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Clinical Cancer Research Vol. 10, 2928-2935, May 1, 2004
© 2004 American Association for Cancer Research


Molecular Oncology, Markers, Clinical Correlates

DNA Methylation Profiles of Lymphoid and Hematopoietic Malignancies

Takao Takahashi1, Narayan Shivapurkar1,2, Jyotsna Reddy1, Hisayuki Shigematsu1, Kuniharu Miyajima1, Makoto Suzuki1, Shinichi Toyooka1, Sabine Zöchbauer-Müller3, Johannes Drach3, Gunjan Parikh1, Yingye Zheng4, Ziding Feng4, Steven H. Kroft2, Charles Timmons2, Robert W. McKenna2 and Adi F. Gazdar1,2

1 Hamon Center for Therapeutic Oncology Research and 2 Department of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas; 3 Clinical Division of Oncology, Department of Medicine I, University Hospital, Vienna, Austria; and 4 Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington

ABSTRACT

Purpose: Aberrant methylation of the 5' gene promoter regions is an epigenetic phenomenon that is the major mechanism for silencing of tumor suppressor genes in many cancer types. The aims of our study were (a) to compare the methylation profiles of the major forms of hematological malignancies and (b) to determine the methylation profile of monoclonal gammopathy of undetermined significance (MGUS) and compare it with that of multiple myeloma (MM).

Experimental Design: We compared the aberrant promoter methylation profile of 14 known or suspected tumor suppressor genes in leukemias (n = 48), lymphomas (n = 42), and MMs (n = 40). We also examined the methylation profile of MGUS (n = 20), a premalignant plasma cell dyscrasia. The genes studied represent five of the six "hallmarks of cancer."

Results: Peripheral blood lymphocytes (n = 14) from healthy volunteers were negative for methylation of all genes, and methylation percentages in 41 nonmalignant tissues (peripheral blood mononuclear cells, bone marrows, and lymph nodes) from hematological patients were low (0–9%) for all 14 genes, confirming that methylation was tumor specific. Ten of the genes were methylated at frequencies of 29–68% in one or more tumor types, and the methylation indices (an indicator of overall methylation) varied from 0.25 to 0.34. With two exceptions, the methylation patterns of leukemias and lymphomas were similar. However, the pattern of MMs varied from the other tumor types for six genes. In general, the methylation pattern of MGUS was similar to that of MM, although the methylation frequencies were lower (the methylation index of MGUS was 0.15, and that of MM was 0.3). However, the methylation frequencies of six genes were significantly higher in MGUS than in control tissues. The relatively high frequencies of methylation in MGUS are consistent with it being a premalignant condition.

Conclusions: The three major forms of lymphoid/hematopoietic malignancies show overlapping but individual patterns of methylation.




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Copyright © 2004 by the American Association for Cancer Research.