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Cyclooxygenase-2 directly regulates gene expression of P450 Cyp19 aromatase promoter regions pII, pI.3 and pI.7 and estradiol production in human breast tumor cells.环氧化酶-2直接调节人乳腺肿瘤细胞中细胞色素P450 Cyp19芳香化酶启动子区域pII、pI.3和pI.7的基因表达以及雌二醇的产生。
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本文引用的文献

1
Obesity-associated systemic interleukin-6 promotes pre-adipocyte aromatase expression via increased breast cancer cell prostaglandin E2 production.肥胖相关的全身白细胞介素-6通过增加乳腺癌细胞前列腺素E2的产生来促进前脂肪细胞芳香化酶的表达。
Breast Cancer Res Treat. 2015 Jan;149(1):49-57. doi: 10.1007/s10549-014-3223-0. Epub 2014 Dec 5.
2
NSAID use reduces breast cancer recurrence in overweight and obese women: role of prostaglandin-aromatase interactions.非甾体抗炎药的使用可降低超重和肥胖女性的乳腺癌复发风险:与前列腺素-芳香酶相互作用有关。
Cancer Res. 2014 Aug 15;74(16):4446-57. doi: 10.1158/0008-5472.CAN-13-3603.
3
Obesity and survival in operable breast cancer patients treated with adjuvant anthracyclines and taxanes according to pathological subtypes: a pooled analysis.根据病理亚型,接受蒽环类药物和紫杉烷辅助治疗的可手术乳腺癌患者的肥胖与生存情况:一项汇总分析
Breast Cancer Res. 2013 Nov 6;15(6):R105. doi: 10.1186/bcr3572.
4
Deconvoluting the obesity and breast cancer link: secretome, soil and seed interactions.解析肥胖与乳腺癌的关联:分泌组、土壤与种子的相互作用。
J Mammary Gland Biol Neoplasia. 2013 Dec;18(3-4):267-75. doi: 10.1007/s10911-013-9301-9. Epub 2013 Oct 4.
5
Obesity enhances nongenomic estrogen receptor crosstalk with the PI3K/Akt and MAPK pathways to promote in vitro measures of breast cancer progression.肥胖增强了非基因组雌激素受体与PI3K/Akt和MAPK信号通路的相互作用,从而促进乳腺癌进展的体外检测。
Breast Cancer Res. 2013;15(4):R59. doi: 10.1186/bcr3453.
6
The predictive impact of body mass index on the efficacy of extended adjuvant endocrine treatment with anastrozole in postmenopausal patients with breast cancer: an analysis of the randomised ABCSG-6a trial.体重指数对绝经后乳腺癌患者接受阿那曲唑延长辅助内分泌治疗疗效的预测影响:随机 ABCSG-6a 试验分析。
Br J Cancer. 2013 Aug 6;109(3):589-96. doi: 10.1038/bjc.2013.367. Epub 2013 Jul 18.
7
Increased saturated fatty acids in obesity alter resolution of inflammation in part by stimulating prostaglandin production.肥胖症中饱和脂肪酸的增加部分通过刺激前列腺素的产生来改变炎症的消退。
J Immunol. 2013 Aug 1;191(3):1383-92. doi: 10.4049/jimmunol.1203369. Epub 2013 Jun 19.
8
Concurrent celecoxib with 5-fluorouracil/epirubicin/cyclophosphamide followed by docetaxel for stages II - III invasive breast cancer: the OOTR-N001 study.奥曲肽研究协作组 OOTR-N001 研究:在表柔比星/环磷酰胺/5-氟尿嘧啶联合多西紫杉醇治疗Ⅱ-Ⅲ期浸润性乳腺癌中,同期使用塞来昔布 请注意,该译文仅供参考,如果你需要更准确的翻译,建议咨询专业的翻译人员。
Expert Opin Investig Drugs. 2013 Mar;22(3):299-307. doi: 10.1517/13543784.2013.766715.
9
The relationship between body composition and response to neoadjuvant chemotherapy in women with operable breast cancer.可手术乳腺癌女性体成分与新辅助化疗反应的关系。
Oncologist. 2012;17(10):1240-5. doi: 10.1634/theoncologist.2012-0169. Epub 2012 Aug 17.
10
Obesity or overweight is associated with worse pathological response to neoadjuvant chemotherapy among Chinese women with breast cancer.肥胖或超重与中国乳腺癌女性新辅助化疗病理反应较差相关。
PLoS One. 2012;7(7):e41380. doi: 10.1371/journal.pone.0041380. Epub 2012 Jul 25.

靶向COX-2通路以改善肥胖乳腺癌患者群体的治疗反应。

Targeting the COX-2 Pathway to Improve Therapeutic Response in the Obese Breast Cancer Patient Population.

作者信息

Bowers Laura W, deGraffenried Linda A

机构信息

Department of Nutritional Sciences, University of Texas at Austin, 1400 Barbara Jordan Boulevard, R1800, Austin, TX 78723.

出版信息

Curr Pharmacol Rep. 2015 Oct 1;1(5):336-345. doi: 10.1007/s40495-015-0041-y. Epub 2015 Apr 22.

DOI:10.1007/s40495-015-0041-y
PMID:26442202
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4591549/
Abstract

Multiple studies have demonstrated that obesity is associated with a worse outcome for all breast cancer subtypes and that obese breast cancer patients do not respond as well as normal weight patients to aromatase inhibitor treatment and chemotherapy. While a number of mechanisms have been proposed to explain this link, recent studies have provided evidence that elevated local cyclooxygenase-2 (COX-2) expression and the resulting increase in prostaglandin E2 (PGE2) production may play an important role. COX-2 upregulation in breast tumors is associated with a poor prognosis, a connection generally attributed to PGE2's direct effects on apoptosis and invasion as well as its stimulation of pre-adipocyte aromatase expression and subsequent estrogen production. Research in this area has provided a strong foundation for the hypothesis that COX-2 signaling is involved in the obesity-breast cancer link, and further study regarding the role of COX-2 in this link is warranted.

摘要

多项研究表明,肥胖与所有乳腺癌亚型的不良预后相关,且肥胖乳腺癌患者对芳香化酶抑制剂治疗和化疗的反应不如正常体重患者。虽然已经提出了多种机制来解释这种联系,但最近的研究提供了证据表明,局部环氧化酶-2(COX-2)表达升高以及由此导致的前列腺素E2(PGE2)生成增加可能起重要作用。乳腺肿瘤中COX-2上调与预后不良相关,这种联系通常归因于PGE2对细胞凋亡和侵袭的直接作用,以及其对前脂肪细胞芳香化酶表达和随后雌激素生成的刺激。该领域的研究为COX-2信号传导参与肥胖与乳腺癌联系的假说提供了坚实基础,因此有必要进一步研究COX-2在这种联系中的作用。