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Retinoic acid promotes differentiation of WiT49‐ but not of CCG99‐11 Wilms tumour cells

BACKGROUND: Most children with Wilms tumour are successfully treated with multidrug chemotherapy and surgery. These treatments cause severe side effects for the patients, an issue that needs to be addressed by exploring other treatment options with less or no side effects. One option is to complemen...

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Autores principales: Jansson, Caroline, Mengelbier, Linda Holmquist
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10242656/
https://www.ncbi.nlm.nih.gov/pubmed/37186071
http://dx.doi.org/10.1002/cnr2.1819
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author Jansson, Caroline
Mengelbier, Linda Holmquist
author_facet Jansson, Caroline
Mengelbier, Linda Holmquist
author_sort Jansson, Caroline
collection PubMed
description BACKGROUND: Most children with Wilms tumour are successfully treated with multidrug chemotherapy and surgery. These treatments cause severe side effects for the patients, an issue that needs to be addressed by exploring other treatment options with less or no side effects. One option is to complement current therapies with agents that could potentially induce tumour cell differentiation, for example retinoic acid (RA). AIMS: To facilitate quick assessment of an agent's effect on Wilms tumour differentiation by a rapid in vitro model system. METHODS AND RESULTS: Here WiT49 and CCG99‐11 Wilms tumour cells were treated with 10 μM RA for 72 h or 9 days. Cultured cells were scraped off from Petri dishes, pelleted and embedded in paraffin in the same way as clinical tumour specimens are preserved. Cell morphology and differentiation were evaluated by analyses of haematoxylin eosin (H&E) and immunohistochemical stainings. Based on H&E, WT1 and CKAE1/3 stainings, RA treatment induced further epithelial differentiation of WiT49 cells, whereas there was no sign of induced maturation in CCG99‐11 cells. Ki67 staining showed that RA inhibited cell proliferation in both cell lines. CONCLUSIONS: Our study shows that in vitro culturing of WiT49 and CCG99‐11 cells, followed by pelleting and paraffin embedding of cell pellets, could aid in a quick evaluation of potential differentiating agents against Wilms tumour. In addition, our results strengthen previous results that retinoic acid could be a potential complement to regular Wilms tumour treatment.
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spelling pubmed-102426562023-06-07 Retinoic acid promotes differentiation of WiT49‐ but not of CCG99‐11 Wilms tumour cells Jansson, Caroline Mengelbier, Linda Holmquist Cancer Rep (Hoboken) Original Articles BACKGROUND: Most children with Wilms tumour are successfully treated with multidrug chemotherapy and surgery. These treatments cause severe side effects for the patients, an issue that needs to be addressed by exploring other treatment options with less or no side effects. One option is to complement current therapies with agents that could potentially induce tumour cell differentiation, for example retinoic acid (RA). AIMS: To facilitate quick assessment of an agent's effect on Wilms tumour differentiation by a rapid in vitro model system. METHODS AND RESULTS: Here WiT49 and CCG99‐11 Wilms tumour cells were treated with 10 μM RA for 72 h or 9 days. Cultured cells were scraped off from Petri dishes, pelleted and embedded in paraffin in the same way as clinical tumour specimens are preserved. Cell morphology and differentiation were evaluated by analyses of haematoxylin eosin (H&E) and immunohistochemical stainings. Based on H&E, WT1 and CKAE1/3 stainings, RA treatment induced further epithelial differentiation of WiT49 cells, whereas there was no sign of induced maturation in CCG99‐11 cells. Ki67 staining showed that RA inhibited cell proliferation in both cell lines. CONCLUSIONS: Our study shows that in vitro culturing of WiT49 and CCG99‐11 cells, followed by pelleting and paraffin embedding of cell pellets, could aid in a quick evaluation of potential differentiating agents against Wilms tumour. In addition, our results strengthen previous results that retinoic acid could be a potential complement to regular Wilms tumour treatment. John Wiley and Sons Inc. 2023-04-25 /pmc/articles/PMC10242656/ /pubmed/37186071 http://dx.doi.org/10.1002/cnr2.1819 Text en © 2023 The Authors. Cancer Reports published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://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 Articles
Jansson, Caroline
Mengelbier, Linda Holmquist
Retinoic acid promotes differentiation of WiT49‐ but not of CCG99‐11 Wilms tumour cells
title Retinoic acid promotes differentiation of WiT49‐ but not of CCG99‐11 Wilms tumour cells
title_full Retinoic acid promotes differentiation of WiT49‐ but not of CCG99‐11 Wilms tumour cells
title_fullStr Retinoic acid promotes differentiation of WiT49‐ but not of CCG99‐11 Wilms tumour cells
title_full_unstemmed Retinoic acid promotes differentiation of WiT49‐ but not of CCG99‐11 Wilms tumour cells
title_short Retinoic acid promotes differentiation of WiT49‐ but not of CCG99‐11 Wilms tumour cells
title_sort retinoic acid promotes differentiation of wit49‐ but not of ccg99‐11 wilms tumour cells
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10242656/
https://www.ncbi.nlm.nih.gov/pubmed/37186071
http://dx.doi.org/10.1002/cnr2.1819
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