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Chemokine Network and Overall Survival in TP53 Wild-Type and Mutant Ovarian Cancer
Ovarian cancer (OC) has the highest mortality rate among gynecological malignancies. Because chemokine network is involved in OC progression, we evaluated associations between chemokine expression and survival in tumor suppressor protein p53 (TP53) wild-type (TP53WT) and mutant (TP53m) OC datasets....
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Association of Immunologists
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6117514/ https://www.ncbi.nlm.nih.gov/pubmed/30181917 http://dx.doi.org/10.4110/in.2018.18.e29 |
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author | Ignacio, Rosa Mistica C. Lee, Eun-Sook Wilson, Andrew J. Beeghly-Fadiel, Alicia Whalen, Margaret M. Son, Deok-Soo |
author_facet | Ignacio, Rosa Mistica C. Lee, Eun-Sook Wilson, Andrew J. Beeghly-Fadiel, Alicia Whalen, Margaret M. Son, Deok-Soo |
author_sort | Ignacio, Rosa Mistica C. |
collection | PubMed |
description | Ovarian cancer (OC) has the highest mortality rate among gynecological malignancies. Because chemokine network is involved in OC progression, we evaluated associations between chemokine expression and survival in tumor suppressor protein p53 (TP53) wild-type (TP53WT) and mutant (TP53m) OC datasets. TP53 was highly mutated in OC compared to other cancer types. Among OC subtypes, CXCL14 was predominantly expressed in clear cell OC, and CCL15 and CCL20 in mucinous OC. TP53WT endometrioid OC highly expressed CXCL14 compared to TP53m, showing better progression-free survival but no difference in overall survival (OS). TP53m serous OC highly expressed CCL8, CCL20, CXCL10 and CXCL11 compared to TP53WT. CXCL12 and CCL21 were associated with poor OS in TP53WT serous OC. CXCR2 was associated with poor OS in TP53m serous OC, while CXCL9, CCL5, CXCR4, CXCL11, and CXCL13 were associated with better OS. Taken together, specific chemokine signatures may differentially influence OS in TP53WT and TP53m OC. |
format | Online Article Text |
id | pubmed-6117514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Korean Association of Immunologists |
record_format | MEDLINE/PubMed |
spelling | pubmed-61175142018-09-04 Chemokine Network and Overall Survival in TP53 Wild-Type and Mutant Ovarian Cancer Ignacio, Rosa Mistica C. Lee, Eun-Sook Wilson, Andrew J. Beeghly-Fadiel, Alicia Whalen, Margaret M. Son, Deok-Soo Immune Netw Brief Communication Ovarian cancer (OC) has the highest mortality rate among gynecological malignancies. Because chemokine network is involved in OC progression, we evaluated associations between chemokine expression and survival in tumor suppressor protein p53 (TP53) wild-type (TP53WT) and mutant (TP53m) OC datasets. TP53 was highly mutated in OC compared to other cancer types. Among OC subtypes, CXCL14 was predominantly expressed in clear cell OC, and CCL15 and CCL20 in mucinous OC. TP53WT endometrioid OC highly expressed CXCL14 compared to TP53m, showing better progression-free survival but no difference in overall survival (OS). TP53m serous OC highly expressed CCL8, CCL20, CXCL10 and CXCL11 compared to TP53WT. CXCL12 and CCL21 were associated with poor OS in TP53WT serous OC. CXCR2 was associated with poor OS in TP53m serous OC, while CXCL9, CCL5, CXCR4, CXCL11, and CXCL13 were associated with better OS. Taken together, specific chemokine signatures may differentially influence OS in TP53WT and TP53m OC. The Korean Association of Immunologists 2018-08-13 /pmc/articles/PMC6117514/ /pubmed/30181917 http://dx.doi.org/10.4110/in.2018.18.e29 Text en Copyright © 2018. The Korean Association of Immunologists https://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Brief Communication Ignacio, Rosa Mistica C. Lee, Eun-Sook Wilson, Andrew J. Beeghly-Fadiel, Alicia Whalen, Margaret M. Son, Deok-Soo Chemokine Network and Overall Survival in TP53 Wild-Type and Mutant Ovarian Cancer |
title | Chemokine Network and Overall Survival in TP53 Wild-Type and Mutant Ovarian Cancer |
title_full | Chemokine Network and Overall Survival in TP53 Wild-Type and Mutant Ovarian Cancer |
title_fullStr | Chemokine Network and Overall Survival in TP53 Wild-Type and Mutant Ovarian Cancer |
title_full_unstemmed | Chemokine Network and Overall Survival in TP53 Wild-Type and Mutant Ovarian Cancer |
title_short | Chemokine Network and Overall Survival in TP53 Wild-Type and Mutant Ovarian Cancer |
title_sort | chemokine network and overall survival in tp53 wild-type and mutant ovarian cancer |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6117514/ https://www.ncbi.nlm.nih.gov/pubmed/30181917 http://dx.doi.org/10.4110/in.2018.18.e29 |
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