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PMID: 15322516 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S. Review

Highly penetrant hereditary cancer syndromes.

Oncogene ·Vol. 23 ·No. 38 ·2004-08-23 ·Pages 6445-70

Nagy R, Sweet K, Eng C

Abstract

The past two decades have brought many important advances in our understanding of the hereditary susceptibility to cancer. Approximately 5-10% of all cancers are inherited, the majority in an autosomal dominant manner with incomplete penetrance. While this is a small fraction of the overall cancer burden worldwide, the molecular genetic discoveries that have resulted from the study of families with heritable cancer have not only changed the way these families are counselled and managed, but have shed light on molecular regulatory pathways important in sporadic tumour development as well. In this review, we consider 10 of the more highly penetrant cancer syndromes, with emphasis on those predisposing to breast, colon, and/or endocrine neoplasia. We discuss the prevalence, penetrance, and tumour spectrum associated with these syndromes, as well as their underlying genetic defects.

MeSH Terms
Breast Neoplasms/epidemiology,genetics Colonic Neoplasms/epidemiology,genetics Colorectal Neoplasms/epidemiology,genetics Endocrine Gland Neoplasms/epidemiology,genetics Genetic Predisposition to Disease/genetics Global Health Humans Incidence Neoplasms/epidemiology,genetics
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Nagy Rebecca
Clinical Cancer Genetics Program, Comprehensive Cancer Center, Division of Human Genetics, Department of Internal Medicine, The Ohio State University, Columbus 43221, USA. [email protected]
Sweet Kevin
Eng Charis
Article Info
Journal
Oncogene
Abbr.
Oncogene
ISSN
0950-9232
Published
2004-08-23
Pages
6445-70
Language
English
Region
England
NLM ID
8711562
Subset
IM
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