Balakan Ozan, Kalender Mehmet Emin, Suner Ali, Cengiz Beyhan, Oztuzcu Serdar, Bayraktar Recep, Borazan Ersin, Babacan Taner, Camci Celaletdin
Department of Internal Medicine, Kahramanmaras Sutcu Imam University, Kahramanmaraş, Turkey.
Department of Medical Oncology, Gaziantep University, School of Medicine, Gaziantep, Turkey.
Med Sci Monit. 2014 Aug 12;20:1419-25. doi: 10.12659/MSM.890459.
Urotensin II is a vasoactive polypeptide. It is known that some vasoactive polypeptides are produced and secreted by tumor cells, and act as a paracrine growth stimulant. The aim of this study was to examine the relationship between urotensin II and its receptor's messenger RNA expression in breast cancer.
MATERIAL/METHODS: Fifty-nine women with breast cancer were included in this study. The median age was 48 years. The relationships between urotensin II and urotensin II receptor mRNA expressions, which were derived from fresh breast cancer tissues and adjacent normal breast tissues, and clinical and pathological parameters, were assessed.
We found expressions of urotensin II mRNA and its receptor in 55 of 59 breast cancer tissues and in 55 of 59 normal breast tissues. We found a positive significant correlation between urotensin II and its receptor (p=0.001, r=0.632), and found a negative, but insignificant, correlation between urotensin II and age (p=0.038, r=-0.281). Urotensin II levels were higher in the premenopausal group compared to the postmenopausal group (p<0.05). The mean urotensin II receptor expression was higher in the premenopausal group (p<0.05) compared to the postmenopausal group, and its expression was also higher in the group without extra-nodal invasion compared to that of the group with extra-nodal invasion (p=0.001). Urotensin II levels were higher in the group without lymphatic invasion compared to the group with lymphatic invasion (p=0.048).
This study is the first in the English medical literature to determine the urotensin II and its receptor mRNA expressions in breast cancer tissues. Consequently, urotensin II seems be associated with menopausal status, and extra-nodal and lymphatic invasion.
尾加压素II是一种血管活性多肽。已知一些血管活性多肽由肿瘤细胞产生并分泌,作为旁分泌生长刺激因子发挥作用。本研究的目的是检测尾加压素II及其受体信使核糖核酸在乳腺癌中的表达关系。
材料/方法:本研究纳入了59例乳腺癌女性患者。中位年龄为48岁。评估了来自新鲜乳腺癌组织和相邻正常乳腺组织的尾加压素II及其受体信使核糖核酸表达之间的关系,以及临床和病理参数。
我们在59例乳腺癌组织中的55例以及59例正常乳腺组织中的55例中发现了尾加压素II信使核糖核酸及其受体的表达。我们发现尾加压素II与其受体之间存在显著正相关(p = 0.001,r = 0.632),并且发现尾加压素II与年龄之间存在负相关,但无统计学意义(p = 0.038,r = -0.281)。绝经前组的尾加压素II水平高于绝经后组(p < 0.05)。绝经前组的尾加压素II受体平均表达高于绝经后组(p < 0.05),并且在无结外侵犯组中的表达也高于有结外侵犯组(p = 0.001)。无淋巴侵犯组的尾加压素II水平高于有淋巴侵犯组(p = 0.048)。
本研究是英文医学文献中首次测定乳腺癌组织中尾加压素II及其受体信使核糖核酸表达的研究。因此,尾加压素II似乎与绝经状态、结外和淋巴侵犯有关。