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Breast cancer in sub-Saharan Africa: How does it relate to breast cancer in African-American women?

dc.contributor.authorFregene, Aleroen_US
dc.contributor.authorNewman, Lisa A.en_US
dc.date.accessioned2006-05-17T14:42:18Z
dc.date.available2006-05-17T14:42:18Z
dc.date.issued2005-04-15en_US
dc.identifier.citationFregene, Alero; Newman, Lisa A. (2005)."Breast cancer in sub-Saharan Africa: How does it relate to breast cancer in African-American women?." Cancer 103(8): 1540-1550. <http://hdl.handle.net/2027.42/39114>en_US
dc.identifier.issn0008-543Xen_US
dc.identifier.issn1097-0142en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/39114
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=15768434&dopt=citationen_US
dc.description.abstractBACKGROUND African-American women have had a lower incidence, yet higher mortality rate from breast cancer compared with White-American women. African-American women also have had a higher risk for early-onset, high-grade, node-positive, and hormone receptor-negative disease. Similar features have characterized hereditary breast cancer, prompting speculation that risk factors could be genetically transmitted. Further evaluation of this theory required the study of breast cancer among women from sub-Saharan Africa because of their shared ancestry with African-American women. METHODS Publications from 1988 to 2004 of English-language literature on breast cancer in Africa were reviewed. RESULTS Women from sub-Saharan Africa were found to have a low incidence of breast cancer. This was partly explained by a largely protective reproductive history, including late menarche, early menopause, high parity with prolonged breastfeeding, irregular menses, and fewer ovulatory cycles. The average age at diagnosis, however, was approximately 10 years younger than breast cancer patients of western nations, and disease stage distribution was shifted toward more advanced disease, which resulted in higher mortality rates. These features were found to be similar to data on breast cancer in African-American women. Mutations in BRCA1 and BRCA2 have been reported in African-American women, but the extent of the contribution of BRCA1 and BRCA2 to breast cancer burden in Africa was uncertain. Limited financial resources lead to suboptimal cancer data collection, as well as delayed diagnosis and treatment of many African breast cancer patients. CONCLUSIONS Parallels between breast cancer burdens of African-American and sub-Saharan–African women were provocative, indicating the need for further exploration of possible genetically transmitted features related to estrogen metabolism and/or breast cancer risk. Cancer 2005. © 2005 American Cancer Society.en_US
dc.format.extent241617 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherCancer Research, Oncology and Pathologyen_US
dc.titleBreast cancer in sub-Saharan Africa: How does it relate to breast cancer in African-American women?en_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelOncology and Hematologyen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Surgery, University of Michigan Comprehensive Cancer Center, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Surgery, University of Michigan Comprehensive Cancer Center, University of Michigan, Ann Arbor, Michigan ; Fax: 734-647-9647 ; University of Michigan, 1500 East Medical Center Drive, 3308 CGC, Ann Arbor, MI 48109en_US
dc.identifier.pmid15768434en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/39114/1/20978_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/cncr.20978en_US
dc.identifier.sourceCanceren_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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