## Abstract A cell line derived from a normal beagle embryo was treated __in vitro__ with various levels of N‐methyl‐N′‐nitro‐N‐nitrosoguanidine or dimethyl sulfoxide (control). Cells treated only with the carcinogen underwent morphologic alteration __in vitro__, and one of these altered cell lines
Characterization of human cells transformed in vitro by n-methyl-n'-nitro-n-nitrosoguanidine
✍ Scribed by Johng S. Rhim; Donald L. Putman; Paul Arnstein; Robert J. Huebner; Robert M. McAllister
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- French
- Weight
- 791 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Human osteosarcoma (HOS) clonal cells transformed in vitro by N‐methyl‐N'‐nitro‐N‐nitroso‐guanidine (MNNG) were characterized, and compared to non‐producer HOS cells transformed by Kirsten murine sarcoma virus (Ki‐MSV). The MNNG‐ and virus‐transformed cells grew in the aggregate form above an agar base, grew in soft agar, and had a high fibrinolytic activity. When inoculated into nude mice, all the chemically or virally altered cells produced tumors or tumor nodules. When transplanted into ATS‐treated hamsters, the cells transformed by MNNG (0.01 μg/ml) and Ki‐MSV produced tumors but MNNG (0.1 μg/ml) transformed cells did not produce tumors. The control HOS cells did not grow in the aggregate form but formed colonies in soft agar, and had low fibrinolytic activity and no capacity to form tumors in nude mice and ATS‐treated hamsters. However, one of the control clonal lines had a high level of fibrinolytic activity. Cellular aggregation properties of human transformed cells did appear to correlate with tumorigenicity in nude mice.
📜 SIMILAR VOLUMES
## Abstract Using an organ culture/cell culture system, we transformed rat tracheal epithelial cells __in vitro__ by exposure to MNNG. Ten tracheal organ cultures per group were exposed twice (at days 3 and 6) to 0,0.001, 1.0 or 10.0 μg MNNG/ml of medium. Following this exposure, the explants were
## Abstract We have shown previously that exposure to a low concentration of __N__‐methyl‐__N__′‐nitro‐__N__‐nitrosoguanidine (MNNG) induces comprehensive changes in the protein expression profile of human amnion FL cells, including the induction, suppression, upregulation, and downregulation of va
Normal dog gallbladder epithelial cells in long-term culture were used as a model to study the morphologic, genetic, and secretory processes associated with the progression to cancer formation. Dog gallbladder epithelial cells cultured on collagen-coated plates grew into polarized monolayers, could
The effect of tyrosine methyl ester (TME) on the incidence, number, and histological types of gastric cancers induced by N-methyl-N'-nitro-N-nitroroguanidine (MNNG) was investigated in male Wistar rats. Rats were subcutaneously given TME, 5 I 2 mg/kg body weight, every other day after 20 weeks of or