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Expression of <jats:styled-content style=\"fixed-case\">MT<\/jats:styled-content>1 in neoplastic cells seems to increase the efficacy of melatonin's oncostatic activity. The purpose of this study was to determine the distribution and the intensity of <jats:styled-content style=\"fixed-case\">MT<\/jats:styled-content>1 expression in breast cancer cells and to correlate it with clinicopathological factors. Immunohistochemical studies (<jats:styled-content style=\"fixed-case\">IHC<\/jats:styled-content>) were conducted on 190 cases of invasive ductal breast carcinomas (<jats:styled-content style=\"fixed-case\">IDC<\/jats:styled-content>) and molecular studies were performed on 29 cases of frozen tumor fragments and selected breast cancer cell lines. Most of the studied tumors manifested a membranous\/cytoplasmic <jats:styled-content style=\"fixed-case\">IHC<\/jats:styled-content> expression of <jats:styled-content style=\"fixed-case\">MT<\/jats:styled-content>1. In <jats:styled-content style=\"fixed-case\">IDC<\/jats:styled-content>, the <jats:styled-content style=\"fixed-case\">MT<\/jats:styled-content>1 expression was higher than in fibrocystic breast disease. <jats:styled-content style=\"fixed-case\">MT<\/jats:styled-content>1 expression was higher in estrogen receptor positive (<jats:styled-content style=\"fixed-case\">ER<\/jats:styled-content>+) and <jats:styled-content style=\"fixed-case\">HER<\/jats:styled-content>2 positive (<jats:styled-content style=\"fixed-case\">HER<\/jats:styled-content>2+) tumors. Triple negative tumors (<jats:styled-content style=\"fixed-case\">TN<\/jats:styled-content>) manifested the lowest <jats:styled-content style=\"fixed-case\">MT<\/jats:styled-content>1 expression level. The lowest <jats:styled-content style=\"fixed-case\">MT<\/jats:styled-content>1 protein expression level was noted in the <jats:styled-content style=\"fixed-case\">TN<\/jats:styled-content> breast cancer cell line <jats:styled-content style=\"fixed-case\">MDA<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">MB<\/jats:styled-content>\u2010231 compared with <jats:styled-content style=\"fixed-case\">ER<\/jats:styled-content>+ cell lines <jats:styled-content style=\"fixed-case\">MCF<\/jats:styled-content>\u20107 and <jats:styled-content style=\"fixed-case\">SK<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">BR<\/jats:styled-content>\u20103. <jats:styled-content style=\"fixed-case\">MT<\/jats:styled-content>1 m<jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content> expression was negatively correlated with the malignancy grade of the studied <jats:styled-content style=\"fixed-case\">IDC<\/jats:styled-content> cases. Moreover, higher <jats:styled-content style=\"fixed-case\">MT<\/jats:styled-content>1 expression was associated with patients' longer overall survival (<jats:styled-content style=\"fixed-case\">OS<\/jats:styled-content>) in the group of <jats:styled-content style=\"fixed-case\">ER<\/jats:styled-content>+ breast cancers and treated with tamoxifen. Multivariate analysis indicated that <jats:styled-content style=\"fixed-case\">MT<\/jats:styled-content>1 was an independent prognostic factor in the <jats:styled-content style=\"fixed-case\">ER<\/jats:styled-content>+ tumors for <jats:styled-content style=\"fixed-case\">OS<\/jats:styled-content> and event\u2010free survival in the <jats:styled-content style=\"fixed-case\">ER<\/jats:styled-content>+ tumors. The results of this study may point to a potential prognostic and therapeutic significance of <jats:styled-content style=\"fixed-case\">MT<\/jats:styled-content>1 in <jats:styled-content style=\"fixed-case\">IDC<\/jats:styled-content>.<\/jats:p>","DOI":"10.1111\/jpi.12032","type":"journal-article","created":{"date-parts":[[2012,12,13]],"date-time":"2012-12-13T20:11:55Z","timestamp":1355429515000},"page":"334-345","source":"Crossref","is-referenced-by-count":57,"title":["Expression of melatonin receptor <scp>MT<\/scp>1 in cells of human invasive ductal breast carcinoma"],"prefix":"10.1111","volume":"54","author":[{"given":"Karolina","family":"Jablonska","sequence":"first","affiliation":[{"name":"Department of Histology and Embryology Wroclaw Medical University Wroclaw Poland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Bartosz","family":"Pula","sequence":"additional","affiliation":[{"name":"Department of Histology and Embryology Wroclaw Medical University Wroclaw 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Poland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Aleksandra","family":"Ambicka","sequence":"additional","affiliation":[{"name":"Department of Tumor Pathology Centre of Oncology Maria Sklodowska\u2010Curie Memorial Institute, Cracow Branch Cracow Poland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Marzena","family":"Podhorska\u2010Okolow","sequence":"additional","affiliation":[{"name":"Department of Histology and Embryology Wroclaw Medical University Wroclaw Poland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Maciej","family":"Ugorski","sequence":"additional","affiliation":[{"name":"Department of Biochemistry, Pharmacology and Toxicology Wroclaw University of Environmental and Life Sciences Wroclaw Poland"},{"name":"Laboratory of Glycobiology and Cellular Interactions Institute of Immunology and Experimental Therapy Polish Academy of Sciences Wroclaw 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