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Relationship between intrinsic radiation sensitivity and metastatic potential
1Department of Radiation Oncology and the Massachusetts General Hospital, Harvard Medical School, Boston 02114, USA.
International Journal of Radiation Oncology, Biology, Physics
|January 1, 1996
Summary
This study found a strong correlation between cancer cell radiation resistance and their ability to metastasize. Oncogenes like ras and myc increased both radiation resistance and metastatic potential in rat embryo cells.
Area of Science:
- Oncogene research
- Cancer biology
- Radiobiology
Background:
- Previous research focused on oncogene-induced changes in tumor formation and metastasis.
- The relationship between intrinsic cellular radiation sensitivity and metastatic potential remained unexplored.
Purpose of the Study:
- To investigate the correlation between intrinsic radiation sensitivity and experimental metastatic potential in oncogene-transfected rat embryo cells (REC).
Main Methods:
- Rat embryo cells were transfected with oncogenes (ras, v-myc, E1a) and their combinations.
- In vitro radiation sensitivity was assessed using clonogenic assays (SF2, MID).
- Tumorigenicity and experimental metastatic potential (lung colonization) were evaluated in vivo.
Main Results:
- REC, mock-transfected REC, E1a, and E1a/ras transfectants showed similar radiation sensitivity.
- Ras and ras/myc transfected cells exhibited increased radiation resistance (p <0.05).
- Ras and ras/myc transfectants demonstrated significant experimental metastatic potential, while E1a/ras transfectants were tumorigenic but poorly metastatic.
Conclusions:
- A significant correlation exists between intrinsic radiation sensitivity and experimental metastatic potential in transfected REC.
- Activated ras alone or in combination with v-myc conferred the highest radiation resistance and metastatic potential.
- E1a/ras cotransfected cells, though tumorigenic, were relatively radiation-sensitive and nonmetastatic, suggesting complex oncogenic pathway interactions.