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://dx.doi.org/10.18632/oncotarget.11167 | DOI Listing |
Sci Rep
December 2024
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December 2024
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IRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia "Seràgnoli", Bologna, Italy.
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