Flow Cytometric DNA Patterns in Cervical Carcinoma

Authors

  • P. Strang Department of Oncology and Pathology, Akademiska Sjukhuset, University of Uppsala, S-75185, Uppsala; The Department of Gynecologic Oncology, University Hospital, S-90185, Umea; The Department of Gynecologic Oncology, Orebro Medical Center, s-70185, Orebro, Sweden
  • U. Stendahl Department of Oncology and Pathology, Akademiska Sjukhuset, University of Uppsala, S-75185, Uppsala; The Department of Gynecologic Oncology, University Hospital, S-90185, Umea; The Department of Gynecologic Oncology, Orebro Medical Center, s-70185, Orebro, Sweden
  • B. Frankendal Department of Oncology and Pathology, Akademiska Sjukhuset, University of Uppsala, S-75185, Uppsala; The Department of Gynecologic Oncology, University Hospital, S-90185, Umea; The Department of Gynecologic Oncology, Orebro Medical Center, s-70185, Orebro, Sweden
  • A. Lindgren Department of Oncology and Pathology, Akademiska Sjukhuset, University of Uppsala, S-75185, Uppsala; The Department of Gynecologic Oncology, University Hospital, S-90185, Umea; The Department of Gynecologic Oncology, Orebro Medical Center, s-70185, Orebro, Sweden

DOI:

https://doi.org/10.3109/02841868609136414

Keywords:

Uterine neoplasms, cervical cancer, flow cytometry, DNA

Abstract

low cytometric measurements of the DNA content were performed in a prospective study of 167 women with invasive squamous cell carcinoma of the uterine cervix. Ploidy level and the proportion of S-phase cells were correlated to age, menopausal age, staging according to FIGO and histopathology. With increasing age a successive shift from a dominance of peri-diploid and peri-tetraploid values to marked aneuploidy was found. Peridiploid and peri-tetraploid tumors were more often found in premenopausal than in post-menopausal women (p<0.001). The mean S-phase rate was significantly higher in women aged 60–89 years than in women aged 20–59 years (p<0.01). More aneuploid tumors were found in stages 111 and IV than in stages IB and 11 (p<0.01). The mean S-phase rate was higher in stages 111 and IV (20.8%) than in stages IB and 11 (17.2%) (p<0.01). No statistically significant correlation was shown between ploidy level and histopathology or between S-phase rate and histopathology. In 37 patients polyclonal tumors were found. The reproducibility of the method was good (r=0.99).

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Published

1986-01-01

How to Cite

Strang, P., Stendahl, U., Frankendal, B., & Lindgren, A. (1986). Flow Cytometric DNA Patterns in Cervical Carcinoma. Acta Oncologica, 25(4-6), 249–254. https://doi.org/10.3109/02841868609136414