Binding specificity of siglec7 to disialogangliosides of renal cell carcinoma: possible role of disialogangliosides in tumor progression

被引:36
作者
Ito, A
Handa, K
Withers, DA
Satoh, M
Hakomori, S
机构
[1] Pacific NW Res Inst, Seattle, WA 98122 USA
[2] Univ Washington, Dept Pathobiol, Seattle, WA 98195 USA
[3] Univ Washington, Dept Microbiol, Seattle, WA 98195 USA
[4] Tohoku Univ, Sch Med, Dept Urol, Sendai, Miyagi 980, Japan
关键词
renal cell carcinoma; metastasis; ganglioside; siglec7; adhesion; TOS-1; cell;
D O I
10.1016/S0014-5793(01)02476-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Previous studies indicate that expression of higher gangliosides in renal cell carcinoma (RCC) is correlated with metastatic potential, particularly in the lung, Out of five major gangliosides in RCC, three disialogangliosides (disialogalactosylgloboside, IV(3)NeuAcIII(6)NeuAcLc(4), and IV(4)Gal-NAclV(3)NeuAcIII(6)NeuAcLc(4)) bind strongly to siglec7, which is expressed highly in monocytes and natural killer cells. Out of other gangliosides tested, 2 -->6 sialylparagloboside, GD3, GD2, and GT1b, but not other lacto- or ganglio-series gangliosides, showed clear binding to siglec7, In view of preferential metastasis of RCC to the lung, and binding of RCC cell line TOS-1 to lung tissue sections as shown in our previous study, we examined expression of siglec7 in the lung. siglec7 is expressed highly in resident blood cells, but not in parenchymatous cells. TOS-1 cells aggregate together strongly through adhesion with peripheral blood mononuclear cells to form large clumps. This suggests the possibility that such aggregates may form embolisms of microvasculature, particularly in the lung, which initiate metastasis, Other possible roles of higher gangliosides in RCC in promoting metastasis and tumor progression are discussed. (C) 2001 Published by Elsevier Science B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:116 / 120
页数:5
相关论文
共 32 条
[11]  
ITO A, 2000, IN PRESS J BIOL CHEM
[12]   Carbohydrate-mediated cell adhesion involved in hematogenous metastasis of cancer [J].
Kannagi, R .
GLYCOCONJUGATE JOURNAL, 1997, 14 (05) :577-584
[13]  
Khatib AM, 1999, CANCER RES, V59, P1356
[14]  
KOJIMA N, 1992, J BIOL CHEM, V267, P17264
[15]   IMMUNOSUPPRESSION BY HUMAN GANGLIOSIDES .1. RELATIONSHIP OF CARBOHYDRATE STRUCTURE TO THE INHIBITION OF T-CELL RESPONSES [J].
LADISCH, S ;
BECKER, H ;
ULSH, L .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1125 (02) :180-188
[16]  
Manfredi MG, 1999, CANCER RES, V59, P5392
[17]  
McKallip R, 1999, J IMMUNOL, V163, P3718
[18]  
MIYAKE M, 1988, CANCER RES, V48, P6154
[19]   Identification and characterization of a novel siglec, siglec-7, expressed by human natural killer cells and monocytes [J].
Nicoll, G ;
Ni, J ;
Liu, D ;
Klenerman, P ;
Munday, J ;
Dubock, S ;
Mattei, MG ;
Crocker, PR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (48) :34089-34095
[20]  
Ono M, 1999, CANCER RES, V59, P2335