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   <subfield code="a">Hereditary prostate cancer as a feature of Lynch Syndrome</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Christina Bauer, Anna Ray, Bronwen Halstead-Nussloch, Robert Dekker, Victoria Raymond, Stephen Gruber, Kathleen Cooney]</subfield>
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   <subfield code="a">Lynch Syndrome is an autosomal dominant condition characterized by early onset colorectal cancer (CRC) and is associated with cancers of the gastrointestinal and reproductive tracts. Germline mutations in DNA mismatch repair (MMR) genes have been causally associated with cancers of Lynch Syndrome. We investigated the occurrence of prostate cancer (PCa) in families with a history of colorectal cancer to assess prostate cancer as a feature of the Lynch Syndrome spectrum. Family pedigrees containing at least one CRC case as well as those meeting guidelines for Lynch Syndrome were identified and tumors were requested from participants who underwent radical prostatectomy (RP). Selected families were analyzed for association with type of PCa and clinical characteristics of aggressive disease. Microsatellite Instability (MSI) analysis was preformed on available tumors and correlated to loss of expression in MMR genes by immunohistochemical (IHC) staining. 95 individuals were identified as members of potential Lynch Syndrome families who underwent RP and 35 tumors from 31 families were received for MSI analysis. Two tumors from two unrelated families with known MMR mutations were MSI-high and one additional case from a third family was MSI-low. The remainder of the prostate cancer cases demonstrated no evidence of MSI. PCa incidence in families enriched for hereditary PCa with a history of Lynch Syndrome cancers is not strongly suggestive of the presence of an MMR mutation. However prostate tumors in known MMR mutation carriers did display MSI and loss of gene expression suggesting that PCa may arise in Lynch Syndrome due to defective DNA mismatch repair.</subfield>
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   <subfield code="a">Springer Science+Business Media B.V., 2010</subfield>
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   <subfield code="u">Department of Epidemiology, University of Michigan School of Public Health, Ann Arbor, MI, USA</subfield>
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   <subfield code="a">Dekker</subfield>
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   <subfield code="a">Raymond</subfield>
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   <subfield code="a">Cooney</subfield>
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   <subfield code="u">Department of Internal Medicine, University of Michigan Medical School, 7216 CC, SPC 5948, 1500 East Medical Center Drive, 48109-5948, Ann Arbor, MI, USA</subfield>
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   <subfield code="t">Familial Cancer</subfield>
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   <subfield code="g">10/1(2011-03-01), 37-42</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
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