Ligation of the CD44 adhesion molecule inhibits drug-induced apoptosis in human myeloid leukemia cells

被引:54
作者
Allouche, M
Charrad, RS
Bettaieb, A
Greenland, C
Grignon, C
Smadja-Joffe, F
机构
[1] CHU Purpan, CNRS, UPCM, UPR2163, F-31059 Toulouse 03, France
[2] Hop Paul Brousse, INSERM, U268, Villejuif, France
[3] Ctr Claudius Regaud, INSERM, CJF 9503, Toulouse, France
[4] Fac Med & Pharm Dijon, INSERM, U517, Dijon, France
关键词
D O I
10.1182/blood.V96.3.1187.015k01_1187_1190
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Adhesion molecules can improve hematopoietic cell survival; however, their role in leukemic cell resistance to drug induced apoptosis is poorly documented. The CD44 adhesion molecule is strongly expressed on acute myeloid leukemia (AML) blasts. Using 2 myeloid cell lines, HL60 and NB4, evidence is presented that prior Incubation with the CD44-specific mono clonal antibody (mAb) A3D8, reported to induce differentiation of AML blasts, significantly decreases apoptosis induced by 3 drugs used in AML chemotherapy: daunorubicin (DNR), mitoxantrone, and etoposide, In addition, in HL60 cells, CD44 ligation with A3D8 mAb fully abrogates the DNR-triggered generation of ceramide, a lipid second messenger involved in the DNR apoptotic signaling pathway. Moreover, results show that the A3D8 mAb and Bcl-2 additively inhibit DNR-induced apoptosis in HL60 cells overexpressing Bcl-2, These results suggest that, to eradicate AML blasts, the differentiation-inducing anti-CD44 mAb A3D8 should not be administered prior to apoptosis-inducing drugs. (C) 2000 by The American Society of Hematology.
引用
收藏
页码:1187 / 1190
页数:4
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