Volume 17, Issue 3 (May 2015) 17, 373–380; doi: 10.4103/1008-682X.150842
Roles of the Y chromosome genes in human cancers
Tatsuo Kido, Yun-Fai Chris Lau
Division of Cell and Developmental Genetics, Department of Medicine, Veterans Affairs Medical Center, and Institute for Human Genetics, University of California, San Francisco, California 94121, USA
Correspondence: Dr. YFC Lau (Chris.Lau@UCSF.edu)
2015-3-27
Abstract |
Male and female differ genetically by their respective sex chromosome composition, i.e. XY as male and XX as female. Although both X and Y chromosomes evolved from the same ancestor pair of autosomes, the Y chromosome harbors male specific genes, which play pivotal roles in male sex determination, germ cell differentiation, and masculinization of various tissues. Deletions or translocation of the sex-determining gene, SRY, from the Y chromosome causes disorders of sex development (DSD) (previously termed as intersex condition) with dysgenic gonads. Failure of gonadal development results not only in infertility, but also in increased risks of germ cell tumor, such as gonadoblastoma and various types of testicular germ cell tumor. Recent studies demonstrate that either loss of Y chromosome or ectopic expression of Y chromosome genes are closely associated with various male-biased diseases, including selected somatic cancers. These observations suggest that the Y-linked genes are involved in male health and diseases in more frequently than expected. Although only a small number of protein-coding genes are present in the male specific region of Y chromosome, the impacts of Y chromosome genes on human diseases are still largely unknown, due to lack of in vivo models and differences between the Y chromosomes of human and rodents. In this review, we highlight the involvement of selected Y chromosome genes in cancer development in men.
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