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Involvement of NY-ESO-1 and MAGE-A4 in the pathogenesis of desmoid tumors
The involvement of New York esophageal squamous cell carcinoma-1 (NY-ESO-1) and melanoma-associated antigen A4 (MAGE-A4) in soft-tissue sarcoma pathogenesis has recently been reported; however, their involvement in desmoid tumors (DTs) remains unknown. This study aimed to determine the involvement o...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10238029/ https://www.ncbi.nlm.nih.gov/pubmed/37266606 http://dx.doi.org/10.1097/MD.0000000000033908 |
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author | Hashimoto, Kazuhiko Nishimura, Shunji Shinyashiki, Yu Ito, Tomohiko Kakinoki, Ryosuke Akagi, Masao |
author_facet | Hashimoto, Kazuhiko Nishimura, Shunji Shinyashiki, Yu Ito, Tomohiko Kakinoki, Ryosuke Akagi, Masao |
author_sort | Hashimoto, Kazuhiko |
collection | PubMed |
description | The involvement of New York esophageal squamous cell carcinoma-1 (NY-ESO-1) and melanoma-associated antigen A4 (MAGE-A4) in soft-tissue sarcoma pathogenesis has recently been reported; however, their involvement in desmoid tumors (DTs) remains unknown. This study aimed to determine the involvement of NY-ESO-1 and MAGE-A4 in DTs. Immunostaining for β-catenin, NY-ESO-1, and MAGE-A4 was performed on DT biopsy specimens harvested at our institution. The positivity rate for each immune component was calculated. In addition, the correlations between the positivity rates for the immune molecules were investigated. The correlation between the positivity rate and age or longest diameter of each immune molecule was also investigated. β-catenin showed staining mainly in the tumor cell nuclei of DTs. Both NY-ESO-1 and MAGE-A4 showed staining in the nucleus, cytoplasm, and infiltrating lymphocytes of DT cells. The mean positive cell rates for β-catenin, NY-ESO-1, and MAGE-A4 were 43.9 ± 21.7, 30 ± 21.6, and 68.9 ± 20.8, respectively. A strong negative correlation was observed between β-catenin and MAGE-A4 positivity rates (r = −0.64). The positivity rates for NY-ESO-1 and MAGE-A4 showed a moderate positive correlation (r = −0.42). A very strong negative correlation was observed between age and the NY-ESO-1 positivity rate (r = −0.72). A weak negative correlation was observed between age and the MAGE-A4 positivity rate (r = −0.28). A medium negative correlation was observed between the longest tumor diameter and NY-ESO-1 positivity (r = −0.37). NY-ESO-1 and MAGE-A4 may be involved in the DT microenvironment. Thus, NY-ESO-1 and MAGE-A4 may be useful in the diagnosis of DT. |
format | Online Article Text |
id | pubmed-10238029 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-102380292023-06-03 Involvement of NY-ESO-1 and MAGE-A4 in the pathogenesis of desmoid tumors Hashimoto, Kazuhiko Nishimura, Shunji Shinyashiki, Yu Ito, Tomohiko Kakinoki, Ryosuke Akagi, Masao Medicine (Baltimore) 3600 The involvement of New York esophageal squamous cell carcinoma-1 (NY-ESO-1) and melanoma-associated antigen A4 (MAGE-A4) in soft-tissue sarcoma pathogenesis has recently been reported; however, their involvement in desmoid tumors (DTs) remains unknown. This study aimed to determine the involvement of NY-ESO-1 and MAGE-A4 in DTs. Immunostaining for β-catenin, NY-ESO-1, and MAGE-A4 was performed on DT biopsy specimens harvested at our institution. The positivity rate for each immune component was calculated. In addition, the correlations between the positivity rates for the immune molecules were investigated. The correlation between the positivity rate and age or longest diameter of each immune molecule was also investigated. β-catenin showed staining mainly in the tumor cell nuclei of DTs. Both NY-ESO-1 and MAGE-A4 showed staining in the nucleus, cytoplasm, and infiltrating lymphocytes of DT cells. The mean positive cell rates for β-catenin, NY-ESO-1, and MAGE-A4 were 43.9 ± 21.7, 30 ± 21.6, and 68.9 ± 20.8, respectively. A strong negative correlation was observed between β-catenin and MAGE-A4 positivity rates (r = −0.64). The positivity rates for NY-ESO-1 and MAGE-A4 showed a moderate positive correlation (r = −0.42). A very strong negative correlation was observed between age and the NY-ESO-1 positivity rate (r = −0.72). A weak negative correlation was observed between age and the MAGE-A4 positivity rate (r = −0.28). A medium negative correlation was observed between the longest tumor diameter and NY-ESO-1 positivity (r = −0.37). NY-ESO-1 and MAGE-A4 may be involved in the DT microenvironment. Thus, NY-ESO-1 and MAGE-A4 may be useful in the diagnosis of DT. Lippincott Williams & Wilkins 2023-06-02 /pmc/articles/PMC10238029/ /pubmed/37266606 http://dx.doi.org/10.1097/MD.0000000000033908 Text en Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | 3600 Hashimoto, Kazuhiko Nishimura, Shunji Shinyashiki, Yu Ito, Tomohiko Kakinoki, Ryosuke Akagi, Masao Involvement of NY-ESO-1 and MAGE-A4 in the pathogenesis of desmoid tumors |
title | Involvement of NY-ESO-1 and MAGE-A4 in the pathogenesis of desmoid tumors |
title_full | Involvement of NY-ESO-1 and MAGE-A4 in the pathogenesis of desmoid tumors |
title_fullStr | Involvement of NY-ESO-1 and MAGE-A4 in the pathogenesis of desmoid tumors |
title_full_unstemmed | Involvement of NY-ESO-1 and MAGE-A4 in the pathogenesis of desmoid tumors |
title_short | Involvement of NY-ESO-1 and MAGE-A4 in the pathogenesis of desmoid tumors |
title_sort | involvement of ny-eso-1 and mage-a4 in the pathogenesis of desmoid tumors |
topic | 3600 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10238029/ https://www.ncbi.nlm.nih.gov/pubmed/37266606 http://dx.doi.org/10.1097/MD.0000000000033908 |
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