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Clinical significance of miR-140-5p and miR-193b expression in patients with breast cancer and relationship to IGFBP5
Authors:G?k?e Güllü   Irem Peker  Aptullah Haholu  Fatih Eren  Zafer Kü?ükodaci  Bülent Güle?   Hüseyin Baloglu  Can Erzik  Ayse ?zer  Mustafa Akkiprik
Affiliation:1.Department of Medical Biology, School of Medicine, Marmara University, Istanbul, Turkey.;2.Department of Pathology, Haydarpasa Training Hospital, Gülhane Military Medical Academy, Istanbul, Turkey.;3.Department of General Surgery, Haydarpasa Training Hospital, Gülhane Military Medical Academy, Istanbul, Turkey.;4.Department of Pathology, Anadolu Medical Center, Istanbul, Turkey.
Abstract:The functional role of IGFBP5 in breast cancer is complicated. Experimental andbioinformatics studies have shown that IGFBP5 is targeted by miR-140-5p and miR-193b,although this has not yet been proven in clinical samples. The aim of this study wasto evaluate the expression of miR-140-5p and miR-193b in breast cancer and adjacentnormal tissue and assess its correlation with IGFBP5 and the clinicopathologicalcharacteristics of the tumors. IGFBP5 protein expression was analyzedimmunohistochemically and IGFBP5, miR-140 and miR-193b mRNA expression levels wereanalyzed with real-time RT-PCR. Tumor tissue had higher miR-140-5p expression thanadjacent normal tissue (p = 0.015). Samples with no immunohistochemical staining forIGFBP5 showed increased miR-140-5p expression (p = 0.009). miR-140-5p expression waselevated in invasive ductal carcinomas (p = 0.002), whereas basal-like tumors haddecreased expression of miR-140-5p compared to other tumors (p = 0.008). Lymphnode-positive samples showed an approximately 13-fold increase in miR-140-5pexpression compared to lymph node-negative tissue (p = 0.049). These findings suggestthat miR-140-5p, but not miR-193b, could be an important determinant of IGFBP5expression and clinical phenotype in breast cancer patients. Further studies areneeded to clarify the expressional regulation of IGFBP5 by miR-140-5p.
Keywords:breast cancer   ER alpha   IGFBP5   micro RNA   miR-140   miR-193b
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