The gene expression of human type I procollagen was investigated in cirrhotic human liver by using in situ hybridization with nonradioactive DNA probes. Using in situ hybridization can provide direct evidence for the cell type capable for type I collagen synthesis in tissues. T-T dimerized DNA probe
Expression of TGF-β and procollagen type I and type III in human gastric carcinomas
✍ Scribed by Kazuhiro Yoshida; Hiroshi Yokozaki; Minoru Niimoto; Hisao Ito; Masanori Ito; Eiichi Tahara
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- French
- Weight
- 940 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0020-7136
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✦ Synopsis
To elucidate the difference between xirrhous and nonxirrhous gastric Carcinomas, we examined the expressions of TGF-P, procollagen type I and type 111 in 7 gastric carcinoma cell lines and 37 gastric carcinoma tissues, and also examined the effect of TGF-P on the expression of procollagen mRNA by TMK-I cells. TGF-P mRNA was detected in all the tumors examined in vivo and in vitro. Interestingly, 9 (90%) of 10 scirrhous gastric carcinomas revealed higher levels of TGF-P mRNA than normal tissues, while 8 (38%) of 21 welldifferentiated adenocarcinomas had higher TGF-P mRNA levels than normal tissues. As for procollagen mRNA, most of the human gastric carcinoma cell lines expressed type-I procollagen mRNA and MKN-I expressed type-Ill procollagen mRNA. Furthermore, procollagen type-I mRNA accumulation in TMK-I cells was increased by exogenous TGF-P. Most of the tumor tissues from surgical specimens expressed higher procollagen mRNA than normal tissues. These results indicate that TGF-P produced by carcinoma cells might stimulate collagen synthesis not only by fibroblasts but also by carcinoma cells themselves, leading to diffuse fibrosis of scirrhous gastric carcinomas.
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