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非整倍体导致前列腺癌的致命进展。

Aneuploidy drives lethal progression in prostate cancer.

机构信息

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY 10065.

Department of Epidemiology, Harvard T. H. Chan School of Public Health, Boston, MA 02115.

出版信息

Proc Natl Acad Sci U S A. 2019 Jun 4;116(23):11390-11395. doi: 10.1073/pnas.1902645116. Epub 2019 May 13.

Abstract

Aneuploidy, defined as chromosome gains and losses, is a hallmark of cancer. However, compared with other tumor types, extensive aneuploidy is relatively rare in prostate cancer. Thus, whether numerical chromosome aberrations dictate disease progression in prostate cancer patients is not known. Here, we report the development of a method based on whole-transcriptome profiling that allowed us to identify chromosome-arm gains and losses in 333 primary prostate tumors. In two independent cohorts ( = 404) followed prospectively for metastases and prostate cancer-specific death for a median of 15 years, increasing extent of tumor aneuploidy as predicted from the tumor transcriptome was strongly associated with higher risk of lethal disease. The 23% of patients whose tumors had five or more predicted chromosome-arm alterations had 5.3 times higher odds of lethal cancer (95% confidence interval, 2.2 to 13.1) than those with the same Gleason score and no predicted aneuploidy. Aneuploidy was associated with lethality even among men with high-risk Gleason score 8-to-10 tumors. These results point to a key role of aneuploidy in driving aggressive disease in primary prostate cancer.

摘要

非整倍体,定义为染色体的增益和缺失,是癌症的一个标志。然而,与其他肿瘤类型相比,前列腺癌中广泛的非整倍体相对较少。因此,数值染色体异常是否决定前列腺癌患者的疾病进展尚不清楚。在这里,我们报告了一种基于全转录组谱分析的方法的发展,该方法允许我们在 333 个原发性前列腺肿瘤中识别染色体臂的增益和缺失。在两个独立的队列中(= 404),前瞻性地随访了中位时间为 15 年的转移和前列腺癌特异性死亡情况,从肿瘤转录组预测的肿瘤非整倍体程度的增加与致命疾病的风险增加强烈相关。在预测有 5 个或更多染色体臂改变的患者中,有 23%的患者发生致命性癌症的几率高出 5.3 倍(95%置信区间,2.2 至 13.1),而这些患者的 Gleason 评分相同且没有预测到非整倍体。即使在高风险 Gleason 评分 8-10 肿瘤的男性中,非整倍体也与死亡率相关。这些结果表明非整倍体在原发性前列腺癌中驱动侵袭性疾病方面起着关键作用。

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