AI Article Synopsis

  • Testicular germ cell tumors (TGCT) are a leading cause of cancer-related death in young men, with treatment-resistant cases having a poor prognosis.
  • The study found high rates of methylation in specific genes associated with non-seminomatous tumors and refractory disease, indicating potential new markers for prognosis.
  • Methylation of these genes correlates with lower survival rates, suggesting they could help predict clinical outcomes for TGCT patients.

Article Abstract

Testicular germ cell tumors (TGCT) represent the second main cause of cancer-related death in young men. Despite high cure rates, refractory disease results in poor prognosis. Epigenetic reprogramming occurs during the development of seminomas and non-seminomas. Understanding the molecular and genetic basis of these tumors would represent an important advance in the search for new TGCT molecular markers. Hence the frequency of methylation of a gene panel (, , and ) was evaluated in 72 primary TGCT by quantitative methylation specific PCR. A high frequency of (90.9%, 20/22; p=0.019) and (90.5%, 19/21; p<0.026) methylation was associated with non-seminomatous tumors while CALCA methylation was also associated with refractory disease (47.4%, 09/19; p=0.005). Moreover, promoter methylation of both genes predicts poor clinical outcome for TGCT patients (5-year EFS: 50.5% vs 77.1%; p=0.032 for and 51.3% vs 77.0%; p=0.029 for ). The findings of this study indicate that methylation of and are frequent and could be used as new molecular markers of prognosis in TGCT.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584175PMC
http://dx.doi.org/10.18632/oncotarget.11167DOI Listing

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