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High‐grade tumours promote growth of other less‐malignant tumours in the same prostate
Prostate cancer is a multifocal disease, but if and how individual prostate tumours influence each other is largely unknown. We therefore explored signs of direct or indirect tumour–tumour interactions in experimental models and patient samples. Low‐metastatic AT1 and high‐metastatic MatLyLu (MLL) D...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986692/ https://www.ncbi.nlm.nih.gov/pubmed/33330991 http://dx.doi.org/10.1002/path.5604 |
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author | Halin Bergström, Sofia Rudolfsson, Stina Lundholm, Marie Josefsson, Andreas Wikström, Pernilla Bergh, Anders |
author_facet | Halin Bergström, Sofia Rudolfsson, Stina Lundholm, Marie Josefsson, Andreas Wikström, Pernilla Bergh, Anders |
author_sort | Halin Bergström, Sofia |
collection | PubMed |
description | Prostate cancer is a multifocal disease, but if and how individual prostate tumours influence each other is largely unknown. We therefore explored signs of direct or indirect tumour–tumour interactions in experimental models and patient samples. Low‐metastatic AT1 and high‐metastatic MatLyLu (MLL) Dunning rat prostate cancer cells were injected into separate lobes of the ventral prostate of immunocompetent rats. AT1 tumours growing in the same prostate as MLL tumours had increased tumour size and proliferation compared to AT1 tumours growing alone. In addition, the vasculature and macrophage density surrounding the AT1 tumours were increased by MLL tumour closeness. In patient prostatectomy samples, selected to contain an index tumour [tumour with the highest grade, International Society of Urological Pathology (ISUP) grade 1, 2, 3 or 4] and a low‐grade satellite tumour (ISUP grade 1), cell proliferation in low‐grade satellite tumours gradually increased with increasing histological grade of the index tumour. The density of blood vessels and CD68(+) macrophages also increased around the low‐grade satellite tumour if a high‐grade index tumour was present. This suggests that high‐grade tumours, by changing the prostate microenvironment, may increase the aggressiveness of low‐grade lesions in the organ. Future studies are needed to explore the mechanisms behind tumour–tumour interactions and their clinical importance. © 2020 The Authors. The Journal of Pathology published by John Wiley & Sons, Ltd. on behalf of The Pathological Society of Great Britain and Ireland. |
format | Online Article Text |
id | pubmed-7986692 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-79866922021-03-25 High‐grade tumours promote growth of other less‐malignant tumours in the same prostate Halin Bergström, Sofia Rudolfsson, Stina Lundholm, Marie Josefsson, Andreas Wikström, Pernilla Bergh, Anders J Pathol Original Papers Prostate cancer is a multifocal disease, but if and how individual prostate tumours influence each other is largely unknown. We therefore explored signs of direct or indirect tumour–tumour interactions in experimental models and patient samples. Low‐metastatic AT1 and high‐metastatic MatLyLu (MLL) Dunning rat prostate cancer cells were injected into separate lobes of the ventral prostate of immunocompetent rats. AT1 tumours growing in the same prostate as MLL tumours had increased tumour size and proliferation compared to AT1 tumours growing alone. In addition, the vasculature and macrophage density surrounding the AT1 tumours were increased by MLL tumour closeness. In patient prostatectomy samples, selected to contain an index tumour [tumour with the highest grade, International Society of Urological Pathology (ISUP) grade 1, 2, 3 or 4] and a low‐grade satellite tumour (ISUP grade 1), cell proliferation in low‐grade satellite tumours gradually increased with increasing histological grade of the index tumour. The density of blood vessels and CD68(+) macrophages also increased around the low‐grade satellite tumour if a high‐grade index tumour was present. This suggests that high‐grade tumours, by changing the prostate microenvironment, may increase the aggressiveness of low‐grade lesions in the organ. Future studies are needed to explore the mechanisms behind tumour–tumour interactions and their clinical importance. © 2020 The Authors. The Journal of Pathology published by John Wiley & Sons, Ltd. on behalf of The Pathological Society of Great Britain and Ireland. John Wiley & Sons, Ltd 2021-01-26 2021-04 /pmc/articles/PMC7986692/ /pubmed/33330991 http://dx.doi.org/10.1002/path.5604 Text en © 2020 The Authors. The Journal of Pathology published by John Wiley & Sons, Ltd. on behalf of The Pathological Society of Great Britain and Ireland. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Papers Halin Bergström, Sofia Rudolfsson, Stina Lundholm, Marie Josefsson, Andreas Wikström, Pernilla Bergh, Anders High‐grade tumours promote growth of other less‐malignant tumours in the same prostate |
title | High‐grade tumours promote growth of other less‐malignant tumours in the same prostate |
title_full | High‐grade tumours promote growth of other less‐malignant tumours in the same prostate |
title_fullStr | High‐grade tumours promote growth of other less‐malignant tumours in the same prostate |
title_full_unstemmed | High‐grade tumours promote growth of other less‐malignant tumours in the same prostate |
title_short | High‐grade tumours promote growth of other less‐malignant tumours in the same prostate |
title_sort | high‐grade tumours promote growth of other less‐malignant tumours in the same prostate |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986692/ https://www.ncbi.nlm.nih.gov/pubmed/33330991 http://dx.doi.org/10.1002/path.5604 |
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