EXPRESSION OF THE INSULIN-LIKE GROWTH FACTOR-BINDING PROTEIN-3 (IGFBP-3) GENE IS INCREASED IN HUMAN RENAL CARCINOMAS

被引:32
作者
HINTZ, RL
BOCK, S
THORSSON, AV
BOVENS, J
POWELL, DR
JAKSE, G
PETRIDES, PE
机构
[1] ST JOSEPHS HOSP,DEPT PEDIAT,REYKJAVIK,ICELAND
[2] BAYLOR UNIV,DEPT PEDIAT,HOUSTON,TX
[3] GESELL STRAHLEN & UMWELTFORSCH MBH,INST CLIN HEMATOL,MUNICH,GERMANY
[4] STANFORD UNIV,DEPT PEDIAT,STANFORD,CA 94305
[5] UNIV MUNICH,KLINIKUM GROSSHADERN,DEPT MED 3,MOLEC ONCOL LAB,W-8000 MUNICH 70,GERMANY
[6] RHEIN WESTFAL TH AACHEN,SCH MED,DEPT UROL,W-5100 AACHEN,GERMANY
关键词
CARCINOMA; RENAL CELL; PEPTIDES; GROWTH SUBSTANCES;
D O I
10.1016/S0022-5347(17)38031-X
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
After we had established that the IGFBP-3 gene is expressed in normal human kidney we examined renal adenocarcinoma tissue for alterations of the expression of this gene. For this purpose we prepared poly(A)+ RNA from normal kidney tissue and adjacent renal adenocarcinoma of 18 adult patients and compared the levels of IGFBP-3 mRNA by Northern analysis in both samples. The mean content by densitometry was markedly increased in the carcinoma tissues; in 17 of 18 patients the carcinoma contained significantly more IGFBP-3 mRNA than the normal kidney sample. The highest mRNA levels were found in patients with N2 and N3 lymph node extensions. Comparative Southern analysis of paired samples of four of these patients did not reveal amplification of the gene as the cause of these increased mRNA levels. In one patient, however, we identified a restriction fragment length polymorphism (RFLP) present in normal and malignant cellular DNA. This suggests a participation of the IGFBP-3 gene in the development of human renal cell cancer.
引用
收藏
页码:1160 / 1163
页数:4
相关论文
共 24 条
[1]  
AMBS KE, 1989, UROL RES, V17, P251
[2]   IGF-I IMMUNOREACTIVITY IS EXPRESSED BY REGENERATING RENAL TUBULAR CELLS AFTER ISCHEMIC-INJURY IN THE RAT [J].
ANDERSSON, G ;
JENNISCHE, E .
ACTA PHYSIOLOGICA SCANDINAVICA, 1988, 132 (04) :453-457
[3]   SYNTHESIS AND BINDING OF INSULIN-LIKE GROWTH FACTOR-I BY HUMAN GLOMERULAR MESANGIAL CELLS [J].
ARON, DC ;
ROSENZWEIG, JL ;
ABBOUD, HE .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1989, 68 (03) :585-591
[4]   A KEY FUNCTIONAL-ROLE FOR THE INSULIN-LIKE GROWTH FACTOR-I N-TERMINAL PENTAPEPTIDE [J].
BAGLEY, CJ ;
MAY, BL ;
SZABO, L ;
MCNAMARA, PJ ;
ROSS, M ;
FRANCIS, GL ;
BALLARD, FJ ;
WALLACE, JC .
BIOCHEMICAL JOURNAL, 1989, 259 (03) :665-671
[5]   DEMONSTRATION OF INSULIN-LIKE GROWTH-FACTOR (IGF-I AND IGF-II) RECEPTORS AND BINDING-PROTEIN IN HUMAN-BREAST CANCER CELL-LINES [J].
DELEON, DD ;
BAKKER, B ;
WILSON, DM ;
HINTZ, RL ;
ROSENFELD, RG .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 152 (01) :398-405
[7]  
DROP SLS, 1989, INSULIN LIKE GROWTH
[8]   COMPENSATORY RENAL GROWTH - ROLE OF GROWTH-HORMONE AND INSULIN-LIKE GROWTH FACTOR-I [J].
ELNAHAS, AM ;
LECARPENTIER, JE ;
BASSETT, AH .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 1990, 5 (02) :123-129
[9]   IDENTIFICATION OF A CHROMOSOME-18Q GENE THAT IS ALTERED IN COLORECTAL CANCERS [J].
FEARON, ER ;
CHO, KR ;
NIGRO, JM ;
KERN, SE ;
SIMONS, JW ;
RUPPERT, JM ;
HAMILTON, SR ;
PREISINGER, AC ;
THOMAS, G ;
KINZLER, KW ;
VOGELSTEIN, B .
SCIENCE, 1990, 247 (4938) :49-56
[10]  
FREEMAN MR, 1989, CANCER RES, V49, P6221