DNA Ploidy and S-Phase Fraction in Carcinoma of the Gallbladder Related to Histopathology, Number of Gallstones and Survival 1

Gallstones are a risk factor for the development of gallbladder cancer. We studied DNA ploidy and cell cycle composition by flow cytometry in archival specimens from 52 gall bladder carcinomas in relation to histopathological grade, tumour stage, gallstone number and survival. 69% of the gallbladder...

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Main Authors: Ulf Gustafsson, Curt Einarsson, Lennart C. Eriksson, Virgil Gadaleanu, Staffan Sahlin, Bernhard Tribukait
Format: Article
Language:English
Published: Wiley 2001-01-01
Series:Analytical Cellular Pathology
Online Access:http://dx.doi.org/10.1155/2001/469630
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author Ulf Gustafsson
Curt Einarsson
Lennart C. Eriksson
Virgil Gadaleanu
Staffan Sahlin
Bernhard Tribukait
author_facet Ulf Gustafsson
Curt Einarsson
Lennart C. Eriksson
Virgil Gadaleanu
Staffan Sahlin
Bernhard Tribukait
author_sort Ulf Gustafsson
collection DOAJ
description Gallstones are a risk factor for the development of gallbladder cancer. We studied DNA ploidy and cell cycle composition by flow cytometry in archival specimens from 52 gall bladder carcinomas in relation to histopathological grade, tumour stage, gallstone number and survival. 69% of the gallbladder carcinomas showed aneuploidy. All tumours with single stones (N=11) were aneuploid while only 61% of tumours with multiple stones (N=41) were aneuploid (p=0.002). DNA aneuploidy was related to increase in T‐category (p=0.01), grade (p=0.02), and nuclear pleomorphism (p=0.0005). The distribution of DNA ploidy shifted from tetraploid in low stage towards triploid positions in high stage tumours (p=0.02) combined with higher S‐phase values in triploid tumours (p=0.05). S‐phase fraction increased during development from normal tissue to dysplasia, cancer in situ and cancer in diploid cases (p=0.0002), and further at the change from diploid to aneuploid (p=0.004). At a median cancer specific survival time of four months patients with diploid tumours had a better survival than those with aneuploid tumours (p=0.02). In multivariate analysis of the tumour characteristic, only T‐category and tumour grade were independent prognostic factors. The shift from diploid to aneuploid and the further shift of ploidy within aneuploid tumours are in agreement with the concept of a clonal development of gallbladder cancer. These changes are combined with a stepwise increase in the fraction of S‐phase cells. Low frequency of symptoms in single stone patients may be the reason for detection of malignancy at a late stage of tumour development.
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spelling doaj-art-7bc96e50dd8844c1880bdcd6583754b62025-02-03T05:57:37ZengWileyAnalytical Cellular Pathology0921-89121878-36512001-01-01233-414315210.1155/2001/469630DNA Ploidy and S-Phase Fraction in Carcinoma of the Gallbladder Related to Histopathology, Number of Gallstones and Survival 1Ulf Gustafsson0Curt Einarsson1Lennart C. Eriksson2Virgil Gadaleanu3Staffan Sahlin4Bernhard Tribukait5Department of Surgery, Danderyd Hospital, SwedenCenter for Gastroenterology, Huddinge University Hospital, SwedenDepartment of Pathology, Huddinge University Hospital, SwedenDepartment of Pathology, Malmö University Hospital, SwedenDepartment of Surgery, Danderyd Hospital, SwedenDepartment of Medical Radiation Biology, Karolinska Hospital, Karolinska Institutet, Stockholm, SwedenGallstones are a risk factor for the development of gallbladder cancer. We studied DNA ploidy and cell cycle composition by flow cytometry in archival specimens from 52 gall bladder carcinomas in relation to histopathological grade, tumour stage, gallstone number and survival. 69% of the gallbladder carcinomas showed aneuploidy. All tumours with single stones (N=11) were aneuploid while only 61% of tumours with multiple stones (N=41) were aneuploid (p=0.002). DNA aneuploidy was related to increase in T‐category (p=0.01), grade (p=0.02), and nuclear pleomorphism (p=0.0005). The distribution of DNA ploidy shifted from tetraploid in low stage towards triploid positions in high stage tumours (p=0.02) combined with higher S‐phase values in triploid tumours (p=0.05). S‐phase fraction increased during development from normal tissue to dysplasia, cancer in situ and cancer in diploid cases (p=0.0002), and further at the change from diploid to aneuploid (p=0.004). At a median cancer specific survival time of four months patients with diploid tumours had a better survival than those with aneuploid tumours (p=0.02). In multivariate analysis of the tumour characteristic, only T‐category and tumour grade were independent prognostic factors. The shift from diploid to aneuploid and the further shift of ploidy within aneuploid tumours are in agreement with the concept of a clonal development of gallbladder cancer. These changes are combined with a stepwise increase in the fraction of S‐phase cells. Low frequency of symptoms in single stone patients may be the reason for detection of malignancy at a late stage of tumour development.http://dx.doi.org/10.1155/2001/469630
spellingShingle Ulf Gustafsson
Curt Einarsson
Lennart C. Eriksson
Virgil Gadaleanu
Staffan Sahlin
Bernhard Tribukait
DNA Ploidy and S-Phase Fraction in Carcinoma of the Gallbladder Related to Histopathology, Number of Gallstones and Survival 1
Analytical Cellular Pathology
title DNA Ploidy and S-Phase Fraction in Carcinoma of the Gallbladder Related to Histopathology, Number of Gallstones and Survival 1
title_full DNA Ploidy and S-Phase Fraction in Carcinoma of the Gallbladder Related to Histopathology, Number of Gallstones and Survival 1
title_fullStr DNA Ploidy and S-Phase Fraction in Carcinoma of the Gallbladder Related to Histopathology, Number of Gallstones and Survival 1
title_full_unstemmed DNA Ploidy and S-Phase Fraction in Carcinoma of the Gallbladder Related to Histopathology, Number of Gallstones and Survival 1
title_short DNA Ploidy and S-Phase Fraction in Carcinoma of the Gallbladder Related to Histopathology, Number of Gallstones and Survival 1
title_sort dna ploidy and s phase fraction in carcinoma of the gallbladder related to histopathology number of gallstones and survival 1
url http://dx.doi.org/10.1155/2001/469630
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