Gastric cancer induced by N-methyl-N’-nitro-N-nitrosoguanidine in rat with ulcers and expressions of ras and c-erbB2 genes
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Gastric cancer induced by N-methyl-N’-nitro-N-nitrosoguanidine in rat with ulcers and expressions of ras and c-erbB2 genes
Gastric cancer induced by N-methyl-N’-nitro-N-nitrosoguanidine in rat with ulcers and expressions of ras and c-erbB2 genes
解放军医学杂志(英文版)2003年第1期 页码:8-10
Affiliations:
1. Department of Pharmacy
2. Zhujiang Hospital
3. First Military Medical University
4. Piwei Institute
5. Guangzhou University of Traditional Chinese Medicine
6. Guangzhou University of Traditional Chinese Medicine Guangzhou,510282
7. ,Guangzhou,510407
Author bio:
Funds:
DOI:
中图分类号:R735.2
纸质出版:2003
Accepted:
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Gastric cancer induced by N-methyl-N’-nitro-N-nitrosoguanidine in rat with ulcers and expressions of ras and c-erbB2 genes[J]. 解放军医学杂志(英文版), 2003,(1):8-10.
[1]周本杰,陈蔚文,徐勤,李茹柳,王建华.Gastric cancer induced by N-methyl-N'-nitro-N-nitrosoguanidine in rat with ulcers and expressions of ras and c-erbB2 genes[J].Journal of Medical Colleges of PLA,2003(01):8-10.
Gastric cancer induced by N-methyl-N’-nitro-N-nitrosoguanidine in rat with ulcers and expressions of ras and c-erbB2 genes[J]. 解放军医学杂志(英文版), 2003,(1):8-10.DOI:
[1]周本杰,陈蔚文,徐勤,李茹柳,王建华.Gastric cancer induced by N-methyl-N'-nitro-N-nitrosoguanidine in rat with ulcers and expressions of ras and c-erbB2 genes[J].Journal of Medical Colleges of PLA,2003(01):8-10.DOI:
Gastric cancer induced by N-methyl-N’-nitro-N-nitrosoguanidine in rat with ulcers and expressions of ras and c-erbB2 genes
摘要
Abstract
<正> Objective: To observe the series of pathological changes during the development of gastric adenocarcinoma in ulcerative rats induced by N-methyl-N’-nitro-N-nitrosoguanidine (MNNG)
and the expression profile of related on-cogenic protein. Methods: MNNG was administered in rats with ulcers due to acetic acid treatment to induce gastric cancer
and the protein expressions of ras and c-erbB2 genes in the ulcer were examined immunohistochemically along with pathological examination. Results: The incidence of gastric adenocarcinoma in the model group reaches 40% (6/ 15)
while none of the rats developed cancer in the control group with ulcers. Positive expressions of the proteins of p21ras and c-erbB2 were observed in the tissues undergoing canceration in the 6 rats of model group
but were not observed in the 5 control rats; p53 protein expression
however
failed to be detected in both groups. Conclusion: A new animal model of gastric cancer has been established in rats with gastric ulcer after MNNG trea
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