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CBX3与EGFR或RAC1在人类癌症中的共扩增得到了这些基因间保守遗传相互作用的证实。

Co-amplification of CBX3 with EGFR or RAC1 in human cancers corroborated by a conserved genetic interaction among the genes.

作者信息

Bosso Giuseppe, Cipressa Francesca, Tullo Liliana, Cenci Giovanni

机构信息

Department of Biology and Biotechnology "C. Darwin", Sapienza Università di Roma, Rome, Italy.

Telomeres and Telomerase Group, Molecular Oncology Program, Spanish National Cancer Centre (CNIO), Melchor Fernández Almagro 3, Madrid, E-28029, Spain.

出版信息

Cell Death Discov. 2023 Aug 26;9(1):317. doi: 10.1038/s41420-023-01598-5.

Abstract

Chromobox Protein 3 (CBX3) overexpression is a common event occurring in cancer, promotes cancer cell proliferation and represents a poor prognosis marker in a plethora of human cancers. Here we describe that a wide spectrum of human cancers harbors a co-amplification of CBX3 gene with either EGFR or RAC1, which yields a statistically significant increase of both mRNA and protein levels of CBX3, EGFR and RAC1. We also reveal that the simultaneous overexpression of CBX3, RAC1 and EGFR gene products correlates with a worse prognosis compared to the condition when CBX3, RAC1 and EGFR are singularly upregulated. Furthermore, we also show that a co-occurrence of low-grade amplification, in addition to high-grade amplification, between CBX3 and EGFR or RAC1 is associated with a reduced patient lifespan. Finally, we find that CBX3 and RAC1/EGFR genetically interact in the model organism Drosophila melanogaster, suggesting that the simultaneous overexpression as well as well the co-occurrence of high- or low-grade copy number alterations in these genes is not accidental and could reflect evolutionarily conserved functional relationships.

摘要

染色质盒蛋白3(CBX3)过表达是癌症中常见的事件,可促进癌细胞增殖,并且在多种人类癌症中是预后不良的标志物。在此我们描述,多种人类癌症中存在CBX3基因与表皮生长因子受体(EGFR)或RAC1的共扩增,这导致CBX3、EGFR和RAC1的mRNA和蛋白质水平在统计学上显著增加。我们还揭示,与CBX3、RAC1和EGFR单独上调的情况相比,CBX3、RAC1和EGFR基因产物的同时过表达与更差的预后相关。此外,我们还表明,除了高级别扩增外,CBX3与EGFR或RAC1之间低级别扩增的同时出现与患者寿命缩短有关。最后,我们发现在模式生物黑腹果蝇中CBX3与RAC1/EGFR存在基因相互作用,这表明这些基因的同时过表达以及高或低级别拷贝数改变的同时出现并非偶然,可能反映了进化上保守的功能关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/273e/10460438/37187ba40b4a/41420_2023_1598_Fig1_HTML.jpg

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