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Optimization of a Multiplex RNA-based Expression Assay Using Breast Cancer Archival Material
Published on: August 1, 2018
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Nucleostemin expression in invasive breast cancer
Takayuki Kobayashi, Kenkichi Masutomi, Kenji Tamura
1Department of Basic Pathology, National Defense Medical College, 3-2 Namiki, Tokorozawa, Saitama 359-8513, Japan. htsuda@ndmc.ac.jp.
BMC Cancer
|March 22, 2014
Summary
Nucleostemin (NS) is linked to poorer breast cancer prognosis, especially when combined with p53 alterations. NS status may serve as a prognostic marker for luminal and HER2-type breast cancers.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Stem Cell Research
Background:
- The cancer stem cell hypothesis suggests stem-like properties in cancer cells, including self-renewal and differentiation.
- Nucleostemin (NS), a protein found in neural stem cells, is implicated in stemness and nuclear protein binding, including p53.
- NS expression in various cancers highlights its potential role in cancer pathogenesis.
Purpose of the Study:
- To investigate the clinicopathological significance of Nucleostemin (NS) in invasive breast cancers.
- To determine the prognostic impact of NS expression in relation to patient outcomes.
Main Methods:
- Examined NS immunoreactivity in 220 invasive breast cancer tissue samples using tissue microarrays.
- Assessed correlations between nuclear NS and p53 expression (defined as ≥10% positive cells) and clinicopathological parameters.
Main Results:
- NS positivity was observed in 64.5% of tumors and significantly correlated with estrogen receptor (ER), HER2, and p53 positivity.
- Patients with NS-positive tumors had significantly shorter disease-free survival.
- Co-positivity for NS and p53 was associated with a significantly poorer prognosis; NS was an independent prognostic indicator.
Conclusions:
- Nucleostemin (NS) may significantly influence breast cancer progression, particularly in conjunction with p53 alterations.
- NS status shows potential as a prognostic marker for luminal and HER2-type breast cancers.
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