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Association of androgen receptor expression with glucose metabolic features in triple-negative breast cancer
BACKGROUND: Androgen receptor (AR) is a potential therapeutic target in triple-negative breast cancer (TNBC). We aimed to elucidate the association of AR expression with glucose metabolic features in TNBC. METHODS: Two independent datasets were analyzed: FDG PET data of our institution and a public...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9524647/ https://www.ncbi.nlm.nih.gov/pubmed/36178912 http://dx.doi.org/10.1371/journal.pone.0275279 |
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author | Lee, Reeree Lee, Han-Byoel Paeng, Jin Chul Choi, Hongyoon Whi, Wonseok Han, Wonshik Seok, Ju Won Kang, Keon Wook Cheon, Gi Jeong |
author_facet | Lee, Reeree Lee, Han-Byoel Paeng, Jin Chul Choi, Hongyoon Whi, Wonseok Han, Wonshik Seok, Ju Won Kang, Keon Wook Cheon, Gi Jeong |
author_sort | Lee, Reeree |
collection | PubMed |
description | BACKGROUND: Androgen receptor (AR) is a potential therapeutic target in triple-negative breast cancer (TNBC). We aimed to elucidate the association of AR expression with glucose metabolic features in TNBC. METHODS: Two independent datasets were analyzed: FDG PET data of our institution and a public dataset of GSE135565. In PET analysis, patients with TNBC who underwent pretreatment PET between Jan 2013 and Dec 2017 were retrospectively enrolled. Clinicopathologic features and maximum standardized uptake value (SUV(max)) of tumors were compared with AR expression. In GSE135565 dataset, glycolysis score was calculated by the pattern of glycolysis-related genes, and of which association with SUV(max) and AR gene expression were analyzed. RESULTS: A total of 608 female patients were included in the PET data of our institution. SUV(max) was lower in AR-positive tumors (P < 0.001) and correlated with lower AR expression (rho = –0.26, P < 0.001). In multivariate analysis, AR was a deterministic factor for low SUV(max) (P = 0.012), along with other key clinicopathologic features. In the GSE135565 dataset, AR expression also exhibited a negative correlation with SUV(max) (r = –0.34, P = 0.001) and the glycolysis score (r = –0.27, P = 0.013). CONCLUSIONS: Low glucose metabolism is a signature of AR expression in TNBC. It is suggested that evaluation of AR expression status needs to be considered in clinical practice particularly in TNBC with low glucose metabolism. |
format | Online Article Text |
id | pubmed-9524647 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-95246472022-10-01 Association of androgen receptor expression with glucose metabolic features in triple-negative breast cancer Lee, Reeree Lee, Han-Byoel Paeng, Jin Chul Choi, Hongyoon Whi, Wonseok Han, Wonshik Seok, Ju Won Kang, Keon Wook Cheon, Gi Jeong PLoS One Research Article BACKGROUND: Androgen receptor (AR) is a potential therapeutic target in triple-negative breast cancer (TNBC). We aimed to elucidate the association of AR expression with glucose metabolic features in TNBC. METHODS: Two independent datasets were analyzed: FDG PET data of our institution and a public dataset of GSE135565. In PET analysis, patients with TNBC who underwent pretreatment PET between Jan 2013 and Dec 2017 were retrospectively enrolled. Clinicopathologic features and maximum standardized uptake value (SUV(max)) of tumors were compared with AR expression. In GSE135565 dataset, glycolysis score was calculated by the pattern of glycolysis-related genes, and of which association with SUV(max) and AR gene expression were analyzed. RESULTS: A total of 608 female patients were included in the PET data of our institution. SUV(max) was lower in AR-positive tumors (P < 0.001) and correlated with lower AR expression (rho = –0.26, P < 0.001). In multivariate analysis, AR was a deterministic factor for low SUV(max) (P = 0.012), along with other key clinicopathologic features. In the GSE135565 dataset, AR expression also exhibited a negative correlation with SUV(max) (r = –0.34, P = 0.001) and the glycolysis score (r = –0.27, P = 0.013). CONCLUSIONS: Low glucose metabolism is a signature of AR expression in TNBC. It is suggested that evaluation of AR expression status needs to be considered in clinical practice particularly in TNBC with low glucose metabolism. Public Library of Science 2022-09-30 /pmc/articles/PMC9524647/ /pubmed/36178912 http://dx.doi.org/10.1371/journal.pone.0275279 Text en © 2022 Lee et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Lee, Reeree Lee, Han-Byoel Paeng, Jin Chul Choi, Hongyoon Whi, Wonseok Han, Wonshik Seok, Ju Won Kang, Keon Wook Cheon, Gi Jeong Association of androgen receptor expression with glucose metabolic features in triple-negative breast cancer |
title | Association of androgen receptor expression with glucose metabolic features in triple-negative breast cancer |
title_full | Association of androgen receptor expression with glucose metabolic features in triple-negative breast cancer |
title_fullStr | Association of androgen receptor expression with glucose metabolic features in triple-negative breast cancer |
title_full_unstemmed | Association of androgen receptor expression with glucose metabolic features in triple-negative breast cancer |
title_short | Association of androgen receptor expression with glucose metabolic features in triple-negative breast cancer |
title_sort | association of androgen receptor expression with glucose metabolic features in triple-negative breast cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9524647/ https://www.ncbi.nlm.nih.gov/pubmed/36178912 http://dx.doi.org/10.1371/journal.pone.0275279 |
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