To evaluate the application of Ha-ras mRNA antisense oligonucleotide therapy for liver tumors, we examined the frequency and types of mutation in codon 61 of the Ha-ras oncogene in preneoplastic lesions and hepatocellular carcinomas induced by N-nitrosomorpholine (NNM) in rats. Thirtyseven percent o
Inhibition by retinoic acid of hepatocarcinogenesis induced by N-nitrosomorpholine and of expression of myc oncogene protein in sprague-dawley rats
β Scribed by Miyako Baba; Hiroyasu Iishi; Reiko Yamamoto; Masaharu Tatsuta
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- French
- Weight
- 429 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0020-7136
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β¦ Synopsis
The effects of all-trans-retinoic acid (RA) on hepato-carcinogenesis induced by N-nitrosomorpholine (NNM) and on the expression of rnyc p I10 proteins were investigated in male Sprague-Dawlay rats. Rats received i.m. injections of RA twice a week and, from the beginning of the experiment, were given drinking water containing NNM for 8 weeks. Pre-neoplastic and neoplastic lesions staining positively for gamma-glutamyl transpeptidase (GGT), glutathione-S-transferase placental type (GST-P) or rnyc pl10 protein were examined histochemically.
At week 18, quantitative histological analysis showed that prolonged administration of RA resulted in a significant reduction in the number, size and volume of GGT-positive and GST-P-positive hepatic lesions. Administration of RA also caused a significant increase in the proportion of myc p l 10-negative lesions to the total pre-neoplastic lesions observed. Myc p I IOnegative lesions had a significantly lower mitotic index than rnyc p l 10-positive lesions. These findings indicate that RA inhibits hepatocarcinogenesis and suggest that this effect may be related to its influence in reducing the expression of rnyc gene proteins and its subsequent inhibition of cell proliferation in pre-neoplastic lesions.
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