Expression of the leukemic prognostic marker CD7 is linked to epigenetic modifications in chronic myeloid leukemia

• Published in: Molecular cancer 2010-02, Vol.9 (1), p.41-41, Article 41
• Main Authors: Rogers, Sally L, Zhao, Yun, Jiang, Xiaoyan, Eaves, Connie J, Mager, Dixie L, Rouhi, Arefeh
• Format: Article
• Language: English
• Subjects: Acetylation; Adult; Aged; Antigens, CD34 - metabolism; Antigens, CD7 - genetics; Antigens, CD7 - metabolism; Biomarkers, Tumor - metabolism; Bone marrow; Cancer; Care and treatment; Case-Control Studies; Cell Line, Tumor; Chronic myeloid leukemia; DNA methylation; DNA Methylation - genetics; Epigenesis, Genetic; Female; Gene expression; Gene Expression Regulation, Leukemic; Genes; Genetic aspects; Histones - metabolism; Humans; Leukemia; Leukemia, Myelogenous, Chronic, BCR-ABL Positive - diagnosis; Leukemia, Myelogenous, Chronic, BCR-ABL Positive - enzymology; Leukemia, Myelogenous, Chronic, BCR-ABL Positive - genetics; Leukemia, Myelogenous, Chronic, BCR-ABL Positive - pathology; Male; Medical research; Methylation; Middle Aged; Physiological aspects; Prognosis; Proteins; Risk factors; RNA, Messenger - genetics; RNA, Messenger - metabolism; Serine Endopeptidases - genetics; Serine Endopeptidases - metabolism; Studies; Transcription, Genetic; Tumor markers
• ISSN: 1476-4598; 1476-4598
• DOI: 10.1186/1476-4598-9-41

Expression levels of the cell surface glycoprotein, CD7, and the serine protease, elastase 2 (ELA2), in the leukemic cells of patients with chronic myeloid leukemia (CML) have been associated with clinical outcome. However, little is known about the mechanisms that underlie the variable expression of these genes in the leukemic cells. To address this question, we compared the level of their expression with the DNA methylation and histone acetylation status of 5' sequences of both genes in leukemic cell lines and primitive (lin-CD34+) leukemic cells from chronic phase CML patients. DNA methylation of the ELA2 gene promoter did not correlate with its expression pattern in lin-CD34+ cells from chronic phase CML patient samples even though there was clear differential DNA methylation of this locus in ELA2-expressing and non-expressing cell lines. In contrast, we found a strong relation between CD7 expression and transcription-permissive chromatin modifications, both at the level of DNA methylation and histone acetylation with evidence of hypomethylation of the CD7 promoter region in the lin-CD34+ cells from CML patients with high CD7 expression. These findings indicate a link between epigenetic modifications and CD7 expression in primitive CML cells.