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Trophoblast cell-surface antigen 2 (TROP2) expression in triple-negative breast cancer
BACKGROUND: Trophoblast cell-surface antigen 2 (TROP2) is related to tumor proliferation enhancement and poor prognosis. An antibody targeting TROP2 was developed to treat metastatic triple-negative breast cancer (TNBC) which has a limited treatment modality. To characterize the TROP2 expressing tum...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9509625/ https://www.ncbi.nlm.nih.gov/pubmed/36153494 http://dx.doi.org/10.1186/s12885-022-10076-7 |
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author | Jeon, Yeonjin Jo, Uiree Hong, Jongmoo Gong, Gyungyub Lee, Hee Jin |
author_facet | Jeon, Yeonjin Jo, Uiree Hong, Jongmoo Gong, Gyungyub Lee, Hee Jin |
author_sort | Jeon, Yeonjin |
collection | PubMed |
description | BACKGROUND: Trophoblast cell-surface antigen 2 (TROP2) is related to tumor proliferation enhancement and poor prognosis. An antibody targeting TROP2 was developed to treat metastatic triple-negative breast cancer (TNBC) which has a limited treatment modality. To characterize the TROP2 expressing tumors in TNBC, we analyzed TROP2 expression in three cohorts; (1) primary tumor without neoadjuvant chemotherapy, (2) primary tumor with neoadjuvant chemotherapy, and (3) metastatic tumor. METHODS: A total of 807 TNBC cases were evaluated for TROP2 immunohistochemical expression. We evaluated the TROP2 H-score distribution in the three cohorts. Tumors were divided into two groups based on TROP2 expression (high vs. low). We analyzed the relationship between clinicopathologic features and markers, including epidermal growth factor receptor, cytokeratin 5/6, p53, and Ki-67, and prognostic significance at high vs. low TROP2 expression. RESULTS: There was no difference in TROP2 H-score distribution between the three cohorts. Moderate-to-strong membranous expression of TROP2 in at least 10% of tumor cells was present in 662 cases (82.0%) in Cohort 1, 59 cases (89.4%) in Cohort 2, and 23 cases (88.5%) in Cohort 3. There was no significant difference in clinicopathologic features between high vs. low TROP2 in all cohorts. TROP2 H-score was an independent poor prognostic factor for overall survival in Cohort 3. CONCLUSIONS: TNBC showed similar TROP2 expression regardless of neoadjuvant treatment or primary tumor/metastasis. Although the prognostic significance of TROP2 expression in metastatic TNBC has been revealed, further evaluation of the predictive value of TROP2 expression for targeted therapy is needed. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-10076-7. |
format | Online Article Text |
id | pubmed-9509625 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-95096252022-09-26 Trophoblast cell-surface antigen 2 (TROP2) expression in triple-negative breast cancer Jeon, Yeonjin Jo, Uiree Hong, Jongmoo Gong, Gyungyub Lee, Hee Jin BMC Cancer Research Article BACKGROUND: Trophoblast cell-surface antigen 2 (TROP2) is related to tumor proliferation enhancement and poor prognosis. An antibody targeting TROP2 was developed to treat metastatic triple-negative breast cancer (TNBC) which has a limited treatment modality. To characterize the TROP2 expressing tumors in TNBC, we analyzed TROP2 expression in three cohorts; (1) primary tumor without neoadjuvant chemotherapy, (2) primary tumor with neoadjuvant chemotherapy, and (3) metastatic tumor. METHODS: A total of 807 TNBC cases were evaluated for TROP2 immunohistochemical expression. We evaluated the TROP2 H-score distribution in the three cohorts. Tumors were divided into two groups based on TROP2 expression (high vs. low). We analyzed the relationship between clinicopathologic features and markers, including epidermal growth factor receptor, cytokeratin 5/6, p53, and Ki-67, and prognostic significance at high vs. low TROP2 expression. RESULTS: There was no difference in TROP2 H-score distribution between the three cohorts. Moderate-to-strong membranous expression of TROP2 in at least 10% of tumor cells was present in 662 cases (82.0%) in Cohort 1, 59 cases (89.4%) in Cohort 2, and 23 cases (88.5%) in Cohort 3. There was no significant difference in clinicopathologic features between high vs. low TROP2 in all cohorts. TROP2 H-score was an independent poor prognostic factor for overall survival in Cohort 3. CONCLUSIONS: TNBC showed similar TROP2 expression regardless of neoadjuvant treatment or primary tumor/metastasis. Although the prognostic significance of TROP2 expression in metastatic TNBC has been revealed, further evaluation of the predictive value of TROP2 expression for targeted therapy is needed. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-10076-7. BioMed Central 2022-09-24 /pmc/articles/PMC9509625/ /pubmed/36153494 http://dx.doi.org/10.1186/s12885-022-10076-7 Text en © The Author(s) 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Jeon, Yeonjin Jo, Uiree Hong, Jongmoo Gong, Gyungyub Lee, Hee Jin Trophoblast cell-surface antigen 2 (TROP2) expression in triple-negative breast cancer |
title | Trophoblast cell-surface antigen 2 (TROP2) expression in triple-negative breast cancer |
title_full | Trophoblast cell-surface antigen 2 (TROP2) expression in triple-negative breast cancer |
title_fullStr | Trophoblast cell-surface antigen 2 (TROP2) expression in triple-negative breast cancer |
title_full_unstemmed | Trophoblast cell-surface antigen 2 (TROP2) expression in triple-negative breast cancer |
title_short | Trophoblast cell-surface antigen 2 (TROP2) expression in triple-negative breast cancer |
title_sort | trophoblast cell-surface antigen 2 (trop2) expression in triple-negative breast cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9509625/ https://www.ncbi.nlm.nih.gov/pubmed/36153494 http://dx.doi.org/10.1186/s12885-022-10076-7 |
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