We explored the potential therapeutic benefit of introducing GM-CSF, IFN-β₯ or a combination of both factors into CT26 tumor cells. CT26 cells secreting either GM-CSF or IFN-β₯ exhibited delayed tumorigenicity; however, cells expressing both GM-CSF and IFN-β₯ did not form tumors. Even when wild type CT
A correlation between GM-CSF gene expression and metastases in murine tumors
β Scribed by Kazuyoshi Takeda; Kohki Hatakeyama; Yoshinori Tsuchiya; Hidemi Rikiishi; Katsuo Kumagai
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- French
- Weight
- 1007 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
β¦ Synopsis
Using 14 transplantable murine tumors, we investigated a possible correlation between their ability to produce the cytokine GM-CSF and the spontaneous metastatic potential when mice were subcutaneously inoculated. The following results were obtained: (I) seven tumors, which produced severe pulmonary metastases and metastatic swelling of lymph nodes, exhibited the ability to produce GM-CSF activity in culture. The cell population analysis revealed that the cells producing GM-CSF were tumor cells themselves, but that contaminating macrophagedgranulocytes and T lymphocytes did not produce GM-CSF. The mRNA for GM-CSF was also found in all of these highly metastatic tumors tested. In mice inoculated with a highly metastatic tumor, the GM-CSF mRNA was also found in lungs; (2) in 3 other tumors, which produced histological but not macroxopical pulmonary rnetastases, no GM-CSF activity could be detected in the culture fluids. GM-CSF mRNA was, however, detected in the tumor cells in the presence of an mRNA-stabilizing agent, cyclohexhide, suggesting the possibility that the tumor cells of this type were transcribing GM-CSF gene, and secreting it in undetectable levels; (3) in culture of the 4 remaining poorly or non-metastatic tumors, neither CSF activity nor GM-CSF mRNA could be detected even in the presence of cycloheximide. GM-CSF mRNA was also not found in lungs of tumorbearing mice. Our results indicate that there may be a correlation between GM-CSF gene expression in tumor cells and spontaneous metastases.
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