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YKL-40 protein expression in human tumor samples and human tumor cell line xenografts: implications for its use in tumor models
BACKGROUND: YKL-40, also known as non-enzymatic chitinase-3 like-protein-1 (CHI3L1), is a glycoprotein expressed and secreted mainly by inflammatory cells and tumor cells. Accordingly, several studies demonstrated elevated YKL-40 serum levels in cancer patients and found YKL-40 to be correlated with...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8516773/ https://www.ncbi.nlm.nih.gov/pubmed/34432260 http://dx.doi.org/10.1007/s13402-021-00630-z |
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author | Böckelmann, Lukas Clemens Felix, Theresa Calabrò, Simona Schumacher, Udo |
author_facet | Böckelmann, Lukas Clemens Felix, Theresa Calabrò, Simona Schumacher, Udo |
author_sort | Böckelmann, Lukas Clemens |
collection | PubMed |
description | BACKGROUND: YKL-40, also known as non-enzymatic chitinase-3 like-protein-1 (CHI3L1), is a glycoprotein expressed and secreted mainly by inflammatory cells and tumor cells. Accordingly, several studies demonstrated elevated YKL-40 serum levels in cancer patients and found YKL-40 to be correlated with a poor prognosis and disease severity in some tumor entities. YKL-40 was suggested to be involved in angiogenesis and extracellular matrix remodeling. As yet, however, its precise biological function remains elusive. METHODS: As YKL-40 protein expression has only been investigated in few malignancies, we employed immunohistochemical detection in a large multi-tumor tissue microarray consisting of 2,310 samples from 72 different tumor entities. In addition, YKL-40 protein expression was determined in primary mouse xenograft tumors derived from human cancer cell lines. RESULTS: YKL-40 could be detected in almost all cancer entities and was differently expressed depending on tumor stage and subtype (e.g., thyroid cancer, colorectal cancer, gastric cancer and ovarian cancer). While YKL-40 was absent in in vitro grown human cancer cell lines, YKL-40 expression was upregulated in xenograft tumor tissues in vivo. CONCLUSIONS: These data provide new insights into YKL-40 expression at the protein level in various tumor entities and its regulation in tumor models. Our data suggest that upregulation of YKL-40 expression is a common feature in vivo and is finely regulated by tumor cell-microenvironment interactions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13402-021-00630-z. |
format | Online Article Text |
id | pubmed-8516773 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-85167732021-10-29 YKL-40 protein expression in human tumor samples and human tumor cell line xenografts: implications for its use in tumor models Böckelmann, Lukas Clemens Felix, Theresa Calabrò, Simona Schumacher, Udo Cell Oncol (Dordr) Original Article BACKGROUND: YKL-40, also known as non-enzymatic chitinase-3 like-protein-1 (CHI3L1), is a glycoprotein expressed and secreted mainly by inflammatory cells and tumor cells. Accordingly, several studies demonstrated elevated YKL-40 serum levels in cancer patients and found YKL-40 to be correlated with a poor prognosis and disease severity in some tumor entities. YKL-40 was suggested to be involved in angiogenesis and extracellular matrix remodeling. As yet, however, its precise biological function remains elusive. METHODS: As YKL-40 protein expression has only been investigated in few malignancies, we employed immunohistochemical detection in a large multi-tumor tissue microarray consisting of 2,310 samples from 72 different tumor entities. In addition, YKL-40 protein expression was determined in primary mouse xenograft tumors derived from human cancer cell lines. RESULTS: YKL-40 could be detected in almost all cancer entities and was differently expressed depending on tumor stage and subtype (e.g., thyroid cancer, colorectal cancer, gastric cancer and ovarian cancer). While YKL-40 was absent in in vitro grown human cancer cell lines, YKL-40 expression was upregulated in xenograft tumor tissues in vivo. CONCLUSIONS: These data provide new insights into YKL-40 expression at the protein level in various tumor entities and its regulation in tumor models. Our data suggest that upregulation of YKL-40 expression is a common feature in vivo and is finely regulated by tumor cell-microenvironment interactions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13402-021-00630-z. Springer Netherlands 2021-08-25 2021 /pmc/articles/PMC8516773/ /pubmed/34432260 http://dx.doi.org/10.1007/s13402-021-00630-z Text en © The Author(s) 2021, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Böckelmann, Lukas Clemens Felix, Theresa Calabrò, Simona Schumacher, Udo YKL-40 protein expression in human tumor samples and human tumor cell line xenografts: implications for its use in tumor models |
title | YKL-40 protein expression in human tumor samples and human tumor cell line xenografts: implications for its use in tumor models |
title_full | YKL-40 protein expression in human tumor samples and human tumor cell line xenografts: implications for its use in tumor models |
title_fullStr | YKL-40 protein expression in human tumor samples and human tumor cell line xenografts: implications for its use in tumor models |
title_full_unstemmed | YKL-40 protein expression in human tumor samples and human tumor cell line xenografts: implications for its use in tumor models |
title_short | YKL-40 protein expression in human tumor samples and human tumor cell line xenografts: implications for its use in tumor models |
title_sort | ykl-40 protein expression in human tumor samples and human tumor cell line xenografts: implications for its use in tumor models |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8516773/ https://www.ncbi.nlm.nih.gov/pubmed/34432260 http://dx.doi.org/10.1007/s13402-021-00630-z |
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