Reed-Sternberg cell genome expression supports a B-cell lineage

J Cossman, CM Annunziata, S Barash… - Blood, The Journal …, 1999 - ashpublications.org
J Cossman, CM Annunziata, S Barash, L Staudt, P Dillon, WW He, P Ricciardi-Castagnoli
Blood, The Journal of the American Society of Hematology, 1999ashpublications.org
Abstract The malignant Reed-Sternberg cell of Hodgkin's disease, first described a century
ago, has resisted in-depth analysis due to its extreme rarity in lymphomatous tissue. To
directly study its genome-wide gene expression, approximately 11,000,000 bases (27,518
cDNA sequences) of expressed gene sequence was determined from living single Reed-
Sternberg cells, Hodgkin's tissue, and cell lines. This approach increased the number of
genes known to be expressed in Hodgkin's disease by 20-fold to 2,666 named genes. The …
Abstract
The malignant Reed-Sternberg cell of Hodgkin’s disease, first described a century ago, has resisted in-depth analysis due to its extreme rarity in lymphomatous tissue. To directly study its genome-wide gene expression, approximately 11,000,000 bases (27,518 cDNA sequences) of expressed gene sequence was determined from living single Reed-Sternberg cells, Hodgkin’s tissue, and cell lines. This approach increased the number of genes known to be expressed in Hodgkin’s disease by 20-fold to 2,666 named genes. The data here indicate that Reed-Sternberg cells from both nodular sclerosing and lymphocyte predominant Hodgkin’s disease were derived from an unusual B-cell lineage based on a comparison of their gene expression to approximately 40,000,000 bases (105 sequences) of expressed gene sequence from germinal center B cells (GCB) and dendritic cells. The data set of expressed genes, reported here and on the World Wide Web, forms a basis to understand the genes responsible for Hodgkin’s disease and develop novel diagnostic markers and therapies. This study of the rare Reed-Sternberg cell, concealed in its heterogenous cellular context, also provides a formidable test case to advance the limit of analysis of differential gene expression to the single disease cell.
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