Journal of Clinical Medicine (Dec 2020)

Clinical Significance of ARID1A and ANXA1 in HER-2 Positive Breast Cancer

  • Rita Silva-Oliveira,
  • Filipa Ferreira Pereira,
  • Sara Petronilho,
  • Ana Teresa Martins,
  • Ana Lameirinhas,
  • Vera Constâncio,
  • Inês Caldas-Ribeiro,
  • Sofia Salta,
  • Paula Lopes,
  • Luís Antunes,
  • Fernando Castro,
  • Susana Palma de Sousa,
  • Rui Henrique,
  • Carmen Jerónimo

DOI
https://doi.org/10.3390/jcm9123911
Journal volume & issue
Vol. 9, no. 12
p. 3911

Abstract

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Background: trastuzumab is considered the standard of care for human epidermal growth factor receptor-2 (HER-2+) breast cancer patients. Regardless of the benefits of its use, many early-stage patients eventually recur, and usually, the disease progresses within a year. Since about half of the HER-2+ patients do not respond to trastuzumab, new biomarkers of prognosis and prediction are warranted to allow a better patient stratification. Annexin A1 (ANXA1) was previously reported to contribute to trastuzumab resistance through AKT activation. An association between adenine thymine-rich interactive domain 1A (ARID1A) loss and ANXA1 upregulation was also previously suggested by others. Methods: in this study, we examined tissue samples from 215 HER-2+ breast cancer patients to investigate the value of ARID1A and ANXA1 protein levels in trastuzumab response prediction and patient outcome. Expression of ARID1A and ANXA1 were assessed by immunohistochemistry. Results: contrary to what was expected, no inverse association was found between ARID1A and ANXA1 expression. HER-2+ (non-luminal) tumours displayed higher ANXA1 expression than luminal B-like (HER-2+) tumours. Concerning trastuzumab resistance, ARID1A and ANXA1 proteins did not demonstrate predictive value as biomarkers. Nevertheless, an association was depicted between ANXA1 expression and breast cancer mortality and relapse. Conclusions: overall, our results suggest that ANXA1 may be a useful prognostic marker in HER-2+ patients. Additionally, its ability to discriminate between HER-2+ (non-luminal) and luminal B-like (HER-2+) patients might assist in patient stratification regarding treatment strategy.

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