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Analytical Cellular Pathology
Volume 18, Issue 2, Pages 103-108
http://dx.doi.org/10.1155/1999/182468

Heterogeneity of DNA Distribution in Diploid Cells: A New Predicitive Discriminant Factor for Solid Tumour Behaviour

Jacques Assailly,1 Arnaud Desgrippes,2 Brigitte Loridon‐Rosa,3 Dominique Piron,3 Roger Dachez,4 and Daniel Beurton2

1A.I.P.C. Laboratoire d’Analyse d’Images en Pathologie Cellulaire, Centre HAYEM, Hôpital Saint Louis, 1 ave C. Vellefaux, 75475 Paris Cedex 10, France
2Service d’Urologie, Hôpital Ambroise PARE, 92100 Boulogne, France
3Centre de Pathologie, 19 rue de Passy, 75016 Paris, France
4Institut A. Fournier, 24 Bd Saint Jacques, 75014 Paris, France

Received 6 July 1998; Revised 28 January 1999; Accepted 27 March 1999

Copyright © 1999 Hindawi Publishing Corporation. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Spatial nuclear DNA heterogeneity distribution of Feulgen‐stained DNA diploid cells was studied by image cytometry in voided urine of 119 patients without bladder tumour (n=20) and with initial (n=23) or previous (n=76) diagnosed bladder tumour. For each patient, repetitive DNA measurements were performed during 1–4 years of follow up. Only cells of diploid DNA histograms and diploid subpopulations of aneuploid DNA histograms were used for analysis. DNA heterogeneity distribution of these diploid cells was quantified by statistical parameters of each nuclear optical density distribution. Discriminant analysis was performed on three groups of DNA histograms. Group A (n=44): aneuploid DNA histograms of patients with bladder tumour. Group D (n=55): 38 diploid DNA histograms of the 20 patients without bladder tumour (subgroup D1) and 17 diploid DNA histograms of patients with a non‐recurrent bladder tumour (subgroup D2). Group R (n=27): diploid DNA histograms of patients with bladder tumour recurrence. No statistically significant discriminant function was found to separate D1 and D2. However, the first canonical discriminant function C1 differentiated diploid cells of diploid DNA histograms (group D and group R) from diploid cell subpopulations of aneuploid DNA histograms (group A). Mean C1 values were 1.06, 0.84 and –1.45 for groups R, D and A, respectively. The second canonical discriminant function C2 differentiated diploid DNA histograms of patients with bladder tumour recurrence (group R) from diploid DNA histograms of patients without bladder tumour or without bladder tumour recurrence (group D). Mean C2 values were 1.78 and –0.76 for groups R and D, respectively. In 95% confidence limit, the rate of rediscrimination using the two first canonical discriminant functions C1 and C2 were 86.4, 74.5 and 74.1% for groups A, D and R, respectively. Percent of “grouped” cases correctly classified was 78.6%. Thus spatial DNA heterogeneity distribution of diploid cells seems to quantitate probable genetic instability as a function of clinical evolution such as tumour recurrence, and suggests the possible presence of aneuploid stemlines in a heterogeneous tumour, even if a diploid DNA histogram is observed in a single sample. From standardized C1 and C2 canonical discriminant function coefficients, a DNA heterogeneity index (2c‐HI) is proposed to characterize diploid cells providing a descriptive and predictive discriminant factor for solid tumour behaviour.