myc.

IF 3.3 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Frontiers in bioscience (Landmark edition) Pub Date : 2024-08-21 DOI:10.31083/j.fbl2908296
Qiong Wei, Zichun Liu, Jing Zhu, Wenyan Jiang, Haiqin Xie, Ganzhu Feng, Keming Wang
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Abstract

Background: Non-small cell lung cancer (NSCLC) is a malignant form of lung cancer, and its prognosis could be improved by identifying key therapeutic targets. Thus, this study investigates the potential role of F-box Only Protein 33 (FBXO33) in NSCLC.

Methods: The expression levels of FBXO33 in NSCLC were determined using University of Alabama at Birmingham Cancer Data Analysis Portal (UALCAN) prediction, and its correlation with overall survival (OS) was analyzed via Kaplan-Meier survival analysis. These results were validated through quantitative polymerase chain reaction (qPCR), western blot (WB), and immunofluorescence (IF). We modulated FBXO33 expression by overexpression or knockdown and analyzed its effects on cell growth, proliferation, migration, invasion, and stemness characteristics in NSCLC cell lines. Additionally, the interaction between FBXO33 and Myelocytomatosis (Myc) and its impact on Myc ubiquitination were examined. An in vivo NSCLC xenograft model was used to corroborate the in vivo experimental results.

Results: The study found an inverse correlation between FBXO33 expression in NSCLC and OS. Lower FBXO33 expression enhanced the growth, proliferation, migration, invasion, and stemness characteristics of NSCLC cell lines. FBXO33 interacted with Myc to promote its ubiquitination and subsequent degradation, which suppressed NSCLC development.

Conclusion: FBXO33 is expressed at low levels in NSCLC and correlates with lower OS. Overexpression of FBXO33 promotes Myc ubiquitination and degradation and inhibits tumor cell proliferation, migration and stemness characteristics, thereby impeding NSCLC progression.

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泛素 E3 连接酶 FBXO33 通过促进 Myc 的泛素化和降解抑制非小细胞肺癌的干细胞样特性和转移。
背景:非小细胞肺癌(NSCLC)是一种恶性肺癌:非小细胞肺癌(NSCLC)是肺癌的一种恶性形式,通过确定关键治疗靶点可改善其预后。因此,本研究探讨了 F-box Only Protein 33(FBXO33)在 NSCLC 中的潜在作用:方法:利用阿拉巴马大学伯明翰分校癌症数据分析门户网站(UALCAN)预测确定了FBXO33在NSCLC中的表达水平,并通过Kaplan-Meier生存分析法分析了其与总生存期(OS)的相关性。这些结果通过定量聚合酶链反应(qPCR)、免疫印迹(WB)和免疫荧光(IF)进行了验证。我们通过过表达或敲除调节了 FBXO33 的表达,并分析了它对 NSCLC 细胞系的细胞生长、增殖、迁移、侵袭和干性特征的影响。此外,还研究了FBXO33与骨髓细胞瘤(Myc)之间的相互作用及其对Myc泛素化的影响。为了证实体内实验结果,研究人员使用了一个体内 NSCLC 异种移植模型:研究发现,FBXO33在NSCLC中的表达与OS呈反相关。较低的 FBXO33 表达会增强 NSCLC 细胞系的生长、增殖、迁移、侵袭和干性特征。FBXO33与Myc相互作用,促进其泛素化并随后降解,从而抑制了NSCLC的发展:结论:FBXO33在NSCLC中低水平表达,并与较低的OS相关。结论:FBXO33在NSCLC中低水平表达,并与较低的OS相关。过表达FBXO33可促进Myc泛素化和降解,抑制肿瘤细胞的增殖、迁移和干性特征,从而阻碍NSCLC的进展。
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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