Loss of chromosome Y in primary tumors

被引:26
|
作者
Qi, Meifang [1 ,2 ,3 ]
Pang, Jiali [1 ,4 ,7 ]
Mitsiades, Irene [1 ,2 ,8 ]
Lane, Andrew A. [2 ,3 ,5 ]
Rheinbay, Esther [1 ,2 ,3 ,6 ]
机构
[1] Massachusetts Gen Hosp, Ctr Canc Res, Charlestown, MA 02129 USA
[2] Harvard Med Sch, Boston, MA 02115 USA
[3] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
[4] Harvard TH Chan Sch Publ Hlth, Boston, MA 02115 USA
[5] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02215 USA
[6] Massachusetts Gen Hosp, Dept Pathol, Boston, MA 02114 USA
[7] Shanghai Artificial Intelligence Lab, Shanghai, Peoples R China
[8] Boston Univ, Coll Arts & Sci, Boston, MA 02215 USA
关键词
CANCER DRIVER GENES; MOSAIC LOSS; MELANOMA; BLOOD; RESISTANCE; CARCINOMA; MUTATION; CELLS; RISK;
D O I
10.1016/j.cell.2023.06.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Certain cancer types afflict female and male patients disproportionately. The reasons include differences in male/female physiology, effect of sex hormones, risk behavior, environmental exposures, and genetics of the sex chromosomes X and Y. Loss of Y (LOY) is common in peripheral blood cells in aging men, and this phenomenon is associated with several diseases. However, the frequency and role of LOY in tumors is little understood. Here, we present a comprehensive catalog of LOY in >5,000 primary tumors from male patients in the TCGA. We show that LOY rates vary by tumor type and provide evidence for LOY being either a passenger or driver event depending on context. LOY in uveal melanoma specifically is associated with age and survival and is an independent predictor of poor outcome. LOY creates common dependencies on DDX3X and EIF1AX in male cell lines, suggesting that LOY generates unique vulnerabilities that could be therapeutically exploited.
引用
收藏
页码:3125 / +
页数:24
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