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Matrix Gla protein (MGP), GATA3, and TRPS1: a novel diagnostic panel to determine breast origin
BACKGROUND: Metastatic breast carcinoma is commonly considered during differential diagnosis when metastatic disease is detected in females. In addition to the tumor morphology and documented clinical history, sensitive and specific immunohistochemical (IHC) markers such as GCDFP-15, mammaglobin, an...
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/PMC9598034/ https://www.ncbi.nlm.nih.gov/pubmed/36284362 http://dx.doi.org/10.1186/s13058-022-01569-1 |
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author | Du, Tian Pan, Lu Zheng, Chengyou Chen, Keming Yang, Yuanzhong Chen, Jiewei Chao, Xue Li, Mei Lu, Jiabin Luo, Rongzhen Zhang, Jinhui Wu, Yu He, Jiehua Jiang, Dongping Sun, Peng |
author_facet | Du, Tian Pan, Lu Zheng, Chengyou Chen, Keming Yang, Yuanzhong Chen, Jiewei Chao, Xue Li, Mei Lu, Jiabin Luo, Rongzhen Zhang, Jinhui Wu, Yu He, Jiehua Jiang, Dongping Sun, Peng |
author_sort | Du, Tian |
collection | PubMed |
description | BACKGROUND: Metastatic breast carcinoma is commonly considered during differential diagnosis when metastatic disease is detected in females. In addition to the tumor morphology and documented clinical history, sensitive and specific immunohistochemical (IHC) markers such as GCDFP-15, mammaglobin, and GATA3 are helpful for determining breast origin. However, these markers are reported to show lower sensitivity in certain subtypes, such as triple-negative breast cancer (TNBC). MATERIALS AND METHODS: Using bioinformatics analyses, we identified a potential diagnostic panel to determine breast origin: matrix Gla protein (MGP), transcriptional repressor GATA binding 1 (TRPS1), and GATA-binding protein 3 (GATA3). We compared MGP, TRPS1, and GATA3 expression in different subtypes of breast carcinoma of (n = 1201) using IHC. As a newly identified marker, MGP expression was also evaluated in solid tumors (n = 2384) and normal tissues (n = 1351) from different organs. RESULTS: MGP and TRPS1 had comparable positive expression in HER2-positive (91.2% vs. 92.0%, p = 0.79) and TNBC subtypes (87.3% vs. 91.2%, p = 0.18). GATA3 expression was lower than MGP (p < 0.001) or TRPS1 (p < 0.001), especially in HER2-positive (77.0%, p < 0.001) and TNBC (43.3%, p < 0.001) subtypes. TRPS1 had the highest positivity rate (97.9%) in metaplastic TNBCs, followed by MGP (88.6%), while only 47.1% of metaplastic TNBCs were positive for GATA3. When using MGP, GATA3, and TRPS1 as a novel IHC panel, 93.0% of breast carcinomas were positive for at least two markers, and only 9 cases were negative for all three markers. MGP was detected in 36 cases (3.0%) that were negative for both GATA3 and TRPS1. MGP showed mild-to-moderate positive expression in normal hepatocytes, renal tubules, as well as 31.1% (99/318) of hepatocellular carcinomas. Rare cases (0.6–5%) had focal MGP expression in renal, ovarian, lung, urothelial, and cholangiocarcinomas. CONCLUSIONS: Our findings suggest that MGP is a newly identified sensitive IHC marker to support breast origin. MGP, TRPS1, and GATA3 could be applied as a reliable diagnostic panel to determine breast origin in clinical practice. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13058-022-01569-1. |
format | Online Article Text |
id | pubmed-9598034 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-95980342022-10-27 Matrix Gla protein (MGP), GATA3, and TRPS1: a novel diagnostic panel to determine breast origin Du, Tian Pan, Lu Zheng, Chengyou Chen, Keming Yang, Yuanzhong Chen, Jiewei Chao, Xue Li, Mei Lu, Jiabin Luo, Rongzhen Zhang, Jinhui Wu, Yu He, Jiehua Jiang, Dongping Sun, Peng Breast Cancer Res Research BACKGROUND: Metastatic breast carcinoma is commonly considered during differential diagnosis when metastatic disease is detected in females. In addition to the tumor morphology and documented clinical history, sensitive and specific immunohistochemical (IHC) markers such as GCDFP-15, mammaglobin, and GATA3 are helpful for determining breast origin. However, these markers are reported to show lower sensitivity in certain subtypes, such as triple-negative breast cancer (TNBC). MATERIALS AND METHODS: Using bioinformatics analyses, we identified a potential diagnostic panel to determine breast origin: matrix Gla protein (MGP), transcriptional repressor GATA binding 1 (TRPS1), and GATA-binding protein 3 (GATA3). We compared MGP, TRPS1, and GATA3 expression in different subtypes of breast carcinoma of (n = 1201) using IHC. As a newly identified marker, MGP expression was also evaluated in solid tumors (n = 2384) and normal tissues (n = 1351) from different organs. RESULTS: MGP and TRPS1 had comparable positive expression in HER2-positive (91.2% vs. 92.0%, p = 0.79) and TNBC subtypes (87.3% vs. 91.2%, p = 0.18). GATA3 expression was lower than MGP (p < 0.001) or TRPS1 (p < 0.001), especially in HER2-positive (77.0%, p < 0.001) and TNBC (43.3%, p < 0.001) subtypes. TRPS1 had the highest positivity rate (97.9%) in metaplastic TNBCs, followed by MGP (88.6%), while only 47.1% of metaplastic TNBCs were positive for GATA3. When using MGP, GATA3, and TRPS1 as a novel IHC panel, 93.0% of breast carcinomas were positive for at least two markers, and only 9 cases were negative for all three markers. MGP was detected in 36 cases (3.0%) that were negative for both GATA3 and TRPS1. MGP showed mild-to-moderate positive expression in normal hepatocytes, renal tubules, as well as 31.1% (99/318) of hepatocellular carcinomas. Rare cases (0.6–5%) had focal MGP expression in renal, ovarian, lung, urothelial, and cholangiocarcinomas. CONCLUSIONS: Our findings suggest that MGP is a newly identified sensitive IHC marker to support breast origin. MGP, TRPS1, and GATA3 could be applied as a reliable diagnostic panel to determine breast origin in clinical practice. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13058-022-01569-1. BioMed Central 2022-10-25 2022 /pmc/articles/PMC9598034/ /pubmed/36284362 http://dx.doi.org/10.1186/s13058-022-01569-1 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 Du, Tian Pan, Lu Zheng, Chengyou Chen, Keming Yang, Yuanzhong Chen, Jiewei Chao, Xue Li, Mei Lu, Jiabin Luo, Rongzhen Zhang, Jinhui Wu, Yu He, Jiehua Jiang, Dongping Sun, Peng Matrix Gla protein (MGP), GATA3, and TRPS1: a novel diagnostic panel to determine breast origin |
title | Matrix Gla protein (MGP), GATA3, and TRPS1: a novel diagnostic panel to determine breast origin |
title_full | Matrix Gla protein (MGP), GATA3, and TRPS1: a novel diagnostic panel to determine breast origin |
title_fullStr | Matrix Gla protein (MGP), GATA3, and TRPS1: a novel diagnostic panel to determine breast origin |
title_full_unstemmed | Matrix Gla protein (MGP), GATA3, and TRPS1: a novel diagnostic panel to determine breast origin |
title_short | Matrix Gla protein (MGP), GATA3, and TRPS1: a novel diagnostic panel to determine breast origin |
title_sort | matrix gla protein (mgp), gata3, and trps1: a novel diagnostic panel to determine breast origin |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9598034/ https://www.ncbi.nlm.nih.gov/pubmed/36284362 http://dx.doi.org/10.1186/s13058-022-01569-1 |
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