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Cervical carcinoma-associated fibroblasts are DNA diploid and do not show evidence for somatic genetic alterations

BACKGROUND: Cancer-associated fibroblasts (CAFs) have been recognized as important contributors to cancer development and progression. However, opposing evidence has been published whether CAFs, in addition to epigenetic, also undergo somatic genetic alterations and whether these changes contribute...

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Autores principales: Corver, Willem Ernst, ter Haar, Natalja Tatjana, Fleuren, Gert Jan, Oosting, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3223353/
https://www.ncbi.nlm.nih.gov/pubmed/22042555
http://dx.doi.org/10.1007/s13402-011-0061-5
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author Corver, Willem Ernst
ter Haar, Natalja Tatjana
Fleuren, Gert Jan
Oosting, Jan
author_facet Corver, Willem Ernst
ter Haar, Natalja Tatjana
Fleuren, Gert Jan
Oosting, Jan
author_sort Corver, Willem Ernst
collection PubMed
description BACKGROUND: Cancer-associated fibroblasts (CAFs) have been recognized as important contributors to cancer development and progression. However, opposing evidence has been published whether CAFs, in addition to epigenetic, also undergo somatic genetic alterations and whether these changes contribute to carcinogenesis and tumour progression. METHODS: We combined multiparameter DNA flow cytometry, flow-sorting and 6K SNP-arrays to study DNA aneuploidy, % S-phase, loss of heterozygosity (LOH) and copy number alterations (CNAs) in cervical cancer-associated stromal cell fractions (n = 57) from formalin-fixed, paraffin-embedded (FFPE) samples. Tissue sections were examined for the presence of CAFs. Microsatellite analysis was used to confirm LOH findings. RESULTS: Smooth muscle actin and vimentin immunohistochemistry verified the presence of CAFs in all cases tested. However, we found no evidence for DNA aneuploidy, somatic genetic alterations in the vimentin-positive stromal cell fractions of any samples, while high frequencies of DNA content abnormalities (43/57) and substantial numbers of CNAs and LOH were identified in the keratin-positive epithelial cell fractions. LOH hot-spots on chromosomes 3p, 4p and 6p found were confirmed by microsatellite analysis. CONCLUSION: From our study we conclude that stromal cell fractions from cervical carcinomas are DNA diploid, have a genotype undistinguishable from patient-matched normal tissue and are genetically stable. Using flow cytometry and SNP-arrays, stromal genetic changes do not seem to play a role during cervical carcinogenesis and progression. In addition, the stromal cell fraction of cervical carcinomas can be used as reference allowing large retrospective studies of archival FFPE tissues for which no normal reference tissue is available. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s13402-011-0061-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-32233532011-12-27 Cervical carcinoma-associated fibroblasts are DNA diploid and do not show evidence for somatic genetic alterations Corver, Willem Ernst ter Haar, Natalja Tatjana Fleuren, Gert Jan Oosting, Jan Cell Oncol (Dordr) Original Paper BACKGROUND: Cancer-associated fibroblasts (CAFs) have been recognized as important contributors to cancer development and progression. However, opposing evidence has been published whether CAFs, in addition to epigenetic, also undergo somatic genetic alterations and whether these changes contribute to carcinogenesis and tumour progression. METHODS: We combined multiparameter DNA flow cytometry, flow-sorting and 6K SNP-arrays to study DNA aneuploidy, % S-phase, loss of heterozygosity (LOH) and copy number alterations (CNAs) in cervical cancer-associated stromal cell fractions (n = 57) from formalin-fixed, paraffin-embedded (FFPE) samples. Tissue sections were examined for the presence of CAFs. Microsatellite analysis was used to confirm LOH findings. RESULTS: Smooth muscle actin and vimentin immunohistochemistry verified the presence of CAFs in all cases tested. However, we found no evidence for DNA aneuploidy, somatic genetic alterations in the vimentin-positive stromal cell fractions of any samples, while high frequencies of DNA content abnormalities (43/57) and substantial numbers of CNAs and LOH were identified in the keratin-positive epithelial cell fractions. LOH hot-spots on chromosomes 3p, 4p and 6p found were confirmed by microsatellite analysis. CONCLUSION: From our study we conclude that stromal cell fractions from cervical carcinomas are DNA diploid, have a genotype undistinguishable from patient-matched normal tissue and are genetically stable. Using flow cytometry and SNP-arrays, stromal genetic changes do not seem to play a role during cervical carcinogenesis and progression. In addition, the stromal cell fraction of cervical carcinomas can be used as reference allowing large retrospective studies of archival FFPE tissues for which no normal reference tissue is available. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s13402-011-0061-5) contains supplementary material, which is available to authorized users. Springer Netherlands 2011-11-01 2011 /pmc/articles/PMC3223353/ /pubmed/22042555 http://dx.doi.org/10.1007/s13402-011-0061-5 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Paper
Corver, Willem Ernst
ter Haar, Natalja Tatjana
Fleuren, Gert Jan
Oosting, Jan
Cervical carcinoma-associated fibroblasts are DNA diploid and do not show evidence for somatic genetic alterations
title Cervical carcinoma-associated fibroblasts are DNA diploid and do not show evidence for somatic genetic alterations
title_full Cervical carcinoma-associated fibroblasts are DNA diploid and do not show evidence for somatic genetic alterations
title_fullStr Cervical carcinoma-associated fibroblasts are DNA diploid and do not show evidence for somatic genetic alterations
title_full_unstemmed Cervical carcinoma-associated fibroblasts are DNA diploid and do not show evidence for somatic genetic alterations
title_short Cervical carcinoma-associated fibroblasts are DNA diploid and do not show evidence for somatic genetic alterations
title_sort cervical carcinoma-associated fibroblasts are dna diploid and do not show evidence for somatic genetic alterations
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3223353/
https://www.ncbi.nlm.nih.gov/pubmed/22042555
http://dx.doi.org/10.1007/s13402-011-0061-5
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