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BIRC5 的上调在食管鳞状细胞癌中起着重要作用。

Upregulation of BIRC5 plays essential role in esophageal squamous cell carcinoma.

机构信息

Department of Medical Oncology, Second Affiliated Hospital of Guangxi Medical University, 166 DaxueXi Road, Nanning, Guangxi Zhuang Autonomous Region, 530021, P. R. China.

Department of Medical Oncology, First Affiliated Hospital of Guangxi Medical University, 6 Shuangyong Road, Nanning, Guangxi Zhuang Autonomous Region, 530021, P. R. China.

出版信息

Math Biosci Eng. 2021 Aug 20;18(5):6941-6960. doi: 10.3934/mbe.2021345.

Abstract

BACKGROUND

Esophageal squamous cell carcinoma (ESCC) is one of the most common cancers in the world, the detection and prognosis of which are still unsatisfactory. Thus, it is essential to explore the factors that may identify ESCC and evaluate the prognosis of ESCC patients.

RESULTS

Both protein and mRNA expression levels of BIRC5 are upregulated in ESCC group rather than non-ESCC group (standardized mean difference > 0). BIRC5 mRNA expression is related to the age, tumor location, lymph node stage and clinical stage of ESCC patients (p < 0.05). BIRC5 expression makes it feasible to distinguish ESCC from non-ESCC (area under the curve > 0.9), and its high expression is related to poor prognosis of ESCC patients (restrictive survival time difference = -0.036, p < 0.05). BIRC5 may play an important role in ESCC by influencing the cell cycle pathway, and CDK1, MAD2L and CDC20 may be the hub genes of this pathway. The transcription factors-MAZ and TFPD1 -are likely to regulate the transcription of BIRC5, which may be one of the factors for the high expression of BIRC5 in ESCC.

CONCLUSIONS

The current study shows that upregulation of BIRC5 may have essential clinical value in ESCC, and contributes to the understanding of the pathogenesis of ESCC.

摘要

背景

食管鳞状细胞癌(ESCC)是世界上最常见的癌症之一,其检测和预后仍不理想。因此,探索可能识别 ESCC 的因素并评估 ESCC 患者的预后至关重要。

结果

ESCC 组的 BIRC5 蛋白和 mRNA 表达水平均高于非 ESCC 组(标准化均数差>0)。BIRC5 mRNA 表达与 ESCC 患者的年龄、肿瘤位置、淋巴结分期和临床分期相关(p<0.05)。BIRC5 表达可区分 ESCC 和非 ESCC(曲线下面积>0.9),其高表达与 ESCC 患者预后不良相关(限制生存时间差异=-0.036,p<0.05)。BIRC5 可能通过影响细胞周期途径在 ESCC 中发挥重要作用,CDK1、MAD2L 和 CDC20 可能是该途径的枢纽基因。转录因子-MAZ 和 TFPD1 可能调节 BIRC5 的转录,这可能是 ESCC 中 BIRC5 高表达的因素之一。

结论

本研究表明,BIRC5 的上调在 ESCC 中可能具有重要的临床价值,并有助于了解 ESCC 的发病机制。

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