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本文引用的文献

1
Expression of IGF1R in normal breast tissue and subsequent risk of breast cancer.IGF1R 在正常乳腺组织中的表达与乳腺癌发生风险的关系。
Breast Cancer Res Treat. 2011 Jul;128(1):243-50. doi: 10.1007/s10549-010-1313-1. Epub 2011 Jan 1.
2
Ki67: a time-varying biomarker of risk of breast cancer in atypical hyperplasia.Ki67:非典型增生中乳腺癌风险的时变生物标志物。
Breast Cancer Res Treat. 2010 Jun;121(2):431-7. doi: 10.1007/s10549-009-0534-7. Epub 2009 Sep 23.
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Estrogen and progesterone receptor levels in nonneoplastic breast epithelium of breast cancer cases versus benign breast biopsy controls.乳腺癌病例与良性乳腺活检对照的非肿瘤性乳腺上皮中雌激素和孕激素受体水平。
BMC Cancer. 2008 May 8;8:130. doi: 10.1186/1471-2407-8-130.
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The role of oestrogen and progesterone receptors in human mammary development and tumorigenesis.雌激素和孕激素受体在人类乳腺发育及肿瘤发生中的作用。
Breast Cancer Res. 2002;4(5):197-201. doi: 10.1186/bcr452. Epub 2002 Jul 24.
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Low oestrogen receptor alpha expression in normal breast tissue underlies low breast cancer incidence in Japan.正常乳腺组织中雌激素受体α表达水平较低是日本乳腺癌发病率低的原因。
Lancet. 1999 Nov 20;354(9192):1787-8. doi: 10.1016/s0140-6736(99)04936-3.
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Murine mammary gland carcinogenesis is critically dependent on progesterone receptor function.小鼠乳腺癌发生严重依赖于孕激素受体功能。
Cancer Res. 1999 Sep 1;59(17):4276-84.
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Estrogen receptor expression of benign breast epithelium and its association with breast cancer.良性乳腺上皮的雌激素受体表达及其与乳腺癌的关联。
Cancer Res. 1994 Feb 15;54(4):993-7.
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Nuclear distribution of the Ki-67 antigen during the cell cycle: comparison with growth fraction in human breast cancer cells.细胞周期中Ki-67抗原的核分布:与人类乳腺癌细胞生长分数的比较
Cancer Res. 1989 Jun 1;49(11):2999-3006.
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Estrogen and progesterone receptors in the normal female breast.正常女性乳房中的雌激素和孕激素受体。
Cancer Res. 1991 Apr 1;51(7):1817-22.
10
c-myc, c-erbB-2, and Ki-67 expression in normal breast tissue and in invasive and noninvasive breast carcinoma.c-myc、c-erbB-2和Ki-67在正常乳腺组织、浸润性和非浸润性乳腺癌中的表达。
Cancer Res. 1992 May 1;52(9):2597-602.

雌激素受体、孕激素受体和Ki67在正常乳腺组织中的表达与后续患乳腺癌风险的关系。

Expression of estrogen receptor, progesterone receptor, and Ki67 in normal breast tissue in relation to subsequent risk of breast cancer.

作者信息

Oh Hannah, Eliassen A Heather, Wang Molin, Smith-Warner Stephanie A, Beck Andrew H, Schnitt Stuart J, Collins Laura C, Connolly James L, Montaser-Kouhsari Laleh, Polyak Kornelia, Tamimi Rulla M

机构信息

Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA; Channing Division of Network Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA; Department of Nutrition, Harvard T.H. Chan School of Public Health, Boston, MA, USA.

Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA; Channing Division of Network Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.

出版信息

NPJ Breast Cancer. 2016;2:16032-. doi: 10.1038/npjbcancer.2016.32. Epub 2016 Oct 26.

DOI:10.1038/npjbcancer.2016.32
PMID:28111631
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5243126/
Abstract

Although expression of estrogen receptor (ER), progesterone receptor (PR), and cell proliferation marker Ki67 serve as predictive and prognostic factors in breast cancers, little is known about their roles in normal breast tissue. Here in a nested case-control study within the Nurses' Health Studies (90 cases, 297 controls), we evaluated their expression levels in normal breast epithelium in relation to subsequent breast cancer risk among women with benign breast disease. Tissue microarrays were constructed using cores obtained from benign biopsies containing normal terminal duct lobular units and immunohistochemical stained for these markers. We found PR and Ki67 expression was non-significantly but positively associated with subsequent breast cancer risk, whereas ER expression was non-significantly inversely associated. After stratifying by lesion subtype, Ki67 was significantly associated with higher risk among women with proliferative lesions with atypical hyperplasia. However, given the small sample size, further studies are required to confirm these results.

摘要

尽管雌激素受体(ER)、孕激素受体(PR)的表达以及细胞增殖标志物Ki67在乳腺癌中可作为预测和预后因素,但它们在正常乳腺组织中的作用却鲜为人知。在护士健康研究中的一项巢式病例对照研究中(90例病例,297例对照),我们评估了良性乳腺疾病女性正常乳腺上皮中这些标志物的表达水平与后续患乳腺癌风险的关系。使用从包含正常终末导管小叶单位的良性活检组织中获取的组织芯构建组织微阵列,并对这些标志物进行免疫组织化学染色。我们发现PR和Ki67的表达与后续患乳腺癌风险呈非显著但正相关,而ER的表达呈非显著负相关。按病变亚型分层后,Ki67与伴有非典型增生的增殖性病变女性的较高风险显著相关。然而,鉴于样本量较小,需要进一步研究来证实这些结果。