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Priority Reports |
1 Genetics Branch and 2 Laboratory of Pathology, NIH/National Cancer Institute; 3 Pathology Department, Suburban Hospital, Bethesda, Maryland; 4 Illumina, Inc., San Diego, California; and 5 School of Medicine, University of California-San Francisco, San Francisco, California
Requests for reprints: Paul S. Meltzer, Room 6138, 37 Convent Drive, MSC 4265, Bethesda, MD 20892-4265. Phone: 301-496-5266; Fax: 301-480-3281; E-mail: pmeltzer{at}mail.nih.gov.
Key Words: follicular lymphoma methylation profiling epigenetics FFPE pathology
Emerging technologies allow broad profiling of the cancer genome for differential DNA methylation relative to benign cells. Herein, bisulfite-modified DNA from lymph nodes with either reactive hyperplasia or follicular lymphoma (FL) were analyzed using a commercial C/UpG genotyping assay. Two hundred fifty-nine differentially methylated targets (DMT) distributed among 183 unique genes were identified in FL. Comparison of matched formalin-fixed, paraffin-embedded and frozen surgical pathology replicates showed the complete preservation of the cancer methylome among differently archived tissue specimens. Analysis of the DMT profile is consistent with a pervasive epigenomic remodeling process in FL that affects predominantly nonlymphoid genes. [Cancer Res 2009;69(3):758–64]
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