Promoter DNA methylation of CD10 in lymphoid malignancies.
Promoter DNA methylation of CD10 in lymphoid malignancies.
复制标题
淋巴恶性肿瘤中 CD10 的启动子 DNA 甲基化。
DOI:
10.1038/sj.leu.2404353
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发表时间:
2006
期刊:
影响因子:
11.4
通讯作者:
Caldwell,CW
中科院分区:
文献类型:
--
作者:
Taylor,KH;Liu,J;Guo,J;Davis,JW;Shi,H;Caldwell,CW
Lymphopoiesis of B-lineage cells is a complex process requiring stage-specific expression of multiple surface and cytoplasmic proteins that contribute to development and function. This complex process comprises biological progression from a lymphoid progenitor cell to a terminally differentiated plasma cell. Each step in this normal biological progression also has a malignant counterpart either referred to as leukemia or lymphoma (Figure 1a and b). 1 The neutral endopeptidase 24.11,(NEP or CD10), is considered a regulator of B-cell growth and proliferation. 2 The enzyme is a cell surface aminopeptidase capable of degrading a number of bioactive peptides with various functions that depend on the cell type or tissue of origin and is active in early bone marrow (BM) precursor B cells and lymph node germinal center (GC) B cells. In addition, CD10 is expressed in malignancies including precursor B cell acute lymphocytic leukemia (B-ALL), GC-related non-Hodgkin’s lymphoma (NHL) such as Burkitt’s lymphoma and follicular lymphoma (FL), and GC-related diffuse large B-cell lymphomas (DLBCL). It is not, however, expressed in terminally differentiated plasma cells of multiple myeloma (MM), in the pre-GC cells of mantle cell lymphoma (MCL), or in the pre-or post-GC cells of B-cell chronic lymphocytic leukemia (B-CLL). Thus, there is a biphasic pattern of CD10 cell surface protein expression that correlates with specific stages of development in both normal and neoplastic B cells and precursor B cells (Figure 1c).