Department of Thyroid Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Department of Urology, Fenyang Hospital of Shanxi Province, Lüliang, Shanxi, China.
Sci Rep. 2024 Sep 29;14(1):22574. doi: 10.1038/s41598-024-73455-z.
Emerging evidence have demonstrated that F-box only protein 2 (FBXO2) is intimately associated with malignant tumor development and occurrence. However, neither the functions nor the molecular mechanisms underlying FBXO2 have been determined in the papillary thyroid carcinoma (PTC). The quantitative real-time PCR (qRT-PCR), western blotting and immunohistochemistry were carried out to detect the FBXO2 expression in PTC tissues. CCK-8 assay, EdU assay and flow cytometry were used to assess cell proliferation, cell cycle and apoptosis. The trans-well assay was conducted to determine the cell invasiveness. The effect of FBXO2 on PTC cell proliferation in vivo was observed through a subcutaneous tumor formation experiment in nude mice. Immunoprecipitation were conducted to detect the interaction between FBXO2 and p53. The ubiquitination assays were conducted to assess the regulation of p53 ubiquitination by FBXO2. FBXO2 was overexpressed in both PTC tissues and cell lines. FBXO2 expression positively correlated with PTC tumor size, lymphatic metastasis, and extramembranous invasion. Furthermore, silencing FBXO2 inhibited PTC cell proliferation and promoted apoptosis. The overexpression of FBXO2 significantly promotes PTC cell proliferation. Mechanistic studies revealed that FBXO2 could directly bind to p53 and promote its ubiquitination degradation. Knockdown of p53 partially reversed the progression arrest induced by FBXO2 Knockdown in PTC cells. FBXO2 knockdown inhibited PTC cell proliferation and promoted apoptosis by targeting p53 for ubiquitination and degradation. This process represents a research foundation for its diagnostic and therapeutic applications.
越来越多的证据表明,F-box 仅蛋白 2(FBXO2)与恶性肿瘤的发生和发展密切相关。然而,在甲状腺乳头状癌(PTC)中,FBXO2 的功能及其分子机制尚不清楚。本研究通过实时定量 PCR(qRT-PCR)、蛋白质印迹和免疫组织化学检测 FBXO2 在 PTC 组织中的表达。CCK-8 检测、EdU 检测和流式细胞术检测细胞增殖、细胞周期和细胞凋亡。Transwell 检测用于检测细胞侵袭能力。通过裸鼠皮下肿瘤形成实验观察 FBXO2 对 PTC 细胞体内增殖的影响。免疫沉淀检测 FBXO2 与 p53 的相互作用。泛素化测定评估 FBXO2 对 p53 泛素化的调节。FBXO2 在 PTC 组织和细胞系中均过表达。FBXO2 的表达与 PTC 肿瘤大小、淋巴转移和膜外浸润呈正相关。此外,沉默 FBXO2 抑制 PTC 细胞增殖并促进细胞凋亡。FBXO2 的过表达显著促进 PTC 细胞增殖。机制研究表明,FBXO2 可以直接与 p53 结合并促进其泛素化降解。在 PTC 细胞中敲低 p53 部分逆转了 FBXO2 敲低引起的进展停滞。FBXO2 敲低通过靶向 p53 进行泛素化和降解抑制 PTC 细胞增殖并促进细胞凋亡。这一过程为其诊断和治疗应用提供了研究基础。