Abstract
Dunning R3327-H rat prostate adenocarcinoma cells, when grown in syngeneic (Copenhagen) rats or nude mice, produce tumors with prominent hypercellular stroma. The authors have previously demonstrated the presence of anomalous steroid-sensitive cells in both the epithelium and stromal compartments of this model system. In order to better understand the histogenesis of these cells, the authors studied samples of the tumor which were radiolabeled overnight with tritiated dihydrotestosterone (3H-DHT). Frozen sections of the tissues were thaw-mounted onto autoradiographic emulsion-coated slides to permit silver grain identification in association with nuclei of androgen-sensitive cells. Surprisingly, numerous silver grains were found to be associated with nuclei of large cells within the stroma. Therefore, these cells were termed "epithelioid" pending confirmation of their origin. To further define these cells and their relationship to the surrounding matrix, autoradiograms have now been examined immunohistochemically with antibodies directed against the basement membrane glycoprotein, laminin, as well as antibodies specific for intermediate cytoskeletal filaments. Following identification of acinar basement membranes, epithelioid cells were identifiable both in the stroma and in the acinar epithelial cell layer. Histochemical staining with acid phosphatase, a marker for prostatic epithelium, was performed and shown to be present in acinar epithelial cells as well as in epithelioid cells. Additionally, fluorescence-activated cell sorting was employed to characterize the DNA content of cell types within the H tumor. Epithelioid cells were found to be in highest concentration in an aneuploid peak with a ploidy of approximately 6N. The autoradiographic, immunohistochemical, cytometric, and ultramicroscopic studies suggest that 1) epithelioid cells are epithelial derived stromal cells; 2) these epithelioid cells arise by pathologic division of aneuploid neoplastic precursor cells of approximately 3N ploidy, which are found within the prostatic epithelium; and 3) the resulting 6N cells degrade the basement membrane locally, invade the stroma, and populate it. Here, they can be distinguished from fibroblasts by their size, acid phosphatase activity, and hormone receptor content. Thus, the term "epithelioid" is inappropriate; and these cells should be regarded simply as large neoplastic epithelial (LNE) cells. The presence of this cell type suggests that this tumor subline represents a useful naturally occurring model for the study of the initial stages of neoplastic transformation.
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- Barsky S. H., Siegal G. P., Jannotta F., Liotta L. A. Loss of basement membrane components by invasive tumors but not by their benign counterparts. Lab Invest. 1983 Aug;49(2):140–147. [PubMed] [Google Scholar]
- Beckman W. C., Jr, Jacokes A. L., Camps J. L., Jr, Cook R. L., Siegal G. P. Analysis of changes in rat prostate carcinoma following hormone deprivation. Am J Pathol. 1987 Sep;128(3):566–572. [PMC free article] [PubMed] [Google Scholar]
- Beckman W. C., Jr, Mickey D. D., Fried F. A. Autoradiographic localization of estrogen and androgen target cells in human and rat prostate carcinoma. J Urol. 1985 Apr;133(4):724–728. doi: 10.1016/s0022-5347(17)49170-1. [DOI] [PubMed] [Google Scholar]
- Benson M. C., McDougal D. C., Coffey D. S. The use of multiparameter flow cytometry to assess tumor cell heterogeneity and grade prostate cancer. Prostate. 1984;5(1):27–45. doi: 10.1002/pros.2990050104. [DOI] [PubMed] [Google Scholar]
- Claflin A. J., Pollack A., Malinin T., Block N. L., Irvin G. L. Flow cytometric analysis of R3327 rat prostate adenocarcinoma grown in vivo and in vitro. J Natl Cancer Inst. 1982 Jul;69(1):79–87. [PubMed] [Google Scholar]
- DUNNING W. F. PROSTATE CANCER IN THE RAT. Natl Cancer Inst Monogr. 1963 Oct;12:351–369. [PubMed] [Google Scholar]
- Isaacs J. T., Heston W. D., Weissman R. M., Coffey D. S. Animal models of the hormone-sensitive and -insensitive prostatic adenocarcinomas, Dunning R-3327-H, R-3327-HI, and R-3327-AT. Cancer Res. 1978 Nov;38(11 Pt 2):4353–4359. [PubMed] [Google Scholar]
- Isaacs J. T., Isaacs W. B., Coffey D. S. Models for development of nonreceptor methods for distinguishing androgen-sensitive and -insensitive prostatic tumors. Cancer Res. 1979 Jul;39(7 Pt 1):2652–2659. [PubMed] [Google Scholar]
- Isaacs J. T., Wake N., Coffey D. S., Sandberg A. A. Genetic instability coupled to clonal selection as a mechanism for tumor progression in the Dunning R-3327 rat prostatic adenocarcinoma system. Cancer Res. 1982 Jun;42(6):2353–2371. [PubMed] [Google Scholar]
- Isaacs J. T., Yu G. W., Coffey D. S. The characterization of a newly identified, highly metastatic variety of Dunning R 3327 rat prostatic adenocarcinoma system: the MAT LyLu tumor. Invest Urol. 1981 Jul;19(1):20–23. [PubMed] [Google Scholar]
- Keefer D. A., Stumpf W. E., Petrusz P. Quantitative autoradiographic assessment of 3H-estradiol uptake in immunocytochemically characterized pituitary cells. Cell Tissue Res. 1976 Feb 6;166(1):25–35. doi: 10.1007/BF00215122. [DOI] [PubMed] [Google Scholar]
- Lazan D. W., Heston W. D., Kadmon D., Fair W. R. Inhibition of the R3327MAT-Lu prostatic tumor by diethylstilbestrol and 1,2-bis(3,5-dioxopiperazin-1-yl)propane. Cancer Res. 1982 Apr;42(4):1390–1394. [PubMed] [Google Scholar]
- Lea O. A., French F. S. Androgen receptor protein in the androgen-dependent Dunning R-3327 prostate carcinoma. Cancer Res. 1981 Feb;41(2):619–623. [PubMed] [Google Scholar]
- Markland F. S., Chopp R. T., Cosgrove M. D., Howard E. B. Characterization of steroid hormone receptors in the Dunning R-3327 rat prostatic adenocarcinoma. Cancer Res. 1978 Sep;38(9):2818–2826. [PubMed] [Google Scholar]
- Markland F. S., Chopp R. T., Cosgrove M. D., Howard E. B. Steroid hormone receptor characterization of several histologic variants of a rat prostatic adenocarcinoma. J Supramol Struct. 1978;9(4):509–524. doi: 10.1002/jss.400090406. [DOI] [PubMed] [Google Scholar]
- Miettinen M., Franssila K., Lehto V. P., Paasivuo R., Virtanen I. Expression of intermediate filament proteins in thyroid gland and thyroid tumors. Lab Invest. 1984 Mar;50(3):262–270. [PubMed] [Google Scholar]
- Mobbs B. G., Johnson I. E. Characterization of estrogen-induced progestin binding in cytosol of the R3327 prostatic carcinoma of the rat. J Steroid Biochem. 1985 Jan;22(1):57–62. doi: 10.1016/0022-4731(85)90141-4. [DOI] [PubMed] [Google Scholar]
- Moll R., Moll I., Franke W. W. Differences of expression of cytokeratin polypeptides in various epithelial skin tumors. Arch Dermatol Res. 1984;276(6):349–363. doi: 10.1007/BF00413355. [DOI] [PubMed] [Google Scholar]
- Ordronneau P., Lindström P. B., Petrusz P. Four unlabeled antibody bridge techniques: a comparison. J Histochem Cytochem. 1981 Dec;29(12):1397–1404. doi: 10.1177/29.12.7033366. [DOI] [PubMed] [Google Scholar]
- Sestili M. A., Norris J. S., Lipschultz L. I., Smith R. G. Dunning adenocarcinoma in tissue culture: isolation of a cloned cell line, R3327H-G8-A1. J Urol. 1982 Apr;127(4):823–825. doi: 10.1016/s0022-5347(17)54058-6. [DOI] [PubMed] [Google Scholar]
- Shapiro H. M. Flow cytometric estimation of DNA and RNA content in intact cells stained with Hoechst 33342 and pyronin Y. Cytometry. 1981 Nov;2(3):143–150. doi: 10.1002/cyto.990020302. [DOI] [PubMed] [Google Scholar]
- Smolev J. K., Heston W. D., Scott W. W., Coffey D. S. Characterization of the Dunning R3327H prostatic adenocarcinoma: an appropriate animal model for prostatic cancer. Cancer Treat Rep. 1977 Mar-Apr;61(2):273–287. [PubMed] [Google Scholar]
- Stonington O. G., Szwec N., Webber M. Isolation and identification of the human malignant prostatic epithelial cell in pure monolayer culture. J Urol. 1975 Dec;114(6):903–908. doi: 10.1016/s0022-5347(17)67171-4. [DOI] [PubMed] [Google Scholar]
- Strobl J. S., Monaco M. E., Lippman M. E. The role of intracellular equilibria and the effect of antiestrogens on estrogen-receptor dissociation kinetics from perfused cultures of human breast cancer cells. Endocrinology. 1980 Aug;107(2):450–460. doi: 10.1210/endo-107-2-450. [DOI] [PubMed] [Google Scholar]
- Stumpf W. E., Sar M. Autoradiographic techniques for localizing steroid hormones. Methods Enzymol. 1975;36:135–156. doi: 10.1016/s0076-6879(75)36016-3. [DOI] [PubMed] [Google Scholar]
- Vogel A. M., Gown A. M., Caughlan J., Haas J. E., Beckwith J. B. Rhabdoid tumors of the kidney contain mesenchymal specific and epithelial specific intermediate filament proteins. Lab Invest. 1984 Feb;50(2):232–238. [PubMed] [Google Scholar]
- Voigt W., Dunning W. F. In vivo metabolism of testosterone-3H in R-3327, an androgen-sensitive rat prostatic adenocarcinoma. Cancer Res. 1974 Jun;34(6):1447–1450. [PubMed] [Google Scholar]
- Voigt W., Feldman M., Dunning W. F. 5alpha-dihydrotestosterone-binding proteins and androgen sensitivity in prostatic cancers of Copenhangen rats. Cancer Res. 1975 Jul;35(7):1840–1846. [PubMed] [Google Scholar]












