Source:http://linkedlifedata.com/resource/pubmed/id/14673037
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
24
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pubmed:dateCreated |
2003-12-15
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pubmed:abstractText |
Despite recognition that second malignant neoplasms (SMNs) contribute significantly to mortality after the successful treatment of Hodgkin's disease (HD), little is known about the molecular events leading to secondary tumors. Factors contributing to second cancer risk include the carcinogenic effects of ionizing radiation and chemotherapy, in combination with possible host susceptibility. To clarify whether host genetic factors contribute to secondary tumorigenesis, we performed mutational analyses of the TP53, BRCA1, and BRCA2 tumor suppressor genes in a cohort of 44 HD patients developing one or more SMN.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0732-183X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
21
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4505-9
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:14673037-Adult,
pubmed-meshheading:14673037-DNA Mutational Analysis,
pubmed-meshheading:14673037-Female,
pubmed-meshheading:14673037-Genes, BRCA1,
pubmed-meshheading:14673037-Genes, BRCA2,
pubmed-meshheading:14673037-Genes, p53,
pubmed-meshheading:14673037-Genetic Predisposition to Disease,
pubmed-meshheading:14673037-Hodgkin Disease,
pubmed-meshheading:14673037-Humans,
pubmed-meshheading:14673037-Male,
pubmed-meshheading:14673037-Middle Aged,
pubmed-meshheading:14673037-Neoplasms, Second Primary
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pubmed:year |
2003
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pubmed:articleTitle |
TP53, BRCA1, and BRCA2 tumor suppressor genes are not commonly mutated in survivors of Hodgkin's disease with second primary neoplasms.
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pubmed:affiliation |
Department of Pediatric Oncology, Children's Hospital of Philadelphia, PA, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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