Expression of splice variants of CD44 in thyroid neoplasms derived from follicular cells

被引:20
作者
Gu, J
Daa, T
Kashima, K
Yokoyama, S
Nakayama, I [1 ]
Noguchi, S
机构
[1] Oita Med Univ, Dept Pathol 1, Oita 87955, Japan
[2] Noguchi Thyroid Clin & Hosp Fdn, Beppu, Oita, Japan
关键词
base sequencing; CD44 splice variants; immunohistochemistry; RT-PCR; thyroid neoplasm;
D O I
10.1111/j.1440-1827.1998.tb03891.x
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Isoform expression of CD44 in follicular carcinoma (FC) of the thyroid was analyzed by immunohistochemical staining and compared to the isoforms in follicular adenoma (FA) and papillary carcinoma (PC) of the thyroid. Variant isoforms of CD44 (CD44v) were detected in these neoplastic cells but not in non-neoplastic cells. CD44v6 was expressed in PC with nodal metastasis and also in FC at significantly higher frequencies than those in PC without metastasis and FA. The frequency of expression of CD44v3 was significantly higher in PC with nodal metastasis than in PC without metastasis, The reverse transcription-polymerase chain reaction (RT-PCR) followed by Southern blotting analysis revealed the presence of a transcript for a variant of CD44 that contained variant exon 6 in FA, FC and PC. DNA sequencing of the products of RT-PCR yielded three species of cDNA for CD44v. One of the cDNA corresponded to a transcript that contained variant exon 6. These results suggest that immunohistochemical staining and RT-PCR with Southern blotting analysis for CD44v6 might be a useful diagnostic tool for the differentiation of FC from FA and that the expression of CD44v3 and CD44v6 might be important for the development of nodal metastasis in cases of PC.
引用
收藏
页码:184 / 190
页数:7
相关论文
共 23 条
[1]   PARTICIPATION IN NORMAL IMMUNE-RESPONSES OF A METASTASIS-INDUCING SPLICE VARIANT OF CD44 [J].
ARCH, R ;
WIRTH, K ;
HOFMANN, M ;
PONTA, H ;
MATZKU, S ;
HERRLICH, P ;
ZOLLER, M .
SCIENCE, 1992, 257 (5070) :682-685
[2]   CD44 IS THE PRINCIPAL CELL-SURFACE RECEPTOR FOR HYALURONATE [J].
ARUFFO, A ;
STAMENKOVIC, I ;
MELNICK, M ;
UNDERHILL, CB ;
SEED, B .
CELL, 1990, 61 (07) :1303-1313
[3]  
BROOKS L, 1995, AM J PATHOL, V146, P1102
[4]   CELL-ADHESION AND THE MOLECULAR PROCESSES OF MORPHOGENESIS [J].
EDELMAN, GM .
ANNUAL REVIEW OF BIOCHEMISTRY, 1985, 54 :135-169
[5]  
Ermak G, 1996, CANCER RES, V56, P1037
[6]  
ERMAK G, 1995, CANCER RES, V55, P4594
[7]   PREFERENTIAL EXPRESSION OF THE CELL-ADHESION MOLECULE CD44 IN PAPILLARY THYROID-CARCINOMA [J].
FIGGE, J ;
DELROSARIO, AD ;
GERASIMOV, G ;
DEDOV, I ;
BRONSTEIN, M ;
TROSHINA, K ;
ALEXANDROVA, G ;
KALLAKURY, BVS ;
BUI, HX ;
BRATSLAVSKY, G ;
ROSS, JS .
EXPERIMENTAL AND MOLECULAR PATHOLOGY, 1994, 61 (03) :203-211
[8]   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
[9]  
HEDLINGER C, 1988, WHO INT HIST CLASSIF, P3
[10]   LYMPHOCYTE RECOGNITION OF HIGH ENDOTHELIUM - ANTIBODIES TO DISTINCT EPITOPES OF AN 85-95-KD GLYCOPROTEIN ANTIGEN DIFFERENTIALLY INHIBIT LYMPHOCYTE BINDING TO LYMPH-NODE, MUCOSAL, OR SYNOVIAL ENDOTHELIAL-CELLS [J].
JALKANEN, S ;
BARGATZE, RF ;
DELOSTOYOS, J ;
BUTCHER, EC .
JOURNAL OF CELL BIOLOGY, 1987, 105 (02) :983-990