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患有两种乳腺癌或卵巢癌的女性的癌症风险:遗传性癌症易感性线索

Cancer risks in women with 2 breast or ovarian cancers: clues to genetic cancer susceptibility.

作者信息

Evans H S, Lewis C M, Robinson D, Bell C M, Møller H, Hodgson S V

机构信息

Thames Cancer Registry, Division of Medicine, Guy's, King's and St. Thomas' School of Medicine, London, United Kingdom.

出版信息

Int J Cancer. 2001 Dec 1;94(5):758-9. doi: 10.1002/ijc.1534.

DOI:10.1002/ijc.1534
PMID:11745474
Abstract

Women diagnosed with 2 cancers of the breast and/or ovary are at higher risk of developing subsequent cancers. Using registrations from the Thames Cancer Registry, we quantified the risks at different cancer sites. Increased risks were found for cancers that are part of the BRCA1 and BRCA2 tumour spectrum: oropharyngeal cancer, malignant melanoma of the skin (BRCA2) and colon cancer (BRCA1). We also found significantly increased risks of myeloid leukaemia (probably due to radiotherapy) and of cancer of the corpus uteri (which may be due to hormonal factors).

摘要

被诊断患有乳腺癌和/或卵巢癌的女性患后续癌症的风险更高。利用泰晤士癌症登记处的登记数据,我们对不同癌症部位的风险进行了量化。发现与BRCA1和BRCA2肿瘤谱相关的癌症风险增加:口咽癌、皮肤恶性黑色素瘤(BRCA2相关)和结肠癌(BRCA1相关)。我们还发现髓系白血病(可能由于放疗)和子宫体癌(可能由于激素因素)的风险显著增加。

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Cancer risks in women with 2 breast or ovarian cancers: clues to genetic cancer susceptibility.患有两种乳腺癌或卵巢癌的女性的癌症风险:遗传性癌症易感性线索
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引用本文的文献

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Absence of founder BRCA1 and BRCA2 mutations in cutaneous malignant melanoma patients of Ashkenazi origin.阿什肯纳兹血统的皮肤恶性黑色素瘤患者中不存在始祖BRCA1和BRCA2突变。
Fam Cancer. 2009;8(1):29-32. doi: 10.1007/s10689-008-9206-8. Epub 2008 Aug 5.
2
The BRCA1/2 pathway prevents hematologic cancers in addition to breast and ovarian cancers.除了乳腺癌和卵巢癌,BRCA1/2 通路还能预防血液系统癌症。
BMC Cancer. 2007 Aug 6;7:152. doi: 10.1186/1471-2407-7-152.
3
Prognostic value of BRCA1 mutations in familial breast cancer patients affected by a second primary cancer.
Fam Cancer. 2007;6(4):409-13. doi: 10.1007/s10689-007-9139-7. Epub 2007 May 23.
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Hereditary breast and ovarian cancer: review and future perspectives.遗传性乳腺癌和卵巢癌:综述与未来展望
J Mol Med (Berl). 2006 Jan;84(1):16-28. doi: 10.1007/s00109-005-0696-7. Epub 2005 Nov 11.