The expression of Gal beta 1,4GlcNAc alpha 2,6 sialyltransferase and alpha 2,6-linked sialoglycoconjugates in human brain tumors

被引:51
作者
Kaneko, Y
Yamamoto, H
Kersey, DS
Colley, KJ
Leestma, JE
Moskal, JR
机构
[1] CHICAGO INST NEUROSURG & NEURORES,CHICAGO,IL 60614
[2] UNIV ILLINOIS,DEPT BIOCHEM,CHICAGO,IL 60612
关键词
glioma; glycosyltransferase; meningioma; metastasis; Sambucus nigra agglutinin;
D O I
10.1007/s004010050427
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
CMP-NeuAc: Gal beta 1,4GlcNAc alpha 2,6 sialyltransferase (alpha 2,6-ST) [EC 2.4.99.1] is developmentally regulated, shows a high degree of tissue specificity, and appears to play a role in oncogenic transformation and metastasis. In the present study, we have performed the first detailed analysis of the expression of alpha 2,6-ST and alpha 2,6-linked sialoglycoconjugates in human brain tumors. We used a polyclonal, monospecific anti-rat alpha 2,6-ST antibody and the alpha 2,6-linked sialic acid-specific lectin, Sambucus nigra agglutinin (SNA) for histochemical studies, and a human alpha 2,6-ST-specific cDNA probe for Northern analysis. Meningiomas, chordomas and craniopharyngiomas frequently expressed alpha 2,6-ST and alpha 2,6-linked sialoglycoconjugates. Among the different meningioma subtypes, meningothelial meningiomas stained more strongly with both anti-alpha 2,6-ST antibody and SNA than the fibroblastic and anaplastic meningiomas. On the other hand, all tumors of glial origin and medulloblastomas were virtually devoid of either alpha 2,6-ST or alpha 2,6-linked sialoglycoconjugate expression. Moreover, very weak to negligible expression of both alpha 2,6-ST and alpha 2,6-linked sialoglycoconjugates was observed in brain metastases. In conclusion, alpha 2,6-ST and alpha 2,6-linked sialoglycoconjugate expression is associated with non-neuroectodermal epithelial-like tumors.
引用
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页码:284 / 292
页数:9
相关论文
共 30 条
[1]   THE HB-6, CDW75, AND CD76 DIFFERENTIATION ANTIGENS ARE UNIQUE CELL-SURFACE CARBOHYDRATE DETERMINANTS GENERATED BY THE BETA-GALACTOSIDE ALPHA-2,6-SIALYLTRANSFERASE [J].
BAST, BJEG ;
ZHOU, LJ ;
FREEMAN, GJ ;
COLLEY, KJ ;
ERNST, TJ ;
MUNRO, JM ;
TEDDER, TF .
JOURNAL OF CELL BIOLOGY, 1992, 116 (02) :423-435
[2]  
BRAESCHANDERSEN S, 1994, J BIOL CHEM, V269, P11783
[3]  
BRESALIER RS, 1990, CANCER RES, V50, P1299
[4]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[5]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[6]  
COLLARD JG, 1986, CANCER RES, V46, P3521
[7]  
COLLEY KJ, 1992, J BIOL CHEM, V267, P7784
[8]   THE EXPRESSION OF SOLUBLE AND CELL-BOUND ALPHA-2,6 SIALYLTRANSFERASE IN HUMAN COLONIC-CARCINOMA CACO-2 CELLS CORRELATES WITH THE DEGREE OF ENTEROCYTIC DIFFERENTIATION [J].
DALLOLIO, F ;
MALAGOLINI, N ;
SERAFINICESSI, F .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 184 (03) :1405-1410
[9]   CELL CYCLE-DEPENDENT REGULATION OF CDW75 (BETA-GALACTOSIDE ALPHA-2,6-SIALYLTRANSFERASE) ON HUMAN LYMPHOCYTES-B [J].
ERIKSTEIN, BK ;
FUNDERUD, S ;
BEISKE, K ;
AASENG, A ;
DAVIES, CD ;
BLOMHOFF, HK ;
SMELAND, EB .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1992, 22 (05) :1149-1155
[10]  
FAYOS BE, 1994, J BIOL CHEM, V269, P2151