» Articles » PMID: 17534929

Hypomethylation of PRAME is Responsible for Its Aberrant Overexpression in Human Malignancies

Overview
Date 2007 May 31
PMID 17534929
Citations 35
Authors
Affiliations
Soon will be listed here.
Abstract

The preferentially expressed antigen of melanoma (PRAME) is expressed at high levels in large fractions of human malignancies, e.g., acute myeloid leukemia. Therefore, PRAME is an important marker for diagnosis of various malignant diseases and a relevant parameter for monitoring minimal residual disease. It is supposed to be involved in tumorigenic processes. Because of these important aspects we investigated its transcriptional regulation in detail. Most relevant was a detailed DNA methylation analysis of the PRAME 5' region by genomic sequencing in correlation with PRAME expression in various human patient samples and cell lines. In combination with DNA-truncation/transfection experiments with respect to DNA methylation, we show that changes in the methylation pattern in defined parts of the regulatory regions of PRAME are sufficient for its upregulation in cells usually not expressing the gene.

Citing Articles

EZH2 inhibition sensitizes retinoic acid-driven senescence in synovial sarcoma.

Mushtaq M, Liano-Pons J, Wang J, Alzrigat M, Yuan Y, Ruiz-Perez M Cell Death Dis. 2024; 15(11):836.

PMID: 39550391 PMC: 11569238. DOI: 10.1038/s41419-024-07176-6.


The Utilization of PRAME in the Diagnosis, Prognosis, and Treatment of Melanoma.

Blount S, Liu X, McBride J Cells. 2024; 13(20.

PMID: 39451258 PMC: 11505691. DOI: 10.3390/cells13201740.


PRAME expression in melanoma is negatively regulated by TET2-mediated DNA hydroxymethylation.

Fang R, Vallius T, Zhang A, Van Cura D, Alicandri F, Fischer G bioRxiv. 2024; .

PMID: 39091741 PMC: 11291125. DOI: 10.1101/2024.07.26.605293.


Targeting PRAME for acute myeloid leukemia therapy.

Yang J, Chen M, Ye J, Ma H Front Immunol. 2024; 15:1378277.

PMID: 38596687 PMC: 11002138. DOI: 10.3389/fimmu.2024.1378277.


Expression of Immunotherapy Target PRAME in Cancer Correlates with Histone H3 Acetylation and Is Unrelated to Expression of Methylating (DMNT3A/3B) and Demethylating (TET1) Enzymes.

Kaczorowski M, Lasota J, Dudek K, Malkiewicz B, Miettinen M, Halon A J Clin Med. 2024; 13(6).

PMID: 38541782 PMC: 10971184. DOI: 10.3390/jcm13061554.