The methylation pattern of the human HLA-DR alpha gene was analyzed in primary tumors and lymph node metastases isolated from patients with a variety of tumors, including thyroid, pancreas, breast and gastric carcinomas and melanomas. In normal tissues (including breast, muscle, brain, sperm, T-and B-lymphocytes) the HLA-DR alpha gene is hypermethylated at CCGG and GCGC sites. In all tissues studied, the only constantly unmethylated region was located in the 5' portion of the gene. Our results indicate that the HLA-DR alpha gene is hypomethylated in metastatic lymph nodes, as well as in the carcinomas and melanomas studied. These findings lend support to the hypothesis that DNA hypomethylation of the human HLA-DR alpha gene may represent a molecular marker of malignant tumors.

Methylation state of cellular genes and oncogenes as a marker of malignancy in human carcinomas

GAMBARI, Roberto;PIVA, Maria Roberta;MISCHIATI, Carlo;DEL SENNO, Laura;NASTRUZZI, Claudio;
1989

Abstract

The methylation pattern of the human HLA-DR alpha gene was analyzed in primary tumors and lymph node metastases isolated from patients with a variety of tumors, including thyroid, pancreas, breast and gastric carcinomas and melanomas. In normal tissues (including breast, muscle, brain, sperm, T-and B-lymphocytes) the HLA-DR alpha gene is hypermethylated at CCGG and GCGC sites. In all tissues studied, the only constantly unmethylated region was located in the 5' portion of the gene. Our results indicate that the HLA-DR alpha gene is hypomethylated in metastatic lymph nodes, as well as in the carcinomas and melanomas studied. These findings lend support to the hypothesis that DNA hypomethylation of the human HLA-DR alpha gene may represent a molecular marker of malignant tumors.
1989
Barbieri, R; Gambari, Roberto; Buzzoni, D; Piva, Maria Roberta; Orlando, P; Mischiati, Carlo; DEL SENNO, Laura; Nastruzzi, Claudio; Giacomini, P; Natali, Pg
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11392/495206
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