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小分子核仁RNA SNORD6通过加速E6介导的p53降解促进宫颈癌进展。

SNORD6 promotes cervical cancer progression by accelerating E6-mediated p53 degradation.

作者信息

Li Qianhui, Xie Bumin, Chen Xi, Lu Bingfeng, Chen Shuo, Sheng Xiujie, Zhao Yang

机构信息

Department of Obstetrics and Gynecology, Department of Gynecologic Oncology Research Office, Guangzhou Key Laboratory of Targeted Therapy for Gynecologic Oncology, Guangdong Provincial Key Laboratory of Major Obstetric Diseases, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, 510150, China.

出版信息

Cell Death Discov. 2023 Jun 27;9(1):192. doi: 10.1038/s41420-023-01488-w.

Abstract

Small nucleolar RNAs (snoRNAs) are a class of non-coding RNAs widely distributed in eukaryotic nucleoli. In recent years, studies have revealed that snoRNAs can also participate in the occurrence and development of malignant tumors through different pathways. Cervical cancer is one of the most common malignant tumors of the female reproductive system, and the high-risk HPV virus infection is its main pathogenic mechanism. However, the outcomes in different patients with malignant tumors vary, indicating that other factors might affect the pathogenic process of cervical cancer. In this study, we screened the poor prognosis indicator SNORD6 from the TCGA database to find the snoRNA that affects the disease outcome during the pathogenesis of cervical cancer. We discovered that SNORD6 expression in cervical cancer tissues was higher than that in normal cervical tissues. Cell phenotype experiments revealed that the knockdown of SNORD6 retarded cell proliferation and plate clone formation. Furthermore, G1-S phase cell cycle arrest was induced, DNA synthesis was decreased, cell migration and invasion were reduced, while the level of apoptosis increased, whereas the opposite results were obtained after SNORD6 overexpression. Moreover, after intratumoral injection of ASO-SNORD6, the tumor growth rate slowed down, and the tumor volume decreased compared with the control group. In the mechanism study, we found that SNORD6 concurrently acted as a binding "hub" to promote the formation of the tumor suppressor protein p53 degradation complex E6-E6AP-p53. This reaction enhanced the ubiquitination and degradation of p53, thus influenced the regulation of p53 activities in the cell cycle and apoptosis. This study preliminarily clarified the biological role and specific mechanism of SNORD6 in the occurrence of cervical cancer, broadening the basic theoretical research of ovarian cancer and may provide a new perspective on the diagnosis and treatment of cervical cancer.

摘要

小核仁RNA(snoRNAs)是一类广泛分布于真核生物核仁中的非编码RNA。近年来,研究表明snoRNAs也可通过不同途径参与恶性肿瘤的发生发展。宫颈癌是女性生殖系统最常见的恶性肿瘤之一,高危型人乳头瘤病毒(HPV)感染是其主要致病机制。然而,不同恶性肿瘤患者的预后各不相同,这表明其他因素可能影响宫颈癌的致病过程。在本研究中,我们从TCGA数据库中筛选出预后不良指标SNORD6,以寻找在宫颈癌发病机制中影响疾病预后的snoRNA。我们发现宫颈癌组织中SNORD6的表达高于正常宫颈组织。细胞表型实验表明,敲低SNORD6可抑制细胞增殖和平板克隆形成。此外,诱导G1-S期细胞周期阻滞,DNA合成减少,细胞迁移和侵袭能力降低,而细胞凋亡水平增加,而SNORD6过表达后则得到相反的结果。此外,瘤内注射ASO-SNORD6后,与对照组相比,肿瘤生长速度减慢,肿瘤体积减小。在机制研究中,我们发现SNORD6同时作为一个结合“枢纽”,促进肿瘤抑制蛋白p53降解复合物E6-E6AP-p53的形成。该反应增强了p53的泛素化和降解,从而影响了p53在细胞周期和凋亡中的活性调控。本研究初步阐明了SNORD6在宫颈癌发生中的生物学作用和具体机制,拓宽了卵巢癌的基础理论研究,可能为宫颈癌的诊断和治疗提供新的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a599/10300194/3e213adbe5af/41420_2023_1488_Fig1_HTML.jpg

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