Related Experiment Video
Updated: Jun 21, 2026

Platform for Quantitative Detection of Endometrial Immune Cells Based on Immunohistochemistry and Digital Image Analysis
Published on: October 13, 2023
Immunohistochemical pattern of protein P21, cyclin D1 and cyclin E in endometrial hyperplasia
Aleksandra Brucka1, Piotr Bartczak, Marzena Ratyńska
1Department of Stomatological Pathology, Medical University of Lodz, Lodz. alexbrucka@poczta.onet.pl
Purpose:
In our research we investigated immunohistochemical expression of cell cycle proteins protein p21, cyclin D1 and cyclin E in physiological endometrium (n = 15), hyperplastic endometrium (n = 61), and post hormone replacement therapy endometrium (n = 24).
Material And Methods:
We performed immunohistochemical analysis of selected cell cycle proteins in 100 specimens of human endometrium.
Results:
The average immunoexpression index scores in glandular endometrial cells (GES) and stromal endometrial cells (SEC) were respectively: for p21- GES: 11.8 +/- 17.19%; SEC: 9.31 +/- 17.15%; for cyclin D1- GES: 9.25 +/- 18.41%; SEC: 3.22 +/- 11.46%; for cyclin E: GES: 26.42 +/- 27.47%; SEC: 4.61 +/- 7.90%. Statistical analysis disclosed more intense p21 glandular immunoreactivity among women with endometrial hyperplasia in comparison to other subpopulations. In the case of assessment of cyclin D1 immunoreactivity, there was no statistical correlation between analysed parameters. The average cyclin E immunoreactivity in endometrial glandular cells was significantly higher (p = 0.003) in women with endometrial hyperplasia and correlated with age.
Conclusions:
Intensive immunoreactivity of cyclin E in glandular cells is typical for endometrial hyperplasia and can be treated as an objective indicator of this pathological process during histopathological diagnostic procedures. Immunoreactivity index of p21 and cyclin D1 is independent of the morphological pattern of human endometrium, patients' age and gynaecological history of patients.
Related Concept Videos
Positive Regulator Molecules
Abnormal Proliferation
Inhibition of Cdk Activity
Cellular Adaptation IV: Dysplasia and Metaplasia
