EPIDERMAL GROWTH-FACTOR, TRANSFORMING GROWTH-FACTOR-ALPHA, AND EPIDERMAL GROWTH-FACTOR RECEPTOR CONTENT IN NORMAL AND CARCINOMATOUS GASTRIC AND COLONIC TISSUE

被引:0
作者
BORLINGHAUS, P [1 ]
WIESER, S [1 ]
LAMERZ, R [1 ]
机构
[1] UNIV MUNICH,KLINIKUM GROSSHADERN,MED KLIN 2,MARCHIONINISTR 15,D-81366 MUNICH,GERMANY
来源
CLINICAL INVESTIGATOR | 1993年 / 71卷 / 11期
关键词
EPIDERMAL GROWTH FACTOR; TRANSFORMING GROWTH FACTOR-ALPHA; EPIDERMAL GROWTH FACTOR RECEPTOR; GROWTH FACTORS;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Epidermal growth factor (EGF) and transforming growth factor-alpha (TGF-alpha) are polypeptides which bind to the EGF receptor (EGFr) and may play a role in cell growth and carcinogenesis. Our study investigated the content of EGF, TGF-alpha, and EGFr in tumors of the stomach and the colon in comparison with the sourrounding mucosa. EGF was detected in half of the stomach specimens with concentrations between 1 and 9 ng/g weight irrespective of histology. In the colon no EGF was found in the tumor or normal mucosa. In the stomach normal mucosa contained higher TGF-alpha concentrations (mean 22.4 ng/g) than the tumors (mean 11.8 ng/g), but the difference was not statistically significant because of a wide variation in mucosal values. By contrast, the colon mucosa displayed significantly higher TGF-alpha concentrations than the tumor tissues (33 ng/g versus 12 ng/g; P < 0.01). EGFr content in the gastric mucosa was lower compared to gastric carcinoma (48 fmol/g versus 75 fmol/g) yet not significantly different. In contrast, colorectal tumor specimens disclosed significantly higher concentrations than the mucosal tissues (mean of 155 fmol/g versus 80 fmol/g; P < 0.01). In conclusion, TGF-alpha should not be considered a tumorigenic but a physiological growth factor in the stomach and colon. An elevated EGFr content in colorectal tumors in comparison with the normal mucosa could lead to a growth advantage by an autostimulating mechanism.
引用
收藏
页码:903 / 907
页数:5
相关论文
共 24 条
[1]  
ANZANO MA, 1989, CANCER RES, V49, P2898
[2]   THE OCCURRENCE OF EPIDERMAL GROWTH-FACTOR RECEPTORS AND THE CHARACTERIZATION OF EGF-LIKE FACTORS IN HUMAN OVARIAN, ENDOMETRIAL, CERVICAL AND BREAST-CANCER - EGF RECEPTORS AND FACTORS IN GYNECOLOGICAL CARCINOMAS [J].
BAUKNECHT, T ;
KOHLER, M ;
JANZ, I ;
PFLEIDERER, A .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1989, 115 (02) :193-199
[3]   LOCALIZATION OF TRANSFORMING GROWTH FACTOR-ALPHA AND ITS RECEPTOR IN GASTRIC-MUCOSAL CELLS - IMPLICATIONS FOR A REGULATORY ROLE IN ACID-SECRETION AND MUCOSAL RENEWAL [J].
BEAUCHAMP, RD ;
BARNARD, JA ;
MCCUTCHEN, CM ;
CHERNER, JA ;
COFFEY, RJ .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (03) :1017-1023
[4]  
BENNETT C, 1989, CANCER RES, V49, P2104
[5]   HUMAN EPIDERMAL GROWTH-FACTOR AND PROLIFERATION OF HUMAN FIBROBLASTS [J].
CARPENTER, G ;
COHEN, S .
JOURNAL OF CELLULAR PHYSIOLOGY, 1976, 88 (02) :227-237
[6]  
CARPENTER G, 1981, HDB EXP PHARM, V57, P89
[7]   TRANSFORMING GROWTH FACTOR-ALPHA AND EPIDERMAL GROWTH-FACTOR LEVELS IN NORMAL HUMAN GASTROINTESTINAL MUCOSA [J].
CARTLIDGE, SA ;
ELDER, JB .
BRITISH JOURNAL OF CANCER, 1989, 60 (05) :657-660
[8]   EPIDERMAL GROWTH-FACTOR RECEPTORS AND FLOW-CYTOMETRY IN PRIMARY BREAST-CANCER - RELATIONSHIP TO HORMONE RECEPTOR AND LYMPH-NODE STATUS [J].
COSTA, SD ;
KAUFMANN, M ;
FABBRO, D ;
TOKUS, M ;
FEICHTER, G ;
KLINGA, K ;
BASTERT, G .
GEBURTSHILFE UND FRAUENHEILKUNDE, 1989, 49 (04) :375-378
[9]   EXPRESSION OF SEVERAL GROWTH-FACTORS AND THEIR RECEPTOR GENES IN HUMAN COLON CARCINOMAS [J].
ITO, M ;
YOSHIDA, K ;
KYO, E ;
AYHAN, A ;
NAKAYAMA, H ;
YASUI, W ;
ITO, H ;
TAHARA, E .
VIRCHOWS ARCHIV B-CELL PATHOLOGY INCLUDING MOLECULAR PATHOLOGY, 1990, 59 (03) :173-178
[10]   TRANSFORMING GROWTH FACTORS(S) PRODUCTION ENABLES CELLS TO GROW IN THE ABSENCE OF SERUM - AN AUTOCRINE SYSTEM [J].
KAPLAN, PL ;
ANDERSON, M ;
OZANNE, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (02) :485-489