Mechanistic study of NUPR1 in bladder cancer development through transcriptional regulation of CCR2.

IF 4.5 2区 生物学 Q2 CELL BIOLOGY Journal of Cellular Physiology Pub Date : 2024-08-16 DOI:10.1002/jcp.31412
Zebin Shi, Yuanyuan Mi, Li Zhang, Wenxu Zhang, Wei Zhang, Xiaokai Shi, Shenglin Gao, Li Zuo, Lifeng Zhang
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Abstract

Nuclear protein-1 (NUPR1) (also known as p8) is one of the genes associated with transcription factors that participate in various aspects of cancer initiation and development. However, the molecular mechanisms of NUPR1 in bladder cancer (BLCA) remain unclear. We conducted an analysis of the correlation between NUPR1 expression and related genes using the Gene Expression Omnibus (GEO) online database. We employed lentivirus-mediated small interfering RNA (siRNA) to knockdown the expression of NUPR1 in two human BLCA cell lines. In vitro experiments were conducted to validate the impact of NUPR1 interference on BLCA and the influence of NUPR1 on the transcription of chemokine receptor-2 (CCR2). Furthermore, transcription factors for CCR2 were predicted using the PROMO database. Co-immunoprecipitation (Co-IP) and immunofluorescence double staining were used to detect the binding between NUPR1 and CCAAT/enhancer binding protein γ (CEBPG). In vivo and in vitro experiments were conducted to validate that NUPR1 regulates CCR2 transcription through CEBPG. In vitro experiments indicate that the suppression of NUPR1 inhibited BLCA growth. Analysis of the GEO database revealed a positive correlation between the expression of NUPR1 and CCR2. Luciferase experiments confirmed that NUPR1 influences the transcription of CCR2. Online data indicates that CEBPG is a transcription factor for CCR2. Co-IP and immunofluorescence double staining confirmed binding between NUPR1 and CEBPG. Luciferase assays and chromatin immunoprecipitation (ChIP) demonstrate that CEBPG regulates the transcription of CCR2. Additionally, rescue experiments at the cellular level and animal experiments validated the aforementioned mechanism. NUPR1 promotes a promotional role in BLCA, and interference with NUPR1 can inhibit the proliferation and invasive abilities of BLCA. There was a correlation between the expressions of NUPR1 and CCR2, and NUPR1 binds with CEBPG in the cell nucleus. Transcriptional regulation of CCR2 by NUPR1 may be achieved through the involvement of CEBPG.

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NUPR1 通过 CCR2 的转录调控膀胱癌发展的机制研究。
核蛋白-1(NUPR1)(又称 p8)是与转录因子相关的基因之一,转录因子参与了癌症发生和发展的各个方面。然而,NUPR1 在膀胱癌(BLCA)中的分子机制仍不清楚。我们利用基因表达总库(GEO)在线数据库对 NUPR1 表达与相关基因之间的相关性进行了分析。我们采用慢病毒介导的小干扰 RNA(siRNA)来敲除两种人类 BLCA 细胞系中 NUPR1 的表达。体外实验验证了 NUPR1 干扰对 BLCA 的影响,以及 NUPR1 对趋化因子受体-2(CCR2)转录的影响。此外,还利用 PROMO 数据库预测了 CCR2 的转录因子。共免疫沉淀(Co-IP)和免疫荧光双重染色被用来检测NUPR1和CCAAT/增强子结合蛋白γ(CEBPG)之间的结合。体内和体外实验验证了 NUPR1 通过 CEBPG 调节 CCR2 的转录。体外实验表明,抑制 NUPR1 可抑制 BLCA 的生长。对 GEO 数据库的分析表明,NUPR1 和 CCR2 的表达呈正相关。荧光素酶实验证实 NUPR1 会影响 CCR2 的转录。在线数据表明 CEBPG 是 CCR2 的转录因子。Co-IP 和免疫荧光双重染色证实了 NUPR1 和 CEBPG 之间的结合。荧光素酶测定和染色质免疫沉淀(ChIP)证明 CEBPG 可调控 CCR2 的转录。此外,细胞水平的拯救实验和动物实验也验证了上述机制。NUPR1对BLCA有促进作用,干扰NUPR1可抑制BLCA的增殖和侵袭能力。NUPR1与CCR2的表达存在相关性,NUPR1与细胞核中的CEBPG结合。NUPR1对CCR2的转录调控可能是通过CEBPG的参与实现的。
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来源期刊
CiteScore
14.70
自引率
0.00%
发文量
256
审稿时长
1 months
期刊介绍: The Journal of Cellular Physiology publishes reports of high biological significance in areas of eukaryotic cell biology and physiology, focusing on those articles that adopt a molecular mechanistic approach to investigate cell structure and function. There is appreciation for the application of cellular, biochemical, molecular and in vivo genetic approaches, as well as the power of genomics, proteomics, bioinformatics and systems biology. In particular, the Journal encourages submission of high-interest papers investigating the genetic and epigenetic regulation of proliferation and phenotype as well as cell fate and lineage commitment by growth factors, cytokines and their cognate receptors and signal transduction pathways that influence the expression, integration and activities of these physiological mediators. Similarly, the Journal encourages submission of manuscripts exploring the regulation of growth and differentiation by cell adhesion molecules in addition to the interplay between these processes and those induced by growth factors and cytokines. Studies on the genes and processes that regulate cell cycle progression and phase transition in eukaryotic cells, and the mechanisms that determine whether cells enter quiescence, proliferate or undergo apoptosis are also welcomed. Submission of papers that address contributions of the extracellular matrix to cellular phenotypes and physiological control as well as regulatory mechanisms governing fertilization, embryogenesis, gametogenesis, cell fate, lineage commitment, differentiation, development and dynamic parameters of cell motility are encouraged. Finally, the investigation of stem cells and changes that differentiate cancer cells from normal cells including studies on the properties and functions of oncogenes and tumor suppressor genes will remain as one of the major interests of the Journal.
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