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DNA content of human kidney carcinoma cells in relation to histological grading.

Ploidy and cell-cycle stage were determined by flow cytometry (FCM) in 46 human renal carcinomas. Cell populations with aneuploid DNA were detected in 46% of these. In the investigated samples, the fraction of cells with abnormal DNA content varied from 8 to 100%. The proliferative activity was gene...

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Autores principales: Baisch, H., Otto, U., König, K., Klöppel, G., Köllermann, M., Linden, W. A.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1982
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2011044/
https://www.ncbi.nlm.nih.gov/pubmed/7093122
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author Baisch, H.
Otto, U.
König, K.
Klöppel, G.
Köllermann, M.
Linden, W. A.
author_facet Baisch, H.
Otto, U.
König, K.
Klöppel, G.
Köllermann, M.
Linden, W. A.
author_sort Baisch, H.
collection PubMed
description Ploidy and cell-cycle stage were determined by flow cytometry (FCM) in 46 human renal carcinomas. Cell populations with aneuploid DNA were detected in 46% of these. In the investigated samples, the fraction of cells with abnormal DNA content varied from 8 to 100%. The proliferative activity was generally low as indicated by the small fractions of cells in S and (G2 + M) phases. This was confirmed by the labelling indices on autoradiographic slides. The fraction of cells in phases S and (G2 + M) for tumours that were pre-irradiated with 15 or 25 Gy before nephrectomy was only slightly less than in unirradiated tumours. Comparison of the FCM ploidy with the results of histological grading showed that all cases classified as the most malignant grades IV or IIIB (according to the nuclear and to the combined grading system of Syrjänen and Hjelt (1978) were hyperdiploid. On the other hand, 45% of the hyperdiploid and 89% of the diploid tumours were of the low grades I and II. After a follow-up for 6 months to 2 years, 8/17 patients with hyperdiploid and only 1/14 patients with diploid tumours have died or relapsed with multiple metastases. The results indicate that the aneuploidy of tumours, measured by FCM, might provide useful additional information for prognosis.
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spelling pubmed-20110442009-09-10 DNA content of human kidney carcinoma cells in relation to histological grading. Baisch, H. Otto, U. König, K. Klöppel, G. Köllermann, M. Linden, W. A. Br J Cancer Research Article Ploidy and cell-cycle stage were determined by flow cytometry (FCM) in 46 human renal carcinomas. Cell populations with aneuploid DNA were detected in 46% of these. In the investigated samples, the fraction of cells with abnormal DNA content varied from 8 to 100%. The proliferative activity was generally low as indicated by the small fractions of cells in S and (G2 + M) phases. This was confirmed by the labelling indices on autoradiographic slides. The fraction of cells in phases S and (G2 + M) for tumours that were pre-irradiated with 15 or 25 Gy before nephrectomy was only slightly less than in unirradiated tumours. Comparison of the FCM ploidy with the results of histological grading showed that all cases classified as the most malignant grades IV or IIIB (according to the nuclear and to the combined grading system of Syrjänen and Hjelt (1978) were hyperdiploid. On the other hand, 45% of the hyperdiploid and 89% of the diploid tumours were of the low grades I and II. After a follow-up for 6 months to 2 years, 8/17 patients with hyperdiploid and only 1/14 patients with diploid tumours have died or relapsed with multiple metastases. The results indicate that the aneuploidy of tumours, measured by FCM, might provide useful additional information for prognosis. Nature Publishing Group 1982-06 /pmc/articles/PMC2011044/ /pubmed/7093122 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Baisch, H.
Otto, U.
König, K.
Klöppel, G.
Köllermann, M.
Linden, W. A.
DNA content of human kidney carcinoma cells in relation to histological grading.
title DNA content of human kidney carcinoma cells in relation to histological grading.
title_full DNA content of human kidney carcinoma cells in relation to histological grading.
title_fullStr DNA content of human kidney carcinoma cells in relation to histological grading.
title_full_unstemmed DNA content of human kidney carcinoma cells in relation to histological grading.
title_short DNA content of human kidney carcinoma cells in relation to histological grading.
title_sort dna content of human kidney carcinoma cells in relation to histological grading.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2011044/
https://www.ncbi.nlm.nih.gov/pubmed/7093122
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