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http://purl.uniprot.org/citations/34449552http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/34449552http://www.w3.org/2000/01/rdf-schema#comment"Uterine fibroids are the most common mesenchymal uterine neoplasms; their prevalence is estimated in 40%-60% of women under 35 and in 70%-80% of women over 50 years of age. The current research aims to focus on the etiopathogenesis of uterine fibroids, the factors that affect their growth, and markers with diagnostic and prognostic properties. The MCM (minichromosome maintenance) protein family consists of peptides whose primary function is participation in the molecular mechanism of creating replication forks while regulating DNA synthesis. The aim of this work was to determine the proliferative potential of uterine fibroid cells based on the expression of the Ki-67 antigen and the MCMs-i.e., MCM-3, MCM-5, and MCM-7. In addition, the expression of estrogen (ER) and progesterone (PgR) receptors was evaluated and correlated with the expression of the abovementioned observations. Ultimately, received results were analyzed in terms of clinical and pathological data.

Materials and methods

In forty-four cases of uterine fibroids, immunohistochemical reactions were performed. A tissue microarray (TMA) technique was utilized and analyzed cases were assessed in triplicate. Immunohistochemistry was performed using antibodies against Ki-67 antigen, ER, PgR, MCM-3, MCM-5, and MCM-8 on an automated staining platform. Reactions were digitalized by a histologic scanner and quantified utilizing dedicated software for nuclear analysis. Assessment was based on quantification expression of the three histiospots, each representing one case in TMA.

Results

In the study group (uterine fibroids), statistically significant stronger expression of all the investigated MCMs was observed, as compared to the control group. In addition, moderate and strong positive correlations were found between all tested proliferative markers. The expression of the MCM-7 protein also correlated positively with ER and PgR. With regard to clinical and pathological data, there was a negative correlation between the expression of MCMs and the number of both pregnancies and births. Significant reductions in MCM-5 and MCM-7 expression were observed in the group of women receiving oral hormonal contraceptives, while smoking women showed an increase in MCM-7, ER, and PgR.

Conclusions

Uterine fibroid cells have greater proliferative potential, as evaluated by expression of the Ki-67 antigen and MCMs, than unaltered myometrial cells of the uterine corpus. The expression of MCM-7 was found to have strong or moderate correlations in all assessed relations. In the context of the clinical data, as well evident proliferative potential of MCMs, further studies are strongly recommended."xsd:string
http://purl.uniprot.org/citations/34449552http://purl.org/dc/terms/identifier"doi:10.3390/cimb43020058"xsd:string
http://purl.uniprot.org/citations/34449552http://purl.uniprot.org/core/author"Hirnle L."xsd:string
http://purl.uniprot.org/citations/34449552http://purl.uniprot.org/core/author"Kobierzycki C."xsd:string
http://purl.uniprot.org/citations/34449552http://purl.uniprot.org/core/author"Rubisz P."xsd:string
http://purl.uniprot.org/citations/34449552http://purl.uniprot.org/core/date"2021"xsd:gYear
http://purl.uniprot.org/citations/34449552http://purl.uniprot.org/core/name"Curr Issues Mol Biol"xsd:string
http://purl.uniprot.org/citations/34449552http://purl.uniprot.org/core/pages"802-817"xsd:string
http://purl.uniprot.org/citations/34449552http://purl.uniprot.org/core/title"The Immunohistochemical Expression of MCM-3, -5, and -7 Proteins in the Uterine Fibroids."xsd:string
http://purl.uniprot.org/citations/34449552http://purl.uniprot.org/core/volume"43"xsd:string
http://purl.uniprot.org/citations/34449552http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/34449552
http://purl.uniprot.org/citations/34449552http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/34449552
http://purl.uniprot.org/uniprot/#_A0A0S2Z441-mappedCitation-34449552http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34449552
http://purl.uniprot.org/uniprot/#_A0A0S2Z4T1-mappedCitation-34449552http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34449552
http://purl.uniprot.org/uniprot/#_A0A0S2Z492-mappedCitation-34449552http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34449552
http://purl.uniprot.org/uniprot/#_A0A0S2Z4A5-mappedCitation-34449552http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34449552
http://purl.uniprot.org/uniprot/#_A0A499FHX9-mappedCitation-34449552http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34449552
http://purl.uniprot.org/uniprot/#_B3KUD7-mappedCitation-34449552http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34449552
http://purl.uniprot.org/uniprot/#_B4DDF5-mappedCitation-34449552http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34449552
http://purl.uniprot.org/uniprot/#_B4DVK5-mappedCitation-34449552http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34449552
http://purl.uniprot.org/uniprot/#_B2R7C5-mappedCitation-34449552http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34449552
http://purl.uniprot.org/uniprot/#_B3KVF0-mappedCitation-34449552http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34449552
http://purl.uniprot.org/uniprot/#_B2RBA6-mappedCitation-34449552http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34449552
http://purl.uniprot.org/uniprot/#_B4DQ39-mappedCitation-34449552http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34449552
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