Cytotoxic effects of TGF-alpha-Pseudomonas exotoxin A fusion protein in human pancreatic carcinoma cells

被引:11
作者
Baldwin, RL
Kobrin, MS
Tran, T
Pastan, I
Korc, M
机构
[1] UNIV CALIF IRVINE,DEPT MED,DIV ENDOCRINOL DIABET & METAB MED SCI 1,IRVINE,CA 92717
[2] UNIV CALIF IRVINE,DEPT BIOL CHEM,IRVINE,CA 92717
[3] NCI,MOLEC BIOL LAB,NIH,BETHESDA,MD 20892
关键词
TP40; growth inhibition; epidermal growth factor receptor;
D O I
10.1097/00006676-199607000-00002
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The epidermal growth factor (EGF) receptor is overexpressed in human pancreatic cancers and cultured cell lines. TP40 is a chimeric protein composed of transforming growth factor-alpha (TGF-alpha) linked to a modified Pseudomonas exotoxin A (PE40) that exerts growth inhibitory effects on cells bearing a high number of EGF receptors. Therefore, we compared the effect of TP40 on the growth of Chinese hamster ovary (CHO) cells expressing varying levels of the EGF receptor and on the growth of two human pancreatic cancer cell lines. The growth of CHO cells devoid of endogenous EGF receptors was minimally altered by high concentrations of TP40, even following a 72-h incubation period. In contrast, in CHO cells expressing similar to 95,000 and 438,000 EGF receptors per cell, one-half maximal growth inhibition occurred at 5 and 3 ng/ml TP40, respectively. Following a 72-h incubation in T3M4 and COLO 357 human pancreatic cancer cells, one-half maximal growth inhibition occurred at 0.2 and 0.4 ng/ml TP40, respectively. This effect was significantly greater than that of native Pseudomonas exotoxin A. These findings indicate that human pancreatic cancer cells are markedly sensitive to the growth inhibitory effects of TP40 and raise the possibility that TP40 may have a therapeutic role in this disorder.
引用
收藏
页码:16 / 21
页数:6
相关论文
共 37 条
[1]   ACTIVITY OF A RECOMBINANT FUSION PROTEIN BETWEEN TRANSFORMING GROWTH-FACTOR TYPE-ALPHA AND PSEUDOMONAS TOXIN [J].
CHAUDHARY, VK ;
FITZGERALD, DJ ;
ADHYA, S ;
PASTAN, I .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (13) :4538-4542
[2]   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
[3]  
EBERT M, 1994, CANCER RES, V54, P3959
[4]   CYTOTOXIC EFFECTS OF A RECOMBINANT CHIMERIC TOXIN ON RAPIDLY PROLIFERATING VASCULAR SMOOTH-MUSCLE CELLS [J].
EPSTEIN, SE ;
SIEGALL, CB ;
BIRO, S ;
FU, YM ;
FITZGERALD, D ;
PASTAN, I .
CIRCULATION, 1991, 84 (02) :778-787
[5]  
FARAHBAKHSH ZT, 1986, J BIOL CHEM, V261, P1404
[6]   USE OF MTT COLORIMETRIC ASSAY TO MEASURE CELL ACTIVATION [J].
GERLIER, D ;
THOMASSET, N .
JOURNAL OF IMMUNOLOGICAL METHODS, 1986, 94 (1-2) :57-63
[7]   CLONING, NUCLEOTIDE-SEQUENCE, AND EXPRESSION IN ESCHERICHIA-COLI OF THE EXOTOXIN-A STRUCTURAL GENE OF PSEUDOMONAS-AERUGINOSA [J].
GRAY, GL ;
SMITH, DH ;
BALDRIDGE, JS ;
HARKINS, RN ;
VASIL, ML ;
CHEN, EY ;
HEYNEKER, HL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (09) :2645-2649
[8]   RAPID COLORMETRIC ASSAY FOR CELL VIABILITY - APPLICATION TO THE QUANTITATION OF CYTO-TOXIC AND GROWTH INHIBITORY LYMPHOKINES [J].
GREEN, LM ;
READE, JL ;
WARE, CF .
JOURNAL OF IMMUNOLOGICAL METHODS, 1984, 70 (02) :257-268
[9]  
GUDJONSSON B, 1987, CANCER, V60, P2284, DOI 10.1002/1097-0142(19871101)60:9<2284::AID-CNCR2820600930>3.0.CO
[10]  
2-V