Oxytocin Receptor Expression is Associated with Estrogen Receptor Status in Breast Tumors

IF 0.6 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
T. S. Kalinina, V. V. Kononchuk, S. V. Sidorov, D. A. Obukhova, G. R. Abdullin, L. F. Gulyaeva
{"title":"Oxytocin Receptor Expression is Associated with Estrogen Receptor Status in Breast Tumors","authors":"T. S. Kalinina,&nbsp;V. V. Kononchuk,&nbsp;S. V. Sidorov,&nbsp;D. A. Obukhova,&nbsp;G. R. Abdullin,&nbsp;L. F. Gulyaeva","doi":"10.1134/S1990750821040065","DOIUrl":null,"url":null,"abstract":"<div><p>The oxytocin receptor (OXTR) plays an important role in childbirth, breastfeeding, and social interactions. Increasing evidence exists that OXTR is associated with the breast cancer (BC) initiation and progression. However, the mechanisms leading to its altered expression, the diagnostic or prognostic values of this receptor in BC are currently poorly understood. Here, we have evaluated the relative level of OXTR expression in BC samples (<i>n</i> = 107), and also investigated the effect of estradiol on its expression in MCF-7 and MDA-MB-231 cells. The level of OXTR expression was significantly lower in breast tumor tissue than in normal tissue obtained from the same patient. The OXTR expression depended on the status and expression of the estrogen receptor (ER): the level of OXTR mRNA was significantly lower in ER-negative BC samples compared to ER-positive BC samples. OXTR expression was also lower in samples from patients with luminal subtype with a low value of ER expression (0–5 score according to the IHC assay, Allred scoring) compared with samples with high ER expression (6–8 score). In luminal BC, OXTR expression was associated with the HER2 expression level: the OXTR mRNA level was higher in tumors with the HER2 IHC score of 1+ as compared to cases with the HER2 expression score of 2+, 3+. We also showed that estradiol increased the level of OXTR mRNA in MCF-7 cells, but not in ER-negative MDA-MB-231 cells. The data obtained indicate that changes in OXTR expression in BC tissues can be induced by increased ER expression. We found no association between OXTR and T or N stages and progesterone receptor expression.</p></div>","PeriodicalId":485,"journal":{"name":"Biochemistry (Moscow), Supplement Series B: Biomedical Chemistry","volume":"15 4","pages":"320 - 325"},"PeriodicalIF":0.6000,"publicationDate":"2021-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochemistry (Moscow), Supplement Series B: Biomedical Chemistry","FirstCategoryId":"2","ListUrlMain":"https://link.springer.com/article/10.1134/S1990750821040065","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 2

Abstract

The oxytocin receptor (OXTR) plays an important role in childbirth, breastfeeding, and social interactions. Increasing evidence exists that OXTR is associated with the breast cancer (BC) initiation and progression. However, the mechanisms leading to its altered expression, the diagnostic or prognostic values of this receptor in BC are currently poorly understood. Here, we have evaluated the relative level of OXTR expression in BC samples (n = 107), and also investigated the effect of estradiol on its expression in MCF-7 and MDA-MB-231 cells. The level of OXTR expression was significantly lower in breast tumor tissue than in normal tissue obtained from the same patient. The OXTR expression depended on the status and expression of the estrogen receptor (ER): the level of OXTR mRNA was significantly lower in ER-negative BC samples compared to ER-positive BC samples. OXTR expression was also lower in samples from patients with luminal subtype with a low value of ER expression (0–5 score according to the IHC assay, Allred scoring) compared with samples with high ER expression (6–8 score). In luminal BC, OXTR expression was associated with the HER2 expression level: the OXTR mRNA level was higher in tumors with the HER2 IHC score of 1+ as compared to cases with the HER2 expression score of 2+, 3+. We also showed that estradiol increased the level of OXTR mRNA in MCF-7 cells, but not in ER-negative MDA-MB-231 cells. The data obtained indicate that changes in OXTR expression in BC tissues can be induced by increased ER expression. We found no association between OXTR and T or N stages and progesterone receptor expression.

乳腺肿瘤中催产素受体表达与雌激素受体状态相关
催产素受体(OXTR)在分娩、母乳喂养和社会交往中起着重要作用。越来越多的证据表明,OXTR与乳腺癌的发生和发展有关。然而,导致其表达改变的机制,该受体在BC中的诊断或预后价值目前尚不清楚。在这里,我们评估了BC样本(n = 107)中OXTR的相对表达水平,并研究了雌二醇对MCF-7和MDA-MB-231细胞中OXTR表达的影响。OXTR在乳腺肿瘤组织中的表达水平明显低于同一患者的正常组织。OXTR的表达依赖于雌激素受体(ER)的状态和表达:雌激素受体阴性的BC样本中OXTR mRNA水平明显低于雌激素受体阳性的BC样本。与ER高表达的样本(6-8分)相比,低ER表达的luminal亚型患者样本(根据IHC检测,Allred评分为0-5分)的OXTR表达也较低。在管腔BC中,OXTR表达与HER2表达水平相关:HER2 IHC评分为1+的肿瘤中,OXTR mRNA水平高于HER2表达评分为2+、3+的肿瘤。我们还发现雌二醇增加了MCF-7细胞中OXTR mRNA的水平,但在er阴性的MDA-MB-231细胞中没有。所获得的数据表明,ER表达增加可诱导BC组织中OXTR表达的变化。我们没有发现OXTR与T或N分期和孕激素受体表达之间的关联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
1.10
自引率
0.00%
发文量
31
期刊介绍: Biochemistry (Moscow), Supplement Series B: Biomedical Chemistry   covers all major aspects of biomedical chemistry and related areas, including proteomics and molecular biology of (patho)physiological processes, biochemistry, neurochemistry, immunochemistry and clinical chemistry, bioinformatics, gene therapy, drug design and delivery, biochemical pharmacology, introduction and advertisement of new (biochemical) methods into experimental and clinical medicine. The journal also publishes review articles. All issues of the journal usually contain solicited reviews.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信