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分选连接蛋白5通过调节FBW7来控制头颈部鳞状细胞癌的进展。

Sorting Nexin 5 Controls Head and Neck Squamous Cell Carcinoma Progression by Modulating FBW7.

作者信息

Cai Jinyang, Sun Ming, Hu Bin, Windle Brad, Ge Xin, Li Guoping, Sun Yue

机构信息

Philips Institute for Oral Health Research, School of Dentistry and Massey Cancer Center, Virginia Commonwealth University, Richmond, VA 23298, USA.

Cancer Mouse Models Developing Shared Resource Core, Virginia Commonwealth University, Richmond, VA 23298, USA.

出版信息

J Cancer. 2019 Jun 2;10(13):2942-2952. doi: 10.7150/jca.31055. eCollection 2019.

Abstract

Head and neck squamous cell carcinoma (HNSCC) is the sixth most prevalent cancer worldwide. Long-term survival rates in patients with HNSCC have not increased significantly in the past 30 years. Therefore, looking for novel molecular targets that control HNSCC progression is urgently required to improve the treatment of HNSCC. Here, we identified Sorting Nexin 5 (SNX5) as a new regulator that plays an oncogenic function in HNSCC progression. Analyzing HNSCC patients' data from the Cancer Genome Atlas (TCGA) indicates that the expression levels of SNX5 in HNSCC are significantly elevated compared to normal tissues. Furthermore, higher SNX5 expression correlates with a worse prognosis for HNSCC patients. These results suggest that SNX5 has an oncogenic role. Consistently, loss of SNX5 in HNSCC cells dramatically reduces colony formation and significantly decreases tumor growth in xenograft mouse models. SNX5 interacts with the tumor suppressor F-box/WD repeat-containing protein 7 (FBW7), an E3 ubiquitin ligase that mediates ubiquitination and degradation of oncoproteins such as c-Myc, NOTCH1, and Cyclin E1. By interacting with FBW7, SNX5 inhibits FBW7-mediated oncoproteins ubiquitination. In this way, SNX5 decreases the FBW7-mediated oncoproteins degradation to promote HNSCC progression.

摘要

头颈部鳞状细胞癌(HNSCC)是全球第六大常见癌症。在过去30年中,HNSCC患者的长期生存率并未显著提高。因此,迫切需要寻找控制HNSCC进展的新分子靶点,以改善HNSCC的治疗。在此,我们确定分选连接蛋白5(SNX5)是一种在HNSCC进展中发挥致癌作用的新调节因子。分析来自癌症基因组图谱(TCGA)的HNSCC患者数据表明,与正常组织相比,HNSCC中SNX5的表达水平显著升高。此外,较高的SNX5表达与HNSCC患者的较差预后相关。这些结果表明SNX5具有致癌作用。一致地,HNSCC细胞中SNX5的缺失显著减少集落形成,并显著降低异种移植小鼠模型中的肿瘤生长。SNX5与肿瘤抑制因子含F盒/ WD重复蛋白7(FBW7)相互作用,FBW7是一种E3泛素连接酶,介导c-Myc、NOTCH1和细胞周期蛋白E1等癌蛋白的泛素化和降解。通过与FBW7相互作用,SNX5抑制FBW7介导的癌蛋白泛素化。通过这种方式,SNX5减少FBW7介导的癌蛋白降解,以促进HNSCC进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d64/6590026/d6998faa75b9/jcav10p2942g001.jpg

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