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Updated: Jul 10, 2026

Cell Population Analyses During Skin Carcinogenesis
Published on: August 21, 2013
Expression of minichromosome maintenance 5 protein in proliferative and malignant skin diseases
Houjun Liu1, Satoshi Takeuchi, Yoichi Moroi
1Department of Dermatology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Background:
The entire minichromosome maintenance (MCM) family (MCM2-7) play roles in the initiation and elongation of DNA replication. Many studies have demonstrated that MCM proteins may be better indicators of a wide variety of proliferative or cancer cells in malignant tissues.
Objectives:
To characterize the pattern and frequency of MCM5 expression in proliferative and malignant skin diseases in comparison with those of proliferating cell nuclear antigen (PCNA).
Methods:
Twelve normal skin specimens, 12 specimens of psoriasis, 21 specimens of bowenoid papulosis (BP), 16 specimens of Bowen's disease (BD), 38 specimens of skin squamous cell carcinoma (SCC), and 11 specimens of basal cell carcinoma (BCC) were subjected to immunohistochemical staining for MCM5 and PCNA. Results MCM5 protein was expressed in the lower layers of epidermis in psoriasis, while MCM5 protein were present throughout the tumor cells in BP, BD, and moderately/poorly differentiated SCC. MCM5 protein was preferentially expressed in the periphery of well-differentiated SCC or bigger nests of BCC, although some small nests of BCC seemingly showed diffuse staining patterns. The percentages of MCM5-positive cells were 15.7% in normal skin, 21.8% in psoriasis, 75.9% in BP, 83.8% in BD, 63.5% in well-differentiated SCC, 77.5% in moderately differentiated SCC, 79.8% in poorly differentiated SCC, and 21.2% in BCC in average. Well-differentiated SCC showed a significantly lower percentage of positive cells than did moderately differentiated SCC or poorly differentiated SCC. MCM5 staining basically show a similar staining pattern to that of PCNA, but more cells tended to be stained with MCM5 than with PCNA.
Conclusions:
Our results demonstrate pattern and frequency of MCM5 expression in various skin diseases and suggest that MCM5 may be a useful marker to detect cell proliferation in skin tissue sections.
Insights
Minichromosome maintenance 5 (MCM5) protein expression is frequent in proliferative and malignant skin conditions. MCM5 serves as a valuable marker for detecting cell proliferation in skin tissues, similar to proliferating cell nuclear antigen (PCNA).
Area of Science:
- Dermatology and Oncology
- Molecular Biology and Cell Cycle Regulation
Background:
- The minichromosome maintenance (MCM2-7) complex is crucial for DNA replication initiation and elongation.
- MCM proteins are recognized as potential biomarkers for proliferative and cancerous cells in various tissues.
Purpose of the Study:
- To investigate the expression patterns and frequency of MCM5 in normal and diseased skin.
- To compare MCM5 expression with proliferating cell nuclear antigen (PCNA) in proliferative and malignant skin conditions.
Main Methods:
- Immunohistochemical staining for MCM5 and PCNA was performed on skin specimens.
- Specimens included normal skin, psoriasis, bowenoid papulosis (BP), Bowen's disease (BD), squamous cell carcinoma (SCC), and basal cell carcinoma (BCC).
Main Results:
- MCM5 expression varied across skin conditions, observed in lower epidermal layers in psoriasis and throughout tumor cells in BP, BD, and SCC.
- MCM5 staining patterns generally mirrored PCNA, but MCM5 showed higher positive cell percentages.
- Significantly lower MCM5-positive cell percentages were noted in well-differentiated SCC compared to moderately/poorly differentiated SCC.
Conclusions:
- MCM5 exhibits distinct expression patterns in various proliferative and malignant skin diseases.
- MCM5 is a promising biomarker for assessing cell proliferation in skin tissue sections.
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