Testicular cells showing characteristics of seminoma, or testicular cancerWIKIMEDIA, NEPHRONEvolution may have favored a particular genetic change as humans migrated out of Africa that led to the prevalence of testicular cancer in white men compared to black men, according to researchers in the U.K. Gareth Bond, a molecular biologist at the Ludwig Institute for Cancer Research in Oxford, and colleagues found that a single nucleotide polymorphism (SNP) in a protein acted upon by the p53 gene, mutations in which cause a variety of cancers, can lead to increased melanocyte production when UV light damages cells, thereby protecting skin from further sun damage. But the same mutation also leads to the uncontrolled proliferation of other cells in the body. They reported their findings in Cell on Thursday (October 10).
The suspect protein, called KIT ligand (KITLG), is mutated in 80 percent of Caucasian Europeans but only 24 percent of people of African descent. Testicular cancer is 4–5 times more prevalent in white men than black men, and skin cancers are far more common in people with fairer skin as well. Previous research had identified SNPs in KITLG as major contributors to testicular cancer, and Bond and his colleagues found one such SNP in KITLG that interacted with p53 to regulate cell division.
When the team exposed p53 knockout mice to UV radiation, the rodents could not produce any KITLG. But in wild-type mice, KITLG production doubled upon UV exposure, triggering melanocyte production. This could mean that the deleterious SNP in KITLG was allowed to ...
