Evaluation of ATOX1 as a potential predictive biomarker for tetrathiomolybdate treatment of breast cancer patients with high risk of recurrence Journal Article


Authors: Blockhuys, S.; Hildesjö, C.; Olsson, H.; Vahdat, L.; Wittung-Stafshede, P.
Article Title: Evaluation of ATOX1 as a potential predictive biomarker for tetrathiomolybdate treatment of breast cancer patients with high risk of recurrence
Abstract: Copper plays a key role in cancer metastasis, which is the most common cause of cancer death. Copper depletion treatment with tetrathiomolybdate (TM) improved disease-free survival in breast cancer patients with high risk of recurrence in a phase II clinical trial. Because the copper metallochaperone ATOX1 was recently reported to drive breast cancer cell migration and breast cancer migration is a critical factor in metastasis, we tested if ATOX1 expression levels in primary tumor tissue could predict the TM treatment outcome of breast cancer patients at high risk of recurrence. We performed ATOX1 immunohistochemical staining of breast tumor material (before TM treatment) of 47 patients enrolled in the phase II TM clinical trial and evaluated ATOX1 expression levels in relation with patient outcome after TM treatment. Our results show that higher ATOX1 levels in the tumor cell cytoplasm correlate with a trend towards better event-free survival after TM treatment for triple-negative breast cancer patients and patients at stage III of disease. In conclusion, ATOX1 may be a potential predictive biomarker for TM treatment of breast cancer patients at high risk of recurrence and should be tested in a larger cohort of patients. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
Keywords: clinical trial; breast cancer; biomarker; tetrathiomolybdate; event-free survival; copper depletion; atox1
Journal Title: Biomedicines
Volume: 9
Issue: 12
ISSN: 2227-9059
Publisher: MDPI  
Date Published: 2021-12-01
Start Page: 1887
Language: English
DOI: 10.3390/biomedicines9121887
PROVIDER: scopus
PMCID: PMC8698757
PUBMED: 34944703
DOI/URL:
Notes: Article -- Export Date: 1 February 2022 -- Source: Scopus
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  1. Linda T Vahdat
    43 Vahdat