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MGMT and CALCA promoter methylation are associated with poor prognosis in testicular germ cell tumor patients.


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 (VGF, MGMT, ADAMTS1, CALCA, HOXA9, CDKN2B, CDO1 and NANOG) was evaluated in 72 primary TGCT by quantitative methylation specific PCR. A high frequency of MGMT (90.9%, 20/22; p=0.019) and CALCA (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 MGMT and 51.3% vs 77.0%; p=0.029 for CALCA). The findings of this study indicate that methylation of MGMT and CALCA are frequent and could be used as new molecular markers of prognosis in TGCT.

SUBMITTER: Martinelli CMDS 

PROVIDER: S-EPMC5584175 | biostudies-literature | 2017 Aug

REPOSITORIES: biostudies-literature

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MGMT and CALCA promoter methylation are associated with poor prognosis in testicular germ cell tumor patients.

Martinelli Camila Maria da Silva CMDS   Lengert André van Helvoort AVH   Cárcano Flavio Mavignier FM   Silva Eduardo Caetano Albino ECA   Brait Mariana M   Lopes Luiz Fernando LF   Vidal Daniel Onofre DO  

Oncotarget 20160810 31


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 (<i>VGF, MGMT, ADAMTS1</i>, <i>CALCA</i>,  ...[more]

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