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乳腺癌中8p11.23扩增:分子特征、预后及靶向治疗

8p11.23 Amplification in Breast Cancer: Molecular Characteristics, Prognosis and Targeted Therapy.

作者信息

Voutsadakis Ioannis A

机构信息

Algoma District Cancer Program, Sault Area Hospital, 750 Great Northern Road, Sault Ste Marie, ON P6B 0A8, Canada.

Section of Internal Medicine, Division of Clinical Sciences, Northern Ontario School of Medicine, Sudbury, ON P3E 2C6, Canada.

出版信息

J Clin Med. 2020 Sep 24;9(10):3079. doi: 10.3390/jcm9103079.

Abstract

BACKGROUND

Amplification of the locus 8p11.23 has been observed in cancer and genes of this locus, including ZNF703 (Zinc finger protein 703), NSD3 (Nuclear receptor binding SET domain protein 3) and FGFR1 (Fibroblast growth factor receptor 1), have been put forward as dominant oncogenes conferring pathophysiologic benefit in cancers with amplifications. However, there is no consensus on the importance of each of them or any other genes of the amplicon or even a consensus on which genes are part of the amplicon.

METHODS

Publicly available data were used to characterize the locus amplified at 8p11.23 and derive information on each of the genes and roles as oncogenes. The frequency of the amplifications in the locus was examined in the cBioportal platform, and expression levels of the amplicon genes in amplified cases were derived from genomic studies reported in the platform. Examination of the influence of mRNA expressions of each gene of the locus for Recurrence-free survival in breast cancer was performed using K-M plotter.

RESULTS

The 8p11.23 amplicon is present in higher frequency in squamous cell lung carcinomas, breast cancers and bladder carcinomas and is only rarely observed in other cancers. The most frequently amplified genes within the amplicon vary between different types of cancers. In breast cancer, amplified cases are most commonly of the luminal B type. Amplified genes are not always over-expressed and there is a low correlation of amplification with over-expression in amplicon genes with variation between genes. The presence of the amplicon does not influence the aneuploidy score or the tumor mutation burden of breast cancers. Regarding prognosis, the two genes of the amplicon whose mRNA hyper-expression portends adverse relapse-free survival in breast cancer are EIF4EBP1 (Eukaryotic transcription initiation factor 4E binding protein 1) and LSM1 (LSM1 homolog, mRNA degradation associated).

CONCLUSION

Besides the previously proposed genes to play a role as dominant oncogenes in the 8p11.23 cancer amplified locus, other genes may also be important in breast cancer based on the high correlation of their amplification and mRNA expression and adverse prognosis conferred by over-expression, consistent with an oncogenic role.

摘要

背景

在癌症中已观察到8p11.23位点的扩增,该位点的基因,包括ZNF703(锌指蛋白703)、NSD3(核受体结合SET结构域蛋白3)和FGFR1(成纤维细胞生长因子受体1),已被提出作为在扩增的癌症中赋予病理生理益处的主要癌基因。然而,对于它们中每一个或扩增子的任何其他基因的重要性,甚至对于哪些基因是扩增子的一部分,都没有达成共识。

方法

使用公开可用的数据来表征在8p11.23扩增的位点,并获取每个基因的信息及其作为癌基因的作用。在cBioportal平台上检查该位点扩增的频率,并从该平台报道的基因组研究中获取扩增病例中扩增子基因的表达水平。使用K-M绘图仪检查该位点每个基因的mRNA表达对乳腺癌无复发生存的影响。

结果

8p11.23扩增子在肺鳞状细胞癌、乳腺癌和膀胱癌中出现的频率较高,而在其他癌症中很少观察到。扩增子内最常扩增的基因在不同类型的癌症中有所不同。在乳腺癌中,扩增病例最常见的是管腔B型。扩增的基因并不总是过度表达,扩增与扩增子基因中过度表达之间的相关性较低,且基因之间存在差异。扩增子的存在并不影响乳腺癌的非整倍体评分或肿瘤突变负担。关于预后,扩增子中其mRNA高表达预示乳腺癌无复发生存不良的两个基因是EIF4EBP1(真核转录起始因子4E结合蛋白1)和LSM1(LSM1同源物,与mRNA降解相关)。

结论

除了先前提出的在8p11.23癌症扩增位点中起主要癌基因作用的基因外,基于其扩增与mRNA表达的高度相关性以及过度表达所赋予的不良预后,其他基因在乳腺癌中可能也很重要,这与致癌作用一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1a9/7598661/f964df67eebc/jcm-09-03079-g001.jpg

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