Biologic characteristics of patients with hypocellular myelodysplastic syndromes

被引:18
作者
Goyal, R
Qawi, H
Ali, I
Dar, S
Mundle, S
Shetty, V
Mativi, Y
Allampallam, K
Lisak, L
Loew, J
Venugopal, P
Gezer, S
Robin, E
Rifkin, S
Raza, A
机构
[1] Rush Presbyterian St Lukes Med Ctr, Rush Canc Inst, Chicago, IL 60612 USA
[2] Rush Presbyterian St Lukes Med Ctr, Dept Pathol, Chicago, IL 60612 USA
[3] Ingalls Mem Hosp, Harvey, IL USA
[4] NW Community Hosp, Arlington Hts, IL USA
关键词
hypocellular myelodysplastic syndromes; apoptosis; proliferation; TNF-alpha; TGF-beta; chromosomes; 5; and/or; 7;
D O I
10.1016/S0145-2126(98)00187-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Rates of proliferation and apoptosis as well as expression of tumor necrosis factor alpha (TNF-alpha), transforming growth factor beta (TGF-beta) and the number of macrophages were measured in bone marrow (BM) biopsies of 33 patients who presented with hypocellular (cellularity < 30%) myelodysplastic syndromes (MDS). Results showed that 2/3 of the patients had high apoptosis, high cytokine levels and large number of macrophages in their biopsies while 1/3 did not. Apoptosis and TNF-alpha levels were directly related (r = 0.583, P = 0.003, n = 24) as was apoptosis and the degree of anemia (P = 0.033, n = 18). A subgroup of patients with abnormalities of chromosomes 5 or 7 had higher platelets (P = 0.026) and higher apoptosis (P = 0.038) when compared with the rest of the group. Eight patients had no evidence of apoptosis and almost no detectable TNF-alpha in their biopsies. We conclude that within the hypocellular variant of MDS, then may be two distinct sub-groups of patients, one who present with high cytokine-mediated intramedullary apoptosis and the other who may be better characterized as having a stem-cell failure defect since they showed no evidence of apoptosis. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:357 / 364
页数:8
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