Adiposity Results in Metabolic and Inflammation Differences in Premenopausal and Postmenopausal Women Consistent with the Difference in Breast Cancer Risk.

IF 3 4区 医学 Q3 Biochemistry, Genetics and Molecular Biology
H Zhao, J Wang, D Fang, O Lee, R T Chatterton, V Stearns, S A Khan, S E Bulun
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引用次数: 11

Abstract

Obesity is associated with increased risk of breast cancer in postmenopausal but not in premenopausal women. Many factors may be responsible for this difference. The aim of this study was to determine the mechanisms by which the genes related to the AMPK pathway, inflammation, and estrogen actions are affected by adiposity in breast tissue with the objective of identifying differences that may explain the different breast cancer risk in premenopausal and postmenopausal women. Random fine needle aspirates (rFNAs) of breast tissue were collected from 57 premenopausal and 55 postmenopausal women and were classified as normal weight, overweight, or obese. Expression levels of 21 target genes were determined using a TaqMan Low Density Array procedure. Breast tissue estradiol levels were measured by a liquid chromatography-tandem mass spectrometry procedure, and serum estradiol and follicle-stimulating hormone (FSH) were measured by a radioimmunoassay and an enzyme-linked immunosorbent assay, respectively. We found that in postmenopausal women, serum and tissue estradiol levels were increased in those who were overweight, and serum FSH levels were decreased in obese status. Interestingly, RPS6KB1, an AMPK downstream-responsive gene for protein synthesis and cell growth, and estrogen receptor α (encoded by the ESR1 gene) and its target gene GATA3 were significantly decreased in rFNA of premenopausal, obese women. In postmenopausal women, RPS6KB1, ESR1, and GATA3 expression remained unchanged in relation to adiposity. However, prostaglandin-endoperoxide synthase 2 (PTGS2), cyclin D1 (CCND1), and another ESR1 target gene, TFF1, were elevated in rFNA of obese postmenopausal women. Thus, as bodyweight increases, gene expression is indicative of increased proliferation in postmenopausal women but decreased proliferation in premenopausal women. Overall, our data reveal a novel process by which obesity promotes the risk of breast cancer in postmenopausal but not premenopausal women.

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肥胖导致绝经前和绝经后妇女的代谢和炎症差异与乳腺癌风险的差异一致。
肥胖与绝经后妇女患乳腺癌的风险增加有关,但与绝经前妇女无关。造成这种差异的因素可能有很多。本研究的目的是确定与AMPK通路、炎症和雌激素作用相关的基因受乳腺组织肥胖影响的机制,目的是确定可能解释绝经前和绝经后妇女乳腺癌风险差异的差异。随机收集57名绝经前和55名绝经后妇女的乳腺组织细针抽吸(rFNAs),并将其分为正常体重、超重或肥胖。使用TaqMan低密度阵列程序检测21个靶基因的表达水平。采用液相色谱-串联质谱法测定乳腺组织雌二醇水平,分别采用放射免疫法和酶联免疫吸附法测定血清雌二醇和促卵泡激素(FSH)。我们发现,在绝经后的妇女中,超重的妇女血清和组织雌二醇水平升高,而肥胖的妇女血清FSH水平降低。有趣的是,在绝经前肥胖女性的rFNA中,参与蛋白合成和细胞生长的AMPK下游响应基因RPS6KB1、雌激素受体α(由ESR1基因编码)及其靶基因GATA3显著降低。在绝经后妇女中,RPS6KB1、ESR1和GATA3的表达与肥胖的关系保持不变。然而,前列腺素内过氧化物合成酶2 (PTGS2)、细胞周期蛋白D1 (CCND1)和另一个ESR1靶基因TFF1在肥胖绝经后妇女的rFNA中升高。因此,随着体重的增加,基因表达表明绝经后妇女的增殖增加,而绝经前妇女的增殖减少。总的来说,我们的数据揭示了一个新的过程,即肥胖增加了绝经后而不是绝经前妇女患乳腺癌的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Hormones & Cancer
Hormones & Cancer ONCOLOGY-ENDOCRINOLOGY & METABOLISM
CiteScore
4.60
自引率
0.00%
发文量
0
期刊介绍: Hormones and Cancer is a unique multidisciplinary translational journal featuring basic science, pre-clinical, epidemiological, and clinical research papers. It covers all aspects of the interface of Endocrinology and Oncology. Thus, the journal covers two main areas of research: Endocrine tumors (benign & malignant tumors of hormone secreting endocrine organs) and the effects of hormones on any type of tumor. We welcome all types of studies related to these fields, but our particular attention is on translational aspects of research. In addition to basic, pre-clinical, and epidemiological studies, we encourage submission of clinical studies including those that comprise small series of tumors in rare endocrine neoplasias and/or negative or confirmatory results provided that they significantly enhance our understanding of endocrine aspects of oncology. The journal does not publish case studies.
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