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Selective loss of B-cell phenotype in lymphocyte predominant Hodgkin lymphoma (2007)_香港中文大学

香港中文大学 辅仁网/2017-06-27

Selective loss of B-cell phenotype in lymphocyte predominant Hodgkin lymphoma
Publication in refereed journal


香港中文大学研究人员 ( 现职)
陶谦教授 (肿瘤学系)


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Web of Sciencehttp://aims.cuhk.edu.hk/converis/portal/Publication/11WOS source URL

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摘要The neoplastic Reed-Sternberg cells characteristic of classical Hodgkin's lymphoma (cHL) are of B-cell origin but they almost always show striking loss of a range of B-cell-associated molecules. In contrast, the neoplastic cells found in lymphocyte predominant Hodgkin's lymphoma (LPHL) (L&H cells) are traditionally thought of as possessing the full repertoire of features associated with germinal centre B cells (eg BCL-6 expression, 'ongoing' Ig gene mutation). In the present paper, we report an extensive phenotypic analysis of L&H cells which revealed down-regulation of a number of markers associated with the B-cell lineage (eg CD19, CD37) and with the germinal centre maturation stage (eg PAG, LCK). The promoter methylation status of three of these down-regulated genes (CD10, CD19, and LCK) was further studied in microdissected L&H cells, and this revealed that their promoters were unmethylated. In contrast, these genes showed promoter methylation in cell lines derived from CHL. Further investigation of the mechanisms responsible for the deregulation of these molecules in L&H cells may provide new insights into the genetic abnormalities underlying LPHL. Copyright (c) 2007 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

着者Tedoldi S, Mottok A, Ying J, Paterson JC, Cui Y, Facchetti F, van Krieken JHJM, Ponzoni M, Ozkal S, Masir N, Natkunam Y, Pileri SA, Hansmann ML, Mason DY, Tao Q, Marafioti T
期刊名称Journal of Pathology
出版年份2007
月份12
日期1
卷号213
期次4
出版社JOHN WILEY & SONS LTD
页次429 - 440
国际标準期刊号0022-3417
电子国际标準期刊号1096-9896
语言英式英语

关键词immunohistochemistry; lPHL; methylation; microdissection
Web of Science 学科类别Oncology; ONCOLOGY; Pathology; PATHOLOGY

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