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细胞周期蛋白依赖性激酶抑制剂1B在人类癌症中的致癌作用的泛癌分析。

A pan-cancer analysis for the oncogenic role of cyclin-dependent kinase inhibitor 1B in human cancers.

作者信息

Huang Hao, Qiu Duoliang, Zhou Zhengyang, Wu Biaobiao, Shao Lening, Pu Yuwei, He Tengfei, Wu Yongyou, Cui Dawei, Zhong Fengyun

机构信息

Department of General Surgery, The Second Affiliated Hospital of Soochow University, Suzhou, China.

The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.

出版信息

Discov Oncol. 2023 Jul 11;14(1):126. doi: 10.1007/s12672-023-00746-8.

Abstract

BACKGROUND

Human health and life are threatened by cancer with high morbidity and mortality worldwide. In many experiments, CDKN1B level is associated with cancer risk, Nevertheless, no pan-cancer analysis has been conducted on CDKN1B in human cancers.

METHODS

With the help of bioinformatics, a pan-cancer analysis was conducted on the expression levels of CDKN1B in cancer tissues and adjacent tissues from the TCGA, CPTAC and GEO databases. The CDKN1B expression levels in tumor patients was further validated using immunohistochemistry (IHC) and quantitative real-time PCR.

RESULTS

In the study, we first investigated the cancer-related roles of CDKN1B's in 40 tumors with malignancy. The CDKN1B gene encodes the p27 protein, which can block the production cyclin-dependent kinase (CDK), which is obviously related to the function and survival of cancer cells and alters the prognosis of cancer patients. Furthermore, CDKN1B function requires both protein processing and RNA metabolism. Additionally, the elevated expression of the CDKN1B gene and protein was validated in several cancer tissues from the patients.

CONCLUSIONS

These results showed that the levels of CDKN1B were considerably different in a number of cancer tissues, offering a potential future target for cancer therapy.

摘要

背景

癌症在全球范围内具有高发病率和死亡率,威胁着人类健康和生命。在许多实验中,CDKN1B水平与癌症风险相关,然而,尚未对人类癌症中的CDKN1B进行泛癌分析。

方法

借助生物信息学,对来自TCGA、CPTAC和GEO数据库的癌组织和相邻组织中CDKN1B的表达水平进行了泛癌分析。使用免疫组织化学(IHC)和定量实时PCR进一步验证了肿瘤患者中CDKN1B的表达水平。

结果

在本研究中,我们首先研究了CDKN1B在40种恶性肿瘤中的癌症相关作用。CDKN1B基因编码p27蛋白,该蛋白可阻断细胞周期蛋白依赖性激酶(CDK)的产生,这显然与癌细胞的功能和存活相关,并改变癌症患者的预后。此外,CDKN1B的功能需要蛋白质加工和RNA代谢。此外,在患者的几种癌组织中验证了CDKN1B基因和蛋白的表达升高。

结论

这些结果表明,CDKN1B水平在许多癌组织中存在显著差异,为未来的癌症治疗提供了潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf44/10335976/67fcef02bdc4/12672_2023_746_Fig1_HTML.jpg

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