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Catecholamines Promote Ovarian Cancer Progression through Secretion of CXC-Chemokines

Considerable evidence has accumulated in the last decade supporting the notion that chronic stress is closely related to the growth, metastasis, and angiogenesis of ovarian cancer. In this study, we analyzed the conditioned media in SKOV3 ovarian cancer cell lines treated with catecholamines to iden...

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Autores principales: Kim, Hyun Jung, Chang, Ha Kyun, Lee, Yul Min, Heo, Kyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10532075/
https://www.ncbi.nlm.nih.gov/pubmed/37762405
http://dx.doi.org/10.3390/ijms241814104
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author Kim, Hyun Jung
Chang, Ha Kyun
Lee, Yul Min
Heo, Kyun
author_facet Kim, Hyun Jung
Chang, Ha Kyun
Lee, Yul Min
Heo, Kyun
author_sort Kim, Hyun Jung
collection PubMed
description Considerable evidence has accumulated in the last decade supporting the notion that chronic stress is closely related to the growth, metastasis, and angiogenesis of ovarian cancer. In this study, we analyzed the conditioned media in SKOV3 ovarian cancer cell lines treated with catecholamines to identify secreted proteins responding to chronic stress. Here, we observed that epinephrine and norepinephrine enhanced the secretion and mRNA expression of CXC-chemokines (CXCL1, 2, 3, and 8). Neutralizing antibodies to CXCL8 and CXCL8 receptor (CXCR2) inhibitors significantly reduced catecholamine-mediated invasion of SKOV3 cells. Finally, we found that the concentration of CXCL1 and CXCL8 in the plasma of ovarian cancer patients increased with stage progression. Taken together, these findings suggest that stress-related catecholamines may influence ovarian cancer progression through the secretion of CXC-chemokines.
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spelling pubmed-105320752023-09-28 Catecholamines Promote Ovarian Cancer Progression through Secretion of CXC-Chemokines Kim, Hyun Jung Chang, Ha Kyun Lee, Yul Min Heo, Kyun Int J Mol Sci Article Considerable evidence has accumulated in the last decade supporting the notion that chronic stress is closely related to the growth, metastasis, and angiogenesis of ovarian cancer. In this study, we analyzed the conditioned media in SKOV3 ovarian cancer cell lines treated with catecholamines to identify secreted proteins responding to chronic stress. Here, we observed that epinephrine and norepinephrine enhanced the secretion and mRNA expression of CXC-chemokines (CXCL1, 2, 3, and 8). Neutralizing antibodies to CXCL8 and CXCL8 receptor (CXCR2) inhibitors significantly reduced catecholamine-mediated invasion of SKOV3 cells. Finally, we found that the concentration of CXCL1 and CXCL8 in the plasma of ovarian cancer patients increased with stage progression. Taken together, these findings suggest that stress-related catecholamines may influence ovarian cancer progression through the secretion of CXC-chemokines. MDPI 2023-09-14 /pmc/articles/PMC10532075/ /pubmed/37762405 http://dx.doi.org/10.3390/ijms241814104 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kim, Hyun Jung
Chang, Ha Kyun
Lee, Yul Min
Heo, Kyun
Catecholamines Promote Ovarian Cancer Progression through Secretion of CXC-Chemokines
title Catecholamines Promote Ovarian Cancer Progression through Secretion of CXC-Chemokines
title_full Catecholamines Promote Ovarian Cancer Progression through Secretion of CXC-Chemokines
title_fullStr Catecholamines Promote Ovarian Cancer Progression through Secretion of CXC-Chemokines
title_full_unstemmed Catecholamines Promote Ovarian Cancer Progression through Secretion of CXC-Chemokines
title_short Catecholamines Promote Ovarian Cancer Progression through Secretion of CXC-Chemokines
title_sort catecholamines promote ovarian cancer progression through secretion of cxc-chemokines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10532075/
https://www.ncbi.nlm.nih.gov/pubmed/37762405
http://dx.doi.org/10.3390/ijms241814104
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