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本文引用的文献

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Genomics, Endoscopy, and Control of Gastroesophageal Cancers: A Perspective.基因组学、内窥镜检查与食管癌的控制:一种观点
Cell Mol Gastroenterol Hepatol. 2017 Feb 20;3(3):359-366. doi: 10.1016/j.jcmgh.2017.02.005. eCollection 2017 May.
2
The relationship between statins and breast cancer prognosis varies by statin type and exposure time: a meta-analysis.他汀类药物与乳腺癌预后的关系因他汀类药物类型和暴露时间而异:一项荟萃分析。
Breast Cancer Res Treat. 2017 Jul;164(1):1-11. doi: 10.1007/s10549-017-4246-0. Epub 2017 Apr 21.
3
An Adolescent and Early Adulthood Dietary Pattern Associated with Inflammation and the Incidence of Breast Cancer.一种与炎症及乳腺癌发病率相关的青少年和青年期饮食模式。
Cancer Res. 2017 Mar 1;77(5):1179-1187. doi: 10.1158/0008-5472.CAN-16-2273.
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Cancer Statistics, 2017.《2017 年癌症统计》
CA Cancer J Clin. 2017 Jan;67(1):7-30. doi: 10.3322/caac.21387. Epub 2017 Jan 5.
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RNA Sequencing Identifies Transcriptionally Viable Gene Fusions in Esophageal Adenocarcinomas.RNA测序鉴定食管腺癌中具有转录活性的基因融合
Cancer Res. 2016 Oct 1;76(19):5628-5633. doi: 10.1158/0008-5472.CAN-16-0979. Epub 2016 Aug 8.
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Association Between Germline Mutation in VSIG10L and Familial Barrett Neoplasia.VSIG10L 种系突变与家族性 Barrett 肿瘤的相关性。
JAMA Oncol. 2016 Oct 1;2(10):1333-1339. doi: 10.1001/jamaoncol.2016.2054.
7
ACG Clinical Guideline: Diagnosis and Management of Barrett's Esophagus.美国胃肠病学会临床指南:巴雷特食管的诊断与管理
Am J Gastroenterol. 2016 Jan;111(1):30-50; quiz 51. doi: 10.1038/ajg.2015.322. Epub 2015 Nov 3.
8
Metabolic syndrome and breast cancer risk: a case-cohort study nested in a multicentre italian cohort.代谢综合征与乳腺癌风险:一项纳入意大利多中心队列的病例队列研究
PLoS One. 2015 Jun 1;10(6):e0128891. doi: 10.1371/journal.pone.0128891. eCollection 2015.
9
Adolescent meat intake and breast cancer risk.青少年肉类摄入量与乳腺癌风险。
Int J Cancer. 2015 Apr 15;136(8):1909-20. doi: 10.1002/ijc.29218. Epub 2014 Oct 3.
10
Surveillance of Barrett's esophagus and mortality from esophageal adenocarcinoma: a population-based cohort study.巴雷特食管的监测与食管腺癌死亡率:一项基于人群的队列研究。
Am J Gastroenterol. 2014 Aug;109(8):1215-22. doi: 10.1038/ajg.2014.156. Epub 2014 Jul 1.

散发性和家族性巴雷特食管与乳腺癌的关联。

Association of sporadic and familial Barrett's esophagus with breast cancer.

作者信息

Chan M Q, Blum A E, Chandar A K, Emmons A M L Kieber, Shindo Y, Brock W, Falk G W, Canto M I, Wang J S, Iyer P G, Shaheen N J, Grady W M, Abrams J A, Thota P N, Guda K K, Chak A

机构信息

University Hospitals Cleveland Medical Center, Cleveland, Ohio.

Louis Stokes VA Medical Center, Cleveland, Ohio.

出版信息

Dis Esophagus. 2018 Apr 1;31(4). doi: 10.1093/dote/doy007.

DOI:10.1093/dote/doy007
PMID:29528378
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6005759/
Abstract

Barrett's esophagus (BE) is the only known precursor to esophageal adenocarcinoma (EAC). Based on striking aggregation of breast cancer and BE/EAC within families as well as shared risk factors and molecular mechanisms of carcinogenesis, we hypothesized that BE may be associated with breast cancer. Pedigree analysis of families identified prospectively at multiple academic centers as part of the Familial Barrett's Esophagus Consortium (FBEC) was reviewed and families with aggregation of BE/EAC and breast cancer are reported. Additionally, using a matched case-control study design, we compared newly diagnosed BE cases in Caucasian females with breast cancer (cases) to Caucasian females without breast cancer (controls) who had undergone upper endoscopy (EGD). Two familial pedigrees, meeting a stringent inclusion criterion, manifested familial aggregation of BE/EAC and breast cancer in an autosomal dominant inheritance pattern with incomplete penetrance. From January 2008 to October 2016, 2812 breast cancer patient charts were identified, of which 213 were Caucasian females who underwent EGD. Six of 213 (2.82%) patients with breast cancer had pathology-confirmed BE, compared to 1 of 241 (0.41%) controls (P-value < 0.05). Selected families with BE/EAC show segregation of breast cancer. A breast cancer diagnosis is marginally associated with BE. We postulate a common susceptibility between BE/EAC and breast cancer.

摘要

巴雷特食管(BE)是已知的食管腺癌(EAC)唯一前驱病变。基于乳腺癌与BE/EAC在家族中的显著聚集现象以及致癌作用的共同风险因素和分子机制,我们推测BE可能与乳腺癌相关。对作为家族性巴雷特食管联盟(FBEC)一部分在多个学术中心前瞻性确定的家族进行系谱分析,并报告BE/EAC和乳腺癌聚集的家族。此外,采用匹配病例对照研究设计,我们将新诊断的患有乳腺癌的白人女性BE病例(病例组)与接受上消化道内镜检查(EGD)的无乳腺癌的白人女性(对照组)进行比较。两个符合严格纳入标准的家族系谱显示BE/EAC和乳腺癌以常染色体显性遗传模式且具有不完全外显率的形式出现家族聚集。从2008年1月至2016年10月,共识别出2812份乳腺癌患者病历,其中213例为接受EGD检查的白人女性。213例(2.82%)乳腺癌患者中有6例经病理证实患有BE,而241例(0.41%)对照组中有1例(P值<0.05)。选定的BE/EAC家族显示出乳腺癌的分离现象。乳腺癌诊断与BE存在微弱关联。我们推测BE/EAC和乳腺癌之间存在共同易感性。