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Oestrogen-regulated protein SLC39A6: a biomarker of good prognosis in luminal breast cancer

PURPOSE: The outcome of the luminal oestrogen receptor-positive (ER +) subtype of breast cancer (BC) is highly variable and patient stratification needs to be refined. We assessed the prognostic significance of oestrogen-regulated solute carrier family 39 member 6 (SLC39A6) in BC, with emphasis on E...

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Autores principales: Althobiti, Maryam, El-sharawy, Khloud A., Joseph, Chitra, Aleskandarany, Mohammed, Toss, Michael S., Green, Andrew R., Rakha, Emad A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8505289/
https://www.ncbi.nlm.nih.gov/pubmed/34453638
http://dx.doi.org/10.1007/s10549-021-06336-y
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author Althobiti, Maryam
El-sharawy, Khloud A.
Joseph, Chitra
Aleskandarany, Mohammed
Toss, Michael S.
Green, Andrew R.
Rakha, Emad A.
author_facet Althobiti, Maryam
El-sharawy, Khloud A.
Joseph, Chitra
Aleskandarany, Mohammed
Toss, Michael S.
Green, Andrew R.
Rakha, Emad A.
author_sort Althobiti, Maryam
collection PubMed
description PURPOSE: The outcome of the luminal oestrogen receptor-positive (ER +) subtype of breast cancer (BC) is highly variable and patient stratification needs to be refined. We assessed the prognostic significance of oestrogen-regulated solute carrier family 39 member 6 (SLC39A6) in BC, with emphasis on ER + tumours. MATERIALS AND METHODS: SLC39A6 mRNA expression and copy number alterations were assessed using the METABRIC cohort (n = 1980). SLC39A6 protein expression was evaluated in a large (n = 670) and annotated series of early-stage (I–III) operable BC using tissue microarrays and immunohistochemistry. The associations between SLC39A6 expression and clinicopathological parameters, patient outcomes and other ER-related markers were evaluated using Chi-square tests and Kaplan–Meier curves. RESULTS: High SLC39A6 mRNA and protein expression was associated with features characteristic of less aggressive tumours in the entire BC cohort and ER + subgroup. SLC39A6 protein expression was detected in the cytoplasm and nuclei of the tumour cells. High SLC39A6 nuclear expression and mRNA levels were positively associated with ER + tumours and expression of ER-related markers, including the progesterone receptor, forkhead box protein A1 and GATA binding protein 3. In the ER + luminal BC, high SLC39A6 expression was independently associated with longer BC-specific survival (BCSS) (P = 0.015, HR 0.678, 95% CI 0.472‒0.972) even in those who did not receive endocrine therapy (P = 0.001, HR 0.701, 95% CI 0.463‒1.062). CONCLUSION: SLC39A6 may be prognostic for a better outcome in ER + luminal BC. Further functional studies to investigate the role of SLC39A6 in ER + luminal BC are warranted. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10549-021-06336-y.
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spelling pubmed-85052892021-10-19 Oestrogen-regulated protein SLC39A6: a biomarker of good prognosis in luminal breast cancer Althobiti, Maryam El-sharawy, Khloud A. Joseph, Chitra Aleskandarany, Mohammed Toss, Michael S. Green, Andrew R. Rakha, Emad A. Breast Cancer Res Treat Preclinical Study PURPOSE: The outcome of the luminal oestrogen receptor-positive (ER +) subtype of breast cancer (BC) is highly variable and patient stratification needs to be refined. We assessed the prognostic significance of oestrogen-regulated solute carrier family 39 member 6 (SLC39A6) in BC, with emphasis on ER + tumours. MATERIALS AND METHODS: SLC39A6 mRNA expression and copy number alterations were assessed using the METABRIC cohort (n = 1980). SLC39A6 protein expression was evaluated in a large (n = 670) and annotated series of early-stage (I–III) operable BC using tissue microarrays and immunohistochemistry. The associations between SLC39A6 expression and clinicopathological parameters, patient outcomes and other ER-related markers were evaluated using Chi-square tests and Kaplan–Meier curves. RESULTS: High SLC39A6 mRNA and protein expression was associated with features characteristic of less aggressive tumours in the entire BC cohort and ER + subgroup. SLC39A6 protein expression was detected in the cytoplasm and nuclei of the tumour cells. High SLC39A6 nuclear expression and mRNA levels were positively associated with ER + tumours and expression of ER-related markers, including the progesterone receptor, forkhead box protein A1 and GATA binding protein 3. In the ER + luminal BC, high SLC39A6 expression was independently associated with longer BC-specific survival (BCSS) (P = 0.015, HR 0.678, 95% CI 0.472‒0.972) even in those who did not receive endocrine therapy (P = 0.001, HR 0.701, 95% CI 0.463‒1.062). CONCLUSION: SLC39A6 may be prognostic for a better outcome in ER + luminal BC. Further functional studies to investigate the role of SLC39A6 in ER + luminal BC are warranted. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10549-021-06336-y. Springer US 2021-08-28 2021 /pmc/articles/PMC8505289/ /pubmed/34453638 http://dx.doi.org/10.1007/s10549-021-06336-y Text en © The Author(s) 2021 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/) .
spellingShingle Preclinical Study
Althobiti, Maryam
El-sharawy, Khloud A.
Joseph, Chitra
Aleskandarany, Mohammed
Toss, Michael S.
Green, Andrew R.
Rakha, Emad A.
Oestrogen-regulated protein SLC39A6: a biomarker of good prognosis in luminal breast cancer
title Oestrogen-regulated protein SLC39A6: a biomarker of good prognosis in luminal breast cancer
title_full Oestrogen-regulated protein SLC39A6: a biomarker of good prognosis in luminal breast cancer
title_fullStr Oestrogen-regulated protein SLC39A6: a biomarker of good prognosis in luminal breast cancer
title_full_unstemmed Oestrogen-regulated protein SLC39A6: a biomarker of good prognosis in luminal breast cancer
title_short Oestrogen-regulated protein SLC39A6: a biomarker of good prognosis in luminal breast cancer
title_sort oestrogen-regulated protein slc39a6: a biomarker of good prognosis in luminal breast cancer
topic Preclinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8505289/
https://www.ncbi.nlm.nih.gov/pubmed/34453638
http://dx.doi.org/10.1007/s10549-021-06336-y
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