MMP-26 mRNA and Estrogen Receptor Alpha Co-expression in Normal and Pathological Endometrium
Pilka, R.1,3, Kudela, M.1, Eriksson, P.2, Casslén, B.3
1Gynekologicko porodnická klinika, FN a LF UP, Olomouc, přednosta prof. MUDr. M. Kudela, CSc. 2Oddělení výzkumu arteriosklerózy, Výzkumný ústav Krále Gustava V, Nemocnice Karolinska, Stockholm, Švédsko 3Gynekologicko porodnická klinika a Biomedicínské centrum, Univerzita v Lundu, Švédsko |
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Summary:
Objective: To examine the expression pattern of matrix metalloproteinase-26 (MMP-26) mRNAand
estrogen receptor-alpha (ER alpha) in normal, hyperplastic, premalignant and malignant endometrial
tissue.
Design: Experimental study.
Setting: Department of Obstetrics and Gynecology of the Palacky University Medical School and
University Hospital, Olomouc, Czech Republic, Department of Obstetrics and Gynecology, University
Hospital, Lund, Sweden, Atherosclerosis Research Unit, King Gustav V Research Institute, Karolinska
Hospital, Stockholm, Sweden.
Methods:We studied MMP-26 mRNA and ER alpha in 36 normal, 7 hyperplastic, 6 premalignant and 19
malignant endometrial samples. Based on histological examination, all normal specimens were classified
acccording to an ideal 28 day menstrual cycle as early, mid, and late proliferative phase, early, mid and late secretory phase and menstrual phase. Samples with hyperplasia were classified as simple or complex.
Premalignant samples were represented by complex hyperplasia with atypia. Malignant samples were
histologically classified as well, intermediately and poorly differentiated, respectively. Specimens were analyzed using in situ hybridization and real time PCR. ER alpha was localized by immunohistochemistry.
Results: Epithelial MMP-26mRNA expression was highest in the early secretory phase and in endometrial hyperplasia. Expression levels were low in the late secretory and menstrual phase and in malignant samples decreased gradually with dedifferentiation. Expression pattern of MMP-26 mRNA in normal, hyperplastic, premalignant and malignant endometrial tissue strongly co-variated with that of ER alpha.
Conclusion: Co-expression of MMP-26 and ER alpha in normal and pathological endometrial tissue suggests
possible regulation of MMP-26 gene by estrogen.
Key words:
endometrium, MMP-26, mRNA, regulation, ER
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