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C19orf10在肾透明细胞癌中的临床相关性及肿瘤促进功能

The Clinical Relevance and Tumor Promoting Function of C19orf10 in Kidney Renal Clear Cell Carcinoma.

作者信息

Lu Yanxin, Liao Ximian, Wang Tongyu, Hong Xiaowei, Li Zesong

机构信息

Guangdong Provincial Key Laboratory of Systems Biology and Synthetic Biology for Urogenital Tumors, Department of Urology, The First Affiliated Hospital of Shenzhen University, Shenzhen Second People's Hospital (Shenzhen Institute of Translational Medicine), Shenzhen, China.

Basic Medical Science Department, Zunyi Medical University, Zhuhai, China.

出版信息

Front Oncol. 2021 Sep 6;11:725959. doi: 10.3389/fonc.2021.725959. eCollection 2021.

Abstract

Kidney renal clear cell carcinoma (KIRC) is the most common primary renal neoplasms. Currently, there are few molecular indicators and therapeutic targets that can be used in diagnostic and prognostic assessment. In this study, we identified the C19orf10 expression in KIRC specimens and explored the diagnostic and prognostic value of C19orf10 in KIRC using TCGA and CPTAC database. Loss-of- and gain-of- function of C19orf10 was performed to investigate the roles of C19orf10 on KIRC cell viability, proliferation, migration and invasion CCK-8, Edu incorporation and Transwell assays respectively. C19orf10 was overexpressed in KIRC tissues and the elevated C19orf10 expression was closely associated with clinicopathological characteristics of KIRC including histological grade, TNM stage, metastatic status. Silencing C19orf10 significantly suppressed the viability, proliferation, migration and invasion ability, while overexpression of C19orf10 promoted the progression and malignant phenotype in KIRC cells. Furthermore, C19orf10 exerted its carcinogenic function by regulating ZO-1 and PTEN/Akt signaling pathway. Moreover, the Kaplan-Meier survival analysis, Cox regression analysis and receiver operating curve analysis showed that patients with C19orf10 overexpression have poor survival time. C19orf10 could discriminate KIRC patients with high-risk from low-risk. Taken together, C19orf10 contributes to KIRC development ZO-1 and PTEN/Akt signaling pathway and C19orf10 could serve as a potential diagnostic and prognostic candidate and therapeutic target of KIRC.

摘要

肾透明细胞癌(KIRC)是最常见的原发性肾肿瘤。目前,可用于诊断和预后评估的分子指标和治疗靶点很少。在本研究中,我们检测了KIRC标本中C19orf10的表达,并利用TCGA和CPTAC数据库探讨了C19orf10在KIRC中的诊断和预后价值。通过分别进行C19orf10的功能缺失和功能获得实验,利用CCK-8、Edu掺入和Transwell实验研究C19orf10对KIRC细胞活力、增殖、迁移和侵袭的作用。C19orf10在KIRC组织中过表达,C19orf10表达升高与KIRC的临床病理特征密切相关,包括组织学分级、TNM分期、转移状态。沉默C19orf10可显著抑制细胞活力、增殖、迁移和侵袭能力,而C19orf10过表达则促进KIRC细胞的进展和恶性表型。此外,C19orf10通过调节ZO-1和PTEN/Akt信号通路发挥致癌作用。此外,Kaplan-Meier生存分析、Cox回归分析和受试者工作特征曲线分析表明,C19orf10过表达的患者生存时间较差。C19orf10可区分高风险和低风险的KIRC患者。综上所述,C19orf10通过ZO-1和PTEN/Akt信号通路促进KIRC的发展,C19orf10可作为KIRC潜在的诊断、预后候选指标和治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc62/8451477/759fca877f4f/fonc-11-725959-g001.jpg

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