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Variances in the expression profile of histaminergic system in the endometroid endometrial cancer
* 1 , 1 , 1 , 1 , 1 , 1 , 2 , 1 , 1 , * 3, 4
1  Department of Histology, Cytophysiology and Embryology, Faculty of Medicine, University of Technology in Katowice, 41-800 Zabrze, Poland
2  Department of Gynecology and Obstetrics with Gynecologic Oncology, Ludwik Rydygier Memorial Specialized Hospital, 31-826 Kraków, Poland
3  Department of Histology, Cytophysiology and Embryology, Faculty of Medicine in Zabrze, Academy of Silesia, 40-555 Katowice, Poland
4  Department of Neurosurgery, 5th Military Clinical Hospital with the SP ZOZ Polyclinic in Krakow, 30-901 Krakow, Poland
Academic Editor: Jean Jacques Vanden Eynde

Abstract:

Endometroid endometrial cancer (EC) is one of the most common malignant tumors in women. Research has indicated a higher concentration of histamine and polyamine in the endometroid tissue in comparison with healthy tissue. The aim of the study was to evaluate changes in the expression pattern of genes related histaminergic system in endometrial samples and whole blood in women with endometroid endometrial cancer. The study group consisted of 30 women with endometroid endometrial cancer qualified for hysterectomy (G1 well-differentiated, 15 cases; G2 moderately differentiated, eight cases; and G3 poorly differentiated, seven cases). The control group included 30 women with no neoplastic changes during routine gynecological examinations. The molecular analysis consisted of microarray analysis of genes related to the histaminergic system It was shown that 10 from among 65 mRNAs connected with the histaminergic system differentiate the samples of tissue and blood obtained from patients with endometroid endometrial cancer in comparison with the control group (p < 0.05). It was observed that 2 mRNAs specifically differentiate samples G1 and G3 from the control, while gene 1 was distinctive for samples G3. On the other hand, HRH1, HRH3, and SLC23A2 were transcripts differentiating samples of endometroid endometrial cancer independent of either G or control. Along with the increase of the histopathological differentiation of the endometroid endometrial cancer the expression of the evaluated receptors was higher (C<G1>G2>G3; p < 0.05). The selected mRNAs seem to be promising as far as therapies targeted molecularly in the context of endometroid endometrial cancer.

Keywords: histaminergic system, mRNA, molecular amarker, endometroid endometrial cancer
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