Immunohistochemical Expression of IRE1 and PERK in Breast Cancer: Associations With Clinicopathological Characteristics and Survival Outcomes
- Stefanos Flindris 1,2, Georgios Markozannes 3, Chrysoula Margioula-Siarkou 2, Nikolaos Tsiaras 4, Georgia Margioula-Siarkou 2, Christos Chalitsios 3, Eleni Sakellariou 4, Konstantinos Flindris 5, Effrosyni Styliara 6, Minas Paschopoulos 1, Stamatios Petousis 2, Iordanis Navrozoglou 1, Konstantinos Dinas 2
- 1Department of Obstetrics and Gynecology, University Hospital of Ioannina, University of Ioannina, Ioannina, Greece.
- 22nd Department of Obstetrics and Gynecology, General Hospital of Thessaloniki "Hippokration", Aristotle University of Thessaloniki, Thessaloniki, Greece.
- 3Department of Hygiene and Epidemiology, University of Ioannina, Medical School, Ioannina, Greece.
- 4Department of Pathology, General Hospital of Thessaloniki "Hippokration", Thessaloniki, Greece.
- 5Department of Ophthalmology, General Hospital of Ioannina "G. Hatzikosta", Ioannina, Greece.
- 6Department of Radiology, University Hospital of Ioannina, University of Ioannina, Ioannina, Greece.
- 0Department of Obstetrics and Gynecology, University Hospital of Ioannina, University of Ioannina, Ioannina, Greece.
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View abstract on PubMed
Summary
This summary is machine-generated.High expression of IRE1 and PERK (inositol-requiring enzyme 1 and PKR-like endoplasmic reticulum kinase) is linked to aggressive breast cancer and poorer survival. These findings highlight the unfolded protein response
Area Of Science
- Oncology
- Molecular Biology
- Cancer Research
Background
- The unfolded protein response (UPR) pathway, involving IRE1 and PERK, plays a role in cellular stress.
- Dysregulation of UPR components like IRE1 and PERK is implicated in various cancers, including breast cancer.
Purpose Of The Study
- To evaluate the immunohistochemical expression of IRE1 and PERK in breast cancer.
- To investigate the association between IRE1 and PERK expression and clinicopathological characteristics.
- To explore the relationship between IRE1 and PERK expression and patient survival outcomes.
Main Methods
- Immunohistochemistry was used to analyze IRE1 and PERK expression in 72 breast cancer specimens and 16 controls.
- Statistical analyses, including Kaplan-Meier curves and Cox proportional hazard models, were employed.
- Associations with clinicopathological variables, hormone receptor status, tumor markers, and survival were assessed.
Main Results
- IRE1 and PERK expression were significantly elevated in breast cancer tissues compared to controls (p<0.001).
- High IRE1/PERK expression correlated with aggressive tumor features: older age, higher grade, advanced TNM stage, positive hormone receptors, HER2 positivity, and increased Ki-67.
- High IRE1 and PERK expression were associated with increased mortality risk and worse survival (HR=12.19, p=0.05 for IRE1; HR=12.10, p=0.04 for PERK).
Conclusions
- Elevated IRE1 and PERK expression are biomarkers for aggressive breast cancer phenotypes.
- The UPR pathway is crucial in breast cancer carcinogenesis and progression.
- Targeting IRE1 and PERK may offer therapeutic strategies for breast cancer.
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