GENETIC INSTABILITY COUPLED TO CLONAL SELECTION AS A MECHANISM FOR TUMOR PROGRESSION IN THE DUNNING R-3327 RAT PROSTATIC ADENOCARCINOMA SYSTEM

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  • 1 January 1982
    • journal article
    • research article
    • Vol. 42  (6) , 2353-2361
Abstract
The androgen-sensitive Dunning R-3327-H prostatic adenocarcinoma has been maintained by continuous serial passage in intact male rats for many years. While it has been possible to maintain the original characteristics of the well-differentiated H tumor over 16 yr, there have evolved spontaneously more aberrant sublines from this tumor at several subpassages in intact male rats. Serial passage of these individual sublines has established 5 additional R-3327 tumors each with distinct phenotypes and each more aberrant than the parent H tumor. By passage of the H tumor in castrated male rats, it was possible to obtain a well-differentiated slow-growing androgen-insensitive tumor termed the HI-S tumor. The continuous serial passage of this HI-S tumor has resulted in the emergence of 3 new types of Dunning tumors. Results from biochemical and chromosomal studies demonstrate that there is a consistent association in each of these tumor progressions between the expression of genetic instability, which results in the addition of phenotypically new clones of cells to the tumor population, and the subsequent selection of these newly developed clones. The process of genetic instability coupled to clonal selection is one mechanism for the change in tumor phenotype characteristically associated with tumor progression within this system of prostatic tumors.