Yang Jiawen, de Oliveira Pessoa Diogo, Ryniawec John M, Coope Matthew R, Buster Daniel W, Loertscher Emily, Wang Mengdie, Chen Chen, Cress Anne E, Rogers Gregory C, Padi Megha
Department of Molecular and Cellular Biology, University of Arizona, Tucson, AZ 85721, USA.
Department of Cellular and Molecular Medicine, University of Arizona Cancer Center, University of Arizona, Tucson, AZ 85724, USA.
bioRxiv. 2025 May 12:2025.05.10.653266. doi: 10.1101/2025.05.10.653266.
Chromosomal instability (CIN) is a hallmark of prostate cancer that strongly correlates with metastatic burden and appears prominently in both primary cancer and metastatic disease. Low Gleason score primary prostate tumors display pervasive centrosome loss, a known mechanistic driver of CIN, that disrupts normal spindle assembly and increases mitotic errors. Previously, we found that transient depletion of centrosomes in immortalized, non-tumorigenic prostate epithelial cells (PrEC) induced a burst of CIN, generating cell lines capable of forming xenograft tumors. Here, we use a multi-omics approach to identify the oncogenic alterations caused by transient centrosome loss. By integrating genomic and transcriptomic data of the prostate lines, we identified a consensus set of focal copy-number variations (CNVs) induced by centrosome loss in cultured cells that are also detectable within a subset of samples from a prostate cancer patient cohort. Using this CNV signature, we were able to derive a unique transcriptomic signature from prostate cancer patient samples that showed strong predictive value for adverse clinical outcomes. In summary, our experimental system uses centrosome loss to promote a punctuated burst of genomic crisis that is characteristic of genome evolution during prostate cancer progression. Consequently, this prostate cancer model produced recurrent structural variations that are detectable in patient samples and associate with worse outcomes.
染色体不稳定(CIN)是前列腺癌的一个标志,与转移负担密切相关,在原发性癌症和转移性疾病中均显著出现。低Gleason评分的原发性前列腺肿瘤表现出普遍的中心体缺失,这是一种已知的CIN机制驱动因素,会破坏正常的纺锤体组装并增加有丝分裂错误。此前,我们发现永生化、非致瘤性前列腺上皮细胞(PrEC)中中心体的短暂缺失会引发一阵CIN,从而产生能够形成异种移植肿瘤的细胞系。在这里,我们使用多组学方法来识别由中心体短暂缺失引起的致癌改变。通过整合前列腺细胞系的基因组和转录组数据,我们确定了一组由培养细胞中中心体缺失诱导的一致性局灶性拷贝数变异(CNV),这些变异在前列腺癌患者队列的一部分样本中也可检测到。利用这个CNV特征,我们能够从前列腺癌患者样本中得出一个独特的转录组特征,该特征对不良临床结果具有很强的预测价值。总之,我们的实验系统利用中心体缺失来促进一阵基因组危机,这是前列腺癌进展过程中基因组进化的特征。因此,这个前列腺癌模型产生了在患者样本中可检测到的复发性结构变异,并与更差的结果相关。