Title | Aneuploidy drives lethal progression in prostate cancer. |
Publication Type | Journal Article |
Year of Publication | 2019 |
Authors | Stopsack KH, Whittaker CA, Gerke TA, Loda M, Kantoff PW, Mucci LA, Amon A |
Journal | Proc Natl Acad Sci U S A |
Volume | 116 |
Issue | 23 |
Pagination | 11390-11395 |
Date Published | 2019 06 04 |
ISSN | 1091-6490 |
Keywords | Adult, Aged, Aneuploidy, Chromosome Aberrations, Disease Progression, Gene Expression Profiling, Humans, Male, Middle Aged, Neoplasm Grading, Neoplasm Staging, Prostate, Prostatic Neoplasms, Transcriptome |
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. |
DOI | 10.1073/pnas.1902645116 |
Alternate Journal | Proc Natl Acad Sci U S A |
PubMed ID | 31085648 |
PubMed Central ID | PMC6561291 |
Grant List | P50 CA090381 / CA / NCI NIH HHS / United States P30 CA014051 / CA / NCI NIH HHS / United States P30 CA008748 / CA / NCI NIH HHS / United States P01 CA228696 / CA / NCI NIH HHS / United States R01 CA136578 / CA / NCI NIH HHS / United States P30 CA006516 / CA / NCI NIH HHS / United States R01 CA206157 / CA / NCI NIH HHS / United States R35 GM118066 / GM / NIGMS NIH HHS / United States / HHMI / Howard Hughes Medical Institute / United States U01 CA167552 / CA / NCI NIH HHS / United States |
Related Faculty:
Massimo Loda, M.D.