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MCM2 - 7在透明细胞肾细胞癌中的作用:MCM7促进肿瘤细胞增殖。

MCM2-7 in Clear Cell Renal Cell Carcinoma: MCM7 Promotes Tumor Cell Proliferation.

作者信息

Zhang Junneng, Zhang Huanzong, Wang Yinghui, Wang Qingshui

机构信息

Laboratory Medicine Department, The Fifth Hospital of Xiamen, Xiamen, China.

Key Laboratory of Optoelectronic Science and Technology for Medicine of Ministry of Education, College of Life Sciences, Fujian Normal University, Fuzhou, China.

出版信息

Front Oncol. 2021 Dec 21;11:782755. doi: 10.3389/fonc.2021.782755. eCollection 2021.

Abstract

BACKGROUND

Clear cell renal cell carcinoma (ccRCC) accounts for 60-70% of renal cell carcinoma (RCC) cases. Finding more therapeutic targets for advanced ccRCC is an urgent mission. The minichromosome maintenance proteins 2-7 (MCM2-7) protein forms a stable heterohexamer and plays an important role in DNA replication in eukaryotic cells. In the study, we provide a comprehensive study of MCM2-7 genes expression and their potential roles in ccRCC.

METHODS

The expression and prognosis of the MCM2-7 genes in ccRCC were analyzed using data from TCGA, GEO and ArrayExpress. MCM2-7 related genes were identified by weighted co-expression network analysis (WGCNA) and Metascape. CancerSEA and GSEA were used to analyze the function of MCM2-7 genes in ccRCC. The gene effect scores (CERES) of MCM2-7, which reflects carcinogenic or tumor suppressor, were obtained from DepMap. We used clinical and expression data of MCM2-7 from the TCGA dataset and the LASSO Cox regression analysis to develop a risk score to predict survival of patients with ccRCC. The correlations between risk score and other clinical indicators such as gender, age and stage were also analyzed. Further validation of this risk score was engaged in another cohort, E-MTAB-1980 from the ArrayExpress dataset.

RESULTS

The mRNA and protein expression of MCM2-7 were increased in ccRCC compared with normal tissues. High MCM2, MCM4, MCM6 and MCM7 expression were associated with a poor prognosis of ccRCC patients. Functional enrichment analysis revealed that MCM2-7 might influence the progress of ccRCC by regulating the cell cycle. Knockdown of MCM7 can inhibit the proliferation of ccRCC cells. A two-gene risk score including MCM4 and MCM6 can predict overall survival (OS) of ccRCC patients. The risk score was successfully verified by further using Arrayexpress cohort.

CONCLUSION

We analyze MCM2-7 mRNA and protein levels in ccRCC. MCM7 is determined to promote tumor proliferation. Meanwhile, our study has determined a risk score model composed of MCM2-7 can predict the prognosis of ccRCC patients, which may help future treatment strategies.

摘要

背景

透明细胞肾细胞癌(ccRCC)占肾细胞癌(RCC)病例的60 - 70%。为晚期ccRCC寻找更多治疗靶点是一项紧迫任务。微小染色体维持蛋白2 - 7(MCM2 - 7)形成稳定的异源六聚体,在真核细胞的DNA复制中起重要作用。在本研究中,我们全面研究了MCM2 - 7基因在ccRCC中的表达及其潜在作用。

方法

利用来自TCGA、GEO和ArrayExpress的数据,分析MCM2 - 7基因在ccRCC中的表达和预后。通过加权共表达网络分析(WGCNA)和Metascape鉴定MCM2 - 7相关基因。使用CancerSEA和GSEA分析MCM2 - 7基因在ccRCC中的功能。从DepMap获得反映致癌或抑癌作用的MCM2 - 7基因效应评分(CERES)。我们利用TCGA数据集的MCM2 - 7临床和表达数据以及LASSO Cox回归分析来建立一个风险评分,以预测ccRCC患者的生存情况。还分析了风险评分与性别、年龄和分期等其他临床指标之间的相关性。在另一个队列(来自ArrayExpress数据集的E - MTAB - 1980)中对该风险评分进行了进一步验证。

结果

与正常组织相比,ccRCC中MCM2 - 7的mRNA和蛋白表达增加。MCM2、MCM4、MCM6和MCM7的高表达与ccRCC患者的不良预后相关。功能富集分析表明,MCM2 - 7可能通过调节细胞周期影响ccRCC的进展。敲低MCM7可抑制ccRCC细胞的增殖。一个包含MCM4和MCM6的双基因风险评分可以预测ccRCC患者的总生存期(OS)。通过进一步使用Arrayexpress队列成功验证了该风险评分。

结论

我们分析了ccRCC中MCM2 - 7的mRNA和蛋白水平。确定MCM7促进肿瘤增殖。同时,我们的研究确定了一个由MCM2 - 7组成的风险评分模型,可以预测ccRCC患者的预后,这可能有助于未来的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61df/8724441/7b0cc8c525f2/fonc-11-782755-g001.jpg

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