A new mouse tumor model system (RIF-1) for comparison of end-point studies

P. R. Twentyman, J. M. Brown, J. W. Gray, A. J. Franko, M. A. Scoles, R. F. Kallman

Research output: Contribution to journalArticlepeer-review

414 Scopus citations

Abstract

A new tumor model system (RIF-1) was developed that is very suitable for studies in which clonogenic survival is compared with growth delay and control probability following various forms of treatment. The tumor was a radiation-induced sarcoma in the inbred female C3H/Km mouse. It had a low median tumor dose, had a satisfactory plating efficiency direct from in vivo to in vitro, was nonimmunogenic or minimally immunogenic, and metastasized only at a relatively advanced stage of growth. The cell line grew either as a monolayer on plastic dishes, as tumor spheroids in spinner culture, as lung nodules following injection of a single-cell suspension into the tail veins of syngeneic mice, or as a solid tumor. Both diploid and tetraploid clonogenic cells were found in monolayer cultures of the RIF-1 line.

Original languageEnglish (US)
Pages (from-to)595-604
Number of pages10
JournalJournal of the National Cancer Institute
Volume64
Issue number3
StatePublished - May 2 1980

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

Fingerprint Dive into the research topics of 'A new mouse tumor model system (RIF-1) for comparison of end-point studies'. Together they form a unique fingerprint.

Cite this