Transforming growth factor beta 1 is significantly elevated in plasma of patients suffering from renal cell carcinoma

被引:66
作者
Junker, U
Knoefel, B
Nuske, K
Rebstock, K
Steiner, T
Wunderlich, H
Junker, K
Reinhold, D
机构
[1] THUERINGEN KRANKENHAUS SAALFELD,AGRIOCLAKRANKENHAUS,SAALFELD,GERMANY
[2] UNIV JENA,UROL CLIN,D-6900 JENA,GERMANY
[3] UNIV JENA,INST HUMAN GENET & ANTHROPOL,D-6900 JENA,GERMANY
[4] UNIV MAGDEBURG,INST EXPT INTERNAL MED,CTR INTERNAL MED,D-39106 MAGDEBURG,GERMANY
关键词
TGF-beta; 1; renal cell carcinoma; plasma level; immunomodulation;
D O I
10.1006/cyto.1996.0105
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
The levels of active and latent transforming growth factor beta 1 (aTGF-beta 1, ITGF-beta 1, respectively) in plasma samples were measured by enzyme-linked immunoabsorbent assay (ELISA). Samples were collected from patients suffering from renal cell carcinoma (RCC) before they underwent tumour resection, In all cases tested, the levels of latent TGF-beta 1 were much higher (n = 23, 41.0 +/- 13.9, range 19.3-78.1 ng/ml) than in healthy controls (n = 21, 3.8 +/- 2.9, range 0.6-9.9, P much less than 0.0001), while active TGF-beta 1 did not differ that impressively (n = 38, 1.2 +/- 1.3, range 0.0-4.5 for RCC, n = 21, 0.1 +/- 0.2, range 0.0-1.1 in controls, P < 0.001), As for TGF-beta 1 production by proximal tubulus cells has been shown, it was speculated that these high TGF-beta 1 levels might be due to secretion by the tumour, which usually originates from proximal tubuli. Indeed, production of TGF-beta 1 was found in culture supernatants, and it was possible to show TGF-beta 1 mRNA expression in tumour samples, This TGF-beta 1 was predominantly secreted in the latent form, This is in contrast to data from other authors, who found TGF-beta 1 to be secreted mainly in the active form, but need not mean that it is inactive locally as the low pH encountered within tumours is in the range necessary for its activation, It is concluded that elevated latent TGF-beta 1 is common in RCC, is at least partially produced by the tumour and might be a cause for local immunosuppressive effects within the tumour. (C) 1996 Academic Press Limited
引用
收藏
页码:794 / 798
页数:5
相关论文
共 18 条
[1]   THE CELL BIOLOGY OF TRANSFORMING GROWTH-FACTOR-BETA [J].
BARNARD, JA ;
LYONS, RM ;
MOSES, HL .
BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1032 (01) :79-87
[2]  
CERWENKA A, 1994, J IMMUNOL, V153, P4367
[3]   IMPROVED SANDWICH ENZYME-LINKED IMMUNOSORBENT ASSAYS FOR TRANSFORMING GROWTH FACTOR-BETA-1 [J].
DANIELPOUR, D .
JOURNAL OF IMMUNOLOGICAL METHODS, 1993, 158 (01) :17-25
[4]   ACTIVE AND ACID-ACTIVATABLE TGF-BETA IN HUMAN SERA, PLATELETS AND PLASMA [J].
GRAINGER, DJ ;
MOSEDALE, DE ;
METCALFE, JC ;
WEISSBERG, PL ;
KEMP, PR .
CLINICA CHIMICA ACTA, 1995, 235 (01) :11-31
[5]   TREATMENT OF ADVANCED RENAL-CELL CARCINOMA USING REGIONAL ARTERIAL ADMINISTRATION OF LYMPHOKINE-ACTIVATED KILLER-CELLS IN COMBINATION WITH LOW-DOSES OF RIL-2 [J].
HAYAKAWA, M ;
HATANO, T ;
OGAWA, Y ;
GAKIYA, M ;
OGURA, H ;
OSAWA, A .
UROLOGIA INTERNATIONALIS, 1994, 53 (03) :117-124
[6]  
HILLMAN GG, 1994, CLIN EXP IMMUNOL, V6, P476
[7]  
Knoefel B., 1995, Immunitaet und Infektion, V23, P72
[8]  
Larsson P, 1994, Scand J Urol Nephrol Suppl, V165, P1
[9]   INTERLEUKIN-6 (IL-6) FUNCTIONS AS AN INVITRO AUTOCRINE GROWTH-FACTOR IN RENAL-CELL CARCINOMAS [J].
MIKI, S ;
IWANO, M ;
MIKI, Y ;
YAMAMOTO, M ;
TANG, B ;
YOKOKAWA, K ;
SONODA, T ;
HIRANO, T ;
KISHIMOTO, T .
FEBS LETTERS, 1989, 250 (02) :607-610
[10]   EXPRESSION OF HIGH-AFFINITY INTERLEUKIN-4 RECEPTORS ON HUMAN RENAL-CELL CARCINOMA-CELLS AND INHIBITION OF TUMOR-CELL GROWTH-INVITRO BY INTERLEUKIN-4 [J].
OBIRI, NI ;
HILLMAN, GG ;
HAAS, GP ;
SUD, S ;
PURI, RK .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (01) :88-93