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Clinicopathological and prognostic correlations of HER3 expression and its degradation regulators, NEDD4-1 and NRDP1, in primary breast cancer.

AbstractBACKGROUND:
Human epidermal growth factor receptor HER3 (ErbB3), especially in association with its relative HER2 (ErbB2), is known as a key oncogene in breast tumour biology. Nonetheless, the prognostic relevance of HER3 remains controversial. NEDD4-1 and NRDP1 are signalling molecules closely related to the degradation of HER3 via ubiquitination. NEDD4-1 and NRDP1 have been reported to contribute to HER3-mediated signalling by regulating its localization and cell membrane retention. We studied correlations between HER3, NEDD4-1, and NRDP1 protein expression and their association with tumour histopathological characteristics and clinical outcomes.
METHODS:
The prevalence of immunohistochemically detectable expression profiles of HER3 (n = 177), NEDD4-1 (n = 145), and NRDP1 (n = 145) proteins was studied in primary breast carcinomas on archival formalin-fixed paraffin-embedded (FFPE) samples. Clinicopathological correlations were determined statistically using Pearson's Chi-Square test. The Kaplan-Meier method, log-rank test (Mantel-Cox), and Cox regression analysis were utilized for survival analysis.
RESULTS:
HER3 protein was expressed in breast carcinomas without association with HER2 gene amplification status. Absence or low HER3 expression correlated with clinically aggressive features, such as triple-negative breast cancer (TNBC) phenotype, basal cell origin (cytokeratin 5/14 expression combined with ER negativity), large tumour size, and positive lymph node status. Low total HER3 expression was prognostic for shorter recurrence-free survival time in HER2-amplified breast cancer (p = 0.004, p = 0.020 in univariate and multivariate analyses, respectively). The majority (82.8%) of breast cancers demonstrated NEDD4-1 protein expression - while only a minor proportion (8.3%) of carcinomas expressed NRDP1. NEDD4-1 and NRDP1 expression were not associated with clinical outcomes in HER2-amplified breast cancer, irrespective of adjuvant trastuzumab therapy.
CONCLUSIONS:
Low HER3 expression is suggested to be a valuable prognostic biomarker to predict recurrence in HER2-amplified breast cancer. Neither NEDD4-1 nor NRDP1 demonstrated relevance in prognostics or in the subclassification of HER2-amplified breast carcinomas.
AuthorsSatu Luhtala, Synnöve Staff, Anne Kallioniemi, Minna Tanner, Jorma Isola
JournalBMC cancer (BMC Cancer) Vol. 18 Issue 1 Pg. 1045 (Oct 26 2018) ISSN: 1471-2407 [Electronic] England
PMID30367623 (Publication Type: Journal Article)
Chemical References
  • Biomarkers
  • Nedd4 Ubiquitin Protein Ligases
  • Nedd4 protein, human
  • RNF41 protein, human
  • Ubiquitin-Protein Ligases
  • ERBB2 protein, human
  • Receptor, ErbB-2
  • Receptor, ErbB-3
Topics
  • Adult
  • Aged
  • Aged, 80 and over
  • Biomarkers
  • Breast Neoplasms (genetics, metabolism, mortality, pathology)
  • Female
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Immunohistochemistry
  • Kaplan-Meier Estimate
  • Middle Aged
  • Nedd4 Ubiquitin Protein Ligases (metabolism)
  • Neoplasm Grading
  • Neoplasm Staging
  • Prognosis
  • Proportional Hazards Models
  • Receptor, ErbB-2 (genetics, metabolism)
  • Receptor, ErbB-3 (genetics, metabolism)
  • Ubiquitin-Protein Ligases (metabolism)

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