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Pulse cytometric analysis of the perturbed cellular kinetics of solid tumors: problems and promises

Conference ·
OSTI ID:7204293
Pulse cytometric measurements of the cellular DNA content distributions have been made on cells from normal and hydroxyurea-perturbed mammary tumors from two in vivo lines (Slow and S102F) of the C3H mouse. The tumor cells were dissociated mechanically and stained for DNA according to an acriflavine-Feulgen technique. A comparison of autoradiographic data from the tumor sections and single cell suspensions following pulse labeling with /sup 3/H-TdR showed that the dissociation technique is not biased against cells from any of the various phases of the cell cycle; however the mitotic cells are difficult to recognize morphologically. The fluorescence distributions from the DNA stained cells showed a peak corresponding to noncycling diploid cells and at a higher fluorescence, a classical distribution of cycling tumor cells which are near-tetraploid in DNA content. These features are superimposed on a continuum of fluorescence from stained cellular and nuclear fragments. The changes in the DNA distributions produced by perturbing the tumors with hydroxyurea are compared through mathematical modeling to those expected from kinetic data obtained by the more classical methodology of /sup 3/H-TdR pulse labeling and autoradiography. Both the flow microfluorometric and autoradiographic data show that a single injection of hydroxyurea affects a sizable fraction of the S102F tumor cells. The effects on the Slow tumor cells are not as readily apparent. (auth)
Research Organization:
California Univ., Livermore (USA). Lawrence Livermore Lab.
DOE Contract Number:
W-7405-ENG-48
OSTI ID:
7204293
Report Number(s):
UCRL-77458; CONF-750957-4
Country of Publication:
United States
Language:
English