Huang Shujun, Xu Wayne, Hu Pingzhao, Lakowski Ted M
College of Pharmacy, University of Manitoba, Winnipeg, MB R3E 0T5, Canada. huangs12@myumanitoba.
College of Pharmacy, University of Manitoba, Winnipeg, MB R3E 0T5, Canada.
Cancers (Basel). 2019 Apr 10;11(4):507. doi: 10.3390/cancers11040507.
Different breast cancer (BC) subtypes have unique gene expression patterns, but their regulatory mechanisms have yet to be fully elucidated. We hypothesized that the top upregulated (Yin) and downregulated (Yang) genes determine the fate of cancer cells. To reveal the regulatory determinants of these Yin and Yang genes in different BC subtypes, we developed a lasso regression model integrating DNA methylation (DM), copy number variation (CNV) and microRNA (miRNA) expression of 391 BC patients, coupled with miRNA-target interactions and transcription factor (TF) binding sites. A total of 25, 20, 15 and 24 key regulators were identified for luminal A, luminal B, Her2-enriched, and triple negative (TN) subtypes, respectively. Many of the 24 TN regulators were found to regulate the PPARA and FOXM1 pathways. The Yin Yang gene expression mean ratio (YMR) and combined risk score (CRS) signatures built with either the targets of or the TN regulators were associated with the BC patients' survival. Previously, we identified FOXM1 and PPARA as the top Yin and Yang pathways in TN, respectively. These two pathways and their regulators could be further explored experimentally, which might help to identify potential therapeutic targets for TN.
不同的乳腺癌(BC)亚型具有独特的基因表达模式,但其调控机制尚未完全阐明。我们推测上调程度最高的(阴)基因和下调程度最高的(阳)基因决定癌细胞的命运。为了揭示这些阴阳基因在不同BC亚型中的调控决定因素,我们开发了一种套索回归模型,该模型整合了391例BC患者的DNA甲基化(DM)、拷贝数变异(CNV)和微小RNA(miRNA)表达,并结合了miRNA-靶标相互作用和转录因子(TF)结合位点。分别为腔面A型、腔面B型、人表皮生长因子受体2(Her2)富集型和三阴性(TN)亚型鉴定出25个、20个、15个和24个关键调节因子。发现24个TN调节因子中的许多可调节过氧化物酶体增殖物激活受体α(PPARA)和叉头框蛋白M1(FOXM1)信号通路。用TN调节因子的靶标构建的阴阳基因表达平均比值(YMR)和综合风险评分(CRS)特征与BC患者的生存相关。此前,我们分别将FOXM1和PPARA鉴定为TN中最主要的阴阳信号通路。这两条信号通路及其调节因子可进一步进行实验探索,这可能有助于确定TN的潜在治疗靶点。