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Significance of RCC2, Rac1 and p53 Expression in Breast Infiltrating Ductal Carcinoma; An Immunohistochemical Study
Aiat Shaban Hemida1, Reham Ahmed Abdelaziz2, Moshira Mohammed Abd El-Wahed1
1Department of Pathology, Faculty of Medicine, Menoufia University, Shebin El Kom, Egypt.
Iranian Journal of Pathology
|August 9, 2024
Summary
Regulator of chromosome condensation 2 (RCC2) and RAS-related C3 botulinum toxin substrate 1 (Rac1) are highly expressed in breast cancer and correlate with poor prognostic factors. Their association with aggressive tumor features suggests potential as therapeutic targets.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Regulator of chromosome condensation 2 (RCC2) and RAS-related C3 botulinum toxin substrate 1 (Rac1) are implicated in breast cancer cell proliferation and migration.
- A p53/RCC2/Rac1 signaling pathway is proposed to regulate colon cancer metastasis, but its role in breast cancer remains under-investigated.
Purpose of the Study:
- To investigate the immunohistochemical expression and correlations of RCC2, Rac1, and p53 in breast infiltrating ductal carcinoma (IDC).
Main Methods:
- Immunohistochemical staining for RCC2, Rac1, and p53 on 120 breast IDC specimens.
- Statistical analysis to determine correlations between the expression of these markers.
Main Results:
- High expression of RCC2 (96.7%), Rac1 (100%), and p53 (27.5%) was observed.
- RCC2, Rac1, and p53 expression correlated with poor prognostic indicators including frequent mitoses, high Ki-67, lymphovascular invasion, and advanced tumor stage.
- A significant direct correlation was found between all three markers.
Conclusions:
- Elevated RCC2, Rac1, and p53 levels in breast IDC suggest a role in tumor progression.
- RCC2 and Rac1 may serve as predictive indicators for aggressive breast tumors, potentially benefiting from targeted therapies.

