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Chemokine expression in patients with ovarian cancer or benign ovarian tumors
INTRODUCTION: Chemokines play a crucial role in tumor growth and progression according to proangiogenic and immunosuppressive action. The aim of this study was to investigate the serum levels of selected chemokines in patients with ovarian cancer or benign ovarian tumors to assess their role in tumo...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9102528/ https://www.ncbi.nlm.nih.gov/pubmed/35591828 http://dx.doi.org/10.5114/aoms/110672 |
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author | Nowak, Marek Janas, Łukasz Soja, Malwina Głowacka, Ewa Szyłło, Krzysztof Misiek, Marcin Klink, Magdalena |
author_facet | Nowak, Marek Janas, Łukasz Soja, Malwina Głowacka, Ewa Szyłło, Krzysztof Misiek, Marcin Klink, Magdalena |
author_sort | Nowak, Marek |
collection | PubMed |
description | INTRODUCTION: Chemokines play a crucial role in tumor growth and progression according to proangiogenic and immunosuppressive action. The aim of this study was to investigate the serum levels of selected chemokines in patients with ovarian cancer or benign ovarian tumors to assess their role in tumorigenesis and their potential use in preoperative diagnosis of an adnexal mass. MATERIAL AND METHODS: The study group consisted of 59 women with ovarian cancer: 17 epithelial ovarian cancer (EOC) patients and 42 women with benign ovarian tumors. We measured in sera obtained preoperatively the level of CA125 and a panel of 5 chemokines – CX3CL1/fractalkine, CXCL1/GRO-α, CXCL12/SDF-1, CCL20/MIP-3α and IL-17F – using the chemiluminescence method with multiplexed bead based immunoassay. RESULTS: CX3CL1 was significantly elevated in sera of advanced ovarian cancer patients compared to women with benign ovarian tumors. The significant elevation of CXCL1 was also observed (both early and advanced stages). A similar pattern was present with the standard ovarian cancer marker CA125. In our patients with endometriotic cysts CA125 levels were significantly higher than in women with other benign tumors, whereas all analyzed chemokines had similar serum titers in patients with endometriotic vs. other benign ovarian cysts. CONCLUSIONS: CX3CL1 and CXCL1 are elevated in sera of EOC patients, which indicates their role in cancer development. Moreover, they might be useful in preoperative differential diagnosis of ovarian tumors, especially as they were not elevated in cases of endometriosis. |
format | Online Article Text |
id | pubmed-9102528 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-91025282022-05-18 Chemokine expression in patients with ovarian cancer or benign ovarian tumors Nowak, Marek Janas, Łukasz Soja, Malwina Głowacka, Ewa Szyłło, Krzysztof Misiek, Marcin Klink, Magdalena Arch Med Sci Clinical Research INTRODUCTION: Chemokines play a crucial role in tumor growth and progression according to proangiogenic and immunosuppressive action. The aim of this study was to investigate the serum levels of selected chemokines in patients with ovarian cancer or benign ovarian tumors to assess their role in tumorigenesis and their potential use in preoperative diagnosis of an adnexal mass. MATERIAL AND METHODS: The study group consisted of 59 women with ovarian cancer: 17 epithelial ovarian cancer (EOC) patients and 42 women with benign ovarian tumors. We measured in sera obtained preoperatively the level of CA125 and a panel of 5 chemokines – CX3CL1/fractalkine, CXCL1/GRO-α, CXCL12/SDF-1, CCL20/MIP-3α and IL-17F – using the chemiluminescence method with multiplexed bead based immunoassay. RESULTS: CX3CL1 was significantly elevated in sera of advanced ovarian cancer patients compared to women with benign ovarian tumors. The significant elevation of CXCL1 was also observed (both early and advanced stages). A similar pattern was present with the standard ovarian cancer marker CA125. In our patients with endometriotic cysts CA125 levels were significantly higher than in women with other benign tumors, whereas all analyzed chemokines had similar serum titers in patients with endometriotic vs. other benign ovarian cysts. CONCLUSIONS: CX3CL1 and CXCL1 are elevated in sera of EOC patients, which indicates their role in cancer development. Moreover, they might be useful in preoperative differential diagnosis of ovarian tumors, especially as they were not elevated in cases of endometriosis. Termedia Publishing House 2021-03-21 /pmc/articles/PMC9102528/ /pubmed/35591828 http://dx.doi.org/10.5114/aoms/110672 Text en Copyright: © 2022 Termedia & Banach https://creativecommons.org/licenses/by-nc-sa/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license. |
spellingShingle | Clinical Research Nowak, Marek Janas, Łukasz Soja, Malwina Głowacka, Ewa Szyłło, Krzysztof Misiek, Marcin Klink, Magdalena Chemokine expression in patients with ovarian cancer or benign ovarian tumors |
title | Chemokine expression in patients with ovarian cancer or benign ovarian tumors |
title_full | Chemokine expression in patients with ovarian cancer or benign ovarian tumors |
title_fullStr | Chemokine expression in patients with ovarian cancer or benign ovarian tumors |
title_full_unstemmed | Chemokine expression in patients with ovarian cancer or benign ovarian tumors |
title_short | Chemokine expression in patients with ovarian cancer or benign ovarian tumors |
title_sort | chemokine expression in patients with ovarian cancer or benign ovarian tumors |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9102528/ https://www.ncbi.nlm.nih.gov/pubmed/35591828 http://dx.doi.org/10.5114/aoms/110672 |
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