CD44 expression predicts disease outcome in localized large B cell lymphoma

被引:32
作者
Drillenburg, P
Wielenga, VJM
Kramer, MHH
van Krieken, JHJM
Kluin-Nelemans, HC
Hermans, J
Heisterkamp, S
Noordijk, EM
Kluin, PM
Pals, ST
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Pathol, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Dept Clin Epidemiol & Biostat, NL-1105 AZ Amsterdam, Netherlands
[3] Leiden Univ, Med Ctr, Dept Pathol, Leiden, Netherlands
[4] Leiden Univ, Med Ctr, Dept Hematol, Leiden, Netherlands
[5] Leiden Univ, Med Ctr, Dept Med Stat, Leiden, Netherlands
[6] Univ Amsterdam, Acad Med Ctr, Dept Clin Oncol, NL-1105 AZ Amsterdam, Netherlands
[7] Ctr Comprehens Canc W, Leiden, Netherlands
关键词
CD44; cell adhesion; B cell lymphoma; prognosis;
D O I
10.1038/sj.leu.2401490
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Diffuse large B cell non-Hodgkin's lymphomas (DLCL) form a heterogeneous group of tumors with diverse morphology, clinical features, treatment response and prognosis. The biological variables underlying this heterogeneity are unknown. In the present study, we explored the value of the lymphocyte homing receptor CD44, a putative determinant of lymphoma dissemination, in predicting prognosis in DLCL. Expression of the standard form of CD44 (CD44s) and of CD44 isoforms containing exon v6 (CD44v6) on tumor cells was assessed by immunohistochemistry in a cohort of 276 DLCL patients from a population based lymphoma registry. We observed that CD44s as well as CD44v6 expression correlated with tumor dissemination in patients with primary nodal DLCL. Importantly, in patients with localized nodal disease, CD44s was a strong prognosticator predicting tumor related death independent of the other parameters of the International Prognostic Index (IPI). Incorporation of CD44s in the IPI parameter 'stage', increased the prognostic value of this parameter in nodal DLCL. Our data identify CD44 as a biological prognosticator, which can be used to 'fine-tune' the IPI for nodal DLCL.
引用
收藏
页码:1448 / 1455
页数:8
相关论文
共 50 条
[1]   CD44 IS NECESSARY FOR OPTIMAL CONTACT ALLERGIC RESPONSES BUT IS NOT REQUIRED FOR NORMAL LEUKOCYTE EXTRAVASATION [J].
CAMP, RL ;
SCHEYNIUS, A ;
JOHANSSON, C ;
PURE, E .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (02) :497-507
[2]  
CARBONE PP, 1971, CANCER RES, V31, P1860
[3]   CD44 and hyaluronan-dependent rolling interactions of lymphocytes on tonsillar stroma [J].
Clark, RA ;
Alon, R ;
Springer, TA .
JOURNAL OF CELL BIOLOGY, 1996, 134 (04) :1075-1087
[4]  
Dalla-Favera Riccardo, 1996, P139
[5]   Requirement for CD44 in activated T cell extravasation into an inflammatory site [J].
DeGrendele, HC ;
Estess, P ;
Siegelman, MH .
SCIENCE, 1997, 278 (5338) :672-675
[6]   CD44 and its ligand hyaluronate mediate rolling under physiologic flow: A novel lymphocyte-endothelial cell primary adhesion pathway [J].
DeGrendele, HC ;
Estess, P ;
Picker, LJ ;
Siegelman, MH .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (03) :1119-1130
[7]   A NEW VARIANT OF GLYCOPROTEIN CD44 CONFERS METASTATIC POTENTIAL TO RAT CARCINOMA-CELLS [J].
GUNTHERT, U ;
HOFMANN, M ;
RUDY, W ;
REBER, S ;
ZOLLER, M ;
HAUSSMANN, I ;
MATZKU, S ;
WENZEL, A ;
PONTA, H ;
HERRLICH, P .
CELL, 1991, 65 (01) :13-24
[8]  
HARRIS NL, 1994, BLOOD, V84, P1361
[9]   Splice variants of the cell surface glycoprotein CD44 associated with metastatic tumour cells are expressed in normal tissues of humans and cynomolgus monkeys [J].
Heider, KH ;
Mulder, JWR ;
Ostermann, E ;
Susani, S ;
Patzelt, E ;
Pals, ST ;
Adolf, GR .
EUROPEAN JOURNAL OF CANCER, 1995, 31A (13-14) :2385-2391
[10]   INTERNATIONAL PROGNOSTIC INDEX FOR AGGRESSIVE NON-HODGKINS-LYMPHOMA IS VALID FOR ALL MALIGNANCY GRADES [J].
HERMANS, J ;
KROL, ADG ;
VANGRONINGEN, K ;
KLUIN, PM ;
KLUINNELEMANS, JC ;
KRAMER, MHH ;
NOORDIJK, EM ;
ONG, F ;
WIJERMANS, PW .
BLOOD, 1995, 86 (04) :1460-1463