The predictive potential of Neuronatin for neoadjuvant chemotherapy of breast cancer
- PMID: 34092612
- DOI: 10.3233/CBM-203127
The predictive potential of Neuronatin for neoadjuvant chemotherapy of breast cancer
Abstract
Background: Neuronatin (NNAT) determined by immunohistochemistry is a negative prognostic biomarker for breast cancer, independent of the major clinicopathological markers.
Objective: Here, we investigated whether NNAT is also a predictive biomarker for pathological remission after neoadjuvant chemotherapy.
Methods: One hundred and four breast cancer patients, treated with systemic neoadjuvant chemotherapy were included in this retrospective study. NNAT was detected in formaldehyde fixed, paraffin embedded primary cancer tissue by immunohistochemistry and an immuno-reactive score (IRS) determined. Pathological remission was scored according to Sinn and by evaluation of cytopathic effects. NNAT-IRS was correlated with clinicopathological parameters as well as relapse free and overall survival and for pathological remission after neoadjuvant therapy.
Results: NNAT IRS was an independent prognostic marker for relapse free and overall survival and the time from diagnosis to the "tumor-free" state. NNAT IRS was associated with Luminal-A tumors and correlated slightly negative with age and lymph-node metastasis. There was no significant correlation of NNAT-IRS with Sinn's remission score, but with cytopathic effects of chemotherapy.
Conclusions: We confirmed the prognostic impact of NNAT-IRS in an independent cohort of neoadjuvantly treated patients. Additionally, a correlation with a score for pathological remission under systemic neoadjuvant chemotherapy for breast cancer was found.
Keywords: Breast cancer; neoadjuvant chemotherapy; neuronatin; remission score.
Similar articles
-
Platelet/Lymphocyte Ratio Is Superior to Neutrophil/Lymphocyte Ratio as a Predictor of Chemotherapy Response and Disease-free Survival in Luminal B-like (HER2-) Breast Cancer.Clin Breast Cancer. 2020 Aug;20(4):e403-e409. doi: 10.1016/j.clbc.2020.01.008. Epub 2020 Jan 30. Clin Breast Cancer. 2020. PMID: 32201163
-
High neuronatin (NNAT) expression is associated with poor outcome in breast cancer.Virchows Arch. 2017 Jul;471(1):23-30. doi: 10.1007/s00428-017-2154-7. Epub 2017 May 24. Virchows Arch. 2017. PMID: 28540450
-
Expression of Cyclin D1 protein in residual tumor after neoadjuvant chemotherapy for breast cancer.Breast Cancer Res Treat. 2018 Feb;168(1):179-187. doi: 10.1007/s10549-017-4581-1. Epub 2017 Nov 25. Breast Cancer Res Treat. 2018. PMID: 29177689
-
Can the Neutrophil to Lymphocyte Ratio Predict Complete Pathologic Response to Neoadjuvant Breast Cancer Treatment? A Systematic Review and Meta-analysis.Clin Breast Cancer. 2020 Dec;20(6):e675-e681. doi: 10.1016/j.clbc.2020.05.008. Epub 2020 May 16. Clin Breast Cancer. 2020. PMID: 32653471
-
PD-L1 Acts as a Promising Immune Marker to Predict the Response to Neoadjuvant Chemotherapy in Breast Cancer Patients.Clin Breast Cancer. 2020 Feb;20(1):e99-e111. doi: 10.1016/j.clbc.2019.06.014. Epub 2019 Aug 21. Clin Breast Cancer. 2020. PMID: 31521537
Cited by
-
Exploring tumor-normal cross-talk with TranNet: Role of the environment in tumor progression.PLoS Comput Biol. 2023 Sep 18;19(9):e1011472. doi: 10.1371/journal.pcbi.1011472. eCollection 2023 Sep. PLoS Comput Biol. 2023. PMID: 37721939 Free PMC article.
-
Neuronatin Promotes the Progression of Non-small Cell Lung Cancer by Activating the NF-κB Signaling.Curr Cancer Drug Targets. 2024;24(11):1128-1143. doi: 10.2174/0115680096271746240103063325. Curr Cancer Drug Targets. 2024. PMID: 38299400
-
Exploring tumor-normal cross-talk with TranNet: role of the environment in tumor progression.bioRxiv [Preprint]. 2023 Feb 24:2023.02.24.529899. doi: 10.1101/2023.02.24.529899. bioRxiv. 2023. Update in: PLoS Comput Biol. 2023 Sep 18;19(9):e1011472. doi: 10.1371/journal.pcbi.1011472. PMID: 36945455 Free PMC article. Updated. Preprint.
-
Neuropathiazol induces neuronal-like differentiation in neuroblastoma cells via upregulation of PEG5.Pediatr Res. 2025 Feb 20. doi: 10.1038/s41390-025-03925-1. Online ahead of print. Pediatr Res. 2025. PMID: 39972157
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Molecular Biology Databases