Intelligent Molecular Discovery Laboratory, Department of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, 77054, USA.
Department of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Sci Rep. 2022 Feb 15;12(1):2478. doi: 10.1038/s41598-022-06451-w.
The ubiquitination of SKP2, an oncoprotein, is controlled by its E3 ligases, including APC/C and deubiquitinases such as USP10. We identified a two-gene signature for the ubiquitination of SKP2, consisting of the copy number of FZR1 compared to the copy number of USP10. The signature reflects the level of SKP2 activity, stratifying BC patients into two groups with significantly different protein levels of SKP2 ubiquitination substrate p27 (t-test p < 0.01) and recapitulating the expression patterns of SKP2 between tumor and normal tissue (Spearman's ρ = 0.39.) The signature is also highly associated with clinical outcome in luminal BC but not other subtypes, characterizing patients into two groups with significantly different overall survival times (log-rank p = 0.006). In addition, it is dramatically associated with tumor grade (Chi-squared p = 6.7 × 10), stage (Chi-squared p = 1.6 × 10), and the number of positive lymph nodes (negative binomial regression coefficient p = 2.0 × 10). Our study provides a rationale for targeting the SKP2 ubiquitination pathway in luminal BC and for further investigation of the use of ubiquitinase/deubiquitinase genes as prognosis and treatment biomarkers.
SKP2 是一种癌蛋白,其泛素化受其 E3 连接酶(包括 APC/C 和去泛素化酶如 USP10)控制。我们确定了 SKP2 泛素化的两个基因特征,由 FZR1 的拷贝数与 USP10 的拷贝数之比组成。该特征反映了 SKP2 活性的水平,将 BC 患者分为两组,SKP2 泛素化底物 p27 的蛋白水平有显著差异(t 检验 p < 0.01),并再现了肿瘤和正常组织之间的 SKP2 表达模式(Spearman's ρ = 0.39)。该特征与 luminal BC 的临床结局高度相关,但与其他亚型无关,将患者分为两组,总生存时间有显著差异(对数秩检验 p = 0.006)。此外,它与肿瘤分级(卡方检验 p = 6.7×10)、分期(卡方检验 p = 1.6×10)和阳性淋巴结数量(负二项回归系数 p = 2.0×10)显著相关。我们的研究为在 luminal BC 中靶向 SKP2 泛素化途径提供了依据,并进一步探讨了泛素酶/去泛素化酶基因作为预后和治疗生物标志物的用途。