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Neuroendocrine cells in serially passaged rat stomach cancers induced by MNNG
Abstract:
Five gastric carcinomas, induced in inbred Wistar rats by oral administration of N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) dissolved in drinking water, were successfully transplanted to isologous rats. The transplants grew to a size of 10 to 35 mm in diameter within 8 to 25 weeks of implantation. In one case, serial transplantation were maintained up to the 11th generation, with occurrence of distant metastasis in the 3rd generation. Histological histochemical, and electron microscopical comparison of the original and transplanted tumors revealed that (1) the original tumors were quite well differentiated, forming either papillary or tubular structures, whereas the transplants were more anaplastic and pleomorphic showing often solid nests; and (2) tumor cells with gastrointestinal differentiation and cells with neuroendocrine differentiation were present and evenly distributed in both the original and the serially transplanted tumors. As it is unlikely that the normal and neoplastic neuroendocrine cells are growing side-by-side with and independently of the epithelial neoplastic components in the present series of transplants, the findings strongly suggest (1) the multidirectional potency of the inbred rat stomach carcinoma cells and (2) the common neoplastic origin of the epithelial and neuroendocrine components.
Insights
Transplanted rat stomach carcinomas, induced by N-methyl-N'-nitro-N-nitrosoguanidine (MNNG), showed multidirectional cell potency. Both epithelial and neuroendocrine components likely originated from a common neoplastic source.
Area of Science:
- Oncology
- Gastroenterology
- Cell Biology
Background:
- Gastric carcinomas can arise from various cell types.
- Understanding tumor cell plasticity is crucial for cancer research.
Purpose of the Study:
- To investigate the transplantability and cellular characteristics of chemically induced rat gastric carcinomas.
- To explore the potential for multidirectional differentiation in gastric carcinoma cells.
Main Methods:
- Induction of gastric carcinomas in Wistar rats using N-methyl-N itro-N-nitrosoguanidine (MNNG).
- Successful transplantation of tumors to isologous rats.
- Serial transplantation up to the 11th generation.
- Histological, histochemical, and electron microscopic analysis of original and transplanted tumors.
Main Results:
- Transplanted tumors grew successfully, with metastasis observed in one case.
- Original tumors were well-differentiated, while transplants became more anaplastic.
- Both epithelial and neuroendocrine tumor cells were present in original and transplanted tumors, suggesting a common origin.
Conclusions:
- Inbred rat stomach carcinoma cells exhibit multidirectional differentiation potential.
- Epithelial and neuroendocrine components of these tumors likely share a common neoplastic origin.