High-molecular-weight genomic DNA isolated from a human cutaneous squamous cell carcinoma (AS) was assayed for its ability to induce tumorigenic transformation of NIH 3T3 cells. Subcutaneous injection of NIH 3T3 cells cotransfected with DNAs from AS tumor and pSV2-neo plasmid not only induced tumors
Production of the metastatic phenotype by DNA transfection in a rat mammary model.
β Scribed by Barry R. Davies; Roger Barraclough; Michael P.A. Davies; Philip S. Rudland
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- English
- Weight
- 587 KB
- Volume
- 17
- Category
- Article
- ISSN
- 1065-6995
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
A syngeneic, immunocompetent rat mammary model has been employed to investigate the molecular basis of the metastatic phenotype. Transfection of the benign rat mammary epithelial cell line Rama 37 with the gene for p9Ka; a small, rat, calciumβbinding protein or DNA from metastatic human cell lines derived from a primary breast carcinoma or a pleural effusion yields transfectants with metastatic capabilities. Transfection of DNA from a benign human mammary cell line, a plasmid containing a cDNA for the human basic fibroblast growth factor (bFGF) gene, or the oncogene EJβrasβ1, fails to yield any transfectants expressing the metastatic phenotype.
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