Literature DB >> 2101719

The contribution of inherited predisposition to cancer incidence.

D Easton1, J Peto.   

Abstract

Only a small proportion of cancers, arising in inherited syndromes such as polyposis coli, have an unequivocally inherited basis. Nevertheless, most common cancers show familial clustering, much of which may be due to inherited predisposition. If so, there may be wide variation in genetic susceptibility to common cancers. The precise models of susceptibility are unclear, but for ovarian cancer and breast cancer there is some evidence that a small proportion of cases result from highly penetrant dominant genes. This has been confirmed recently for breast cancer by genetic linkage studies. Clear evidence for genetic susceptibility has been obtained for Hodgkin's disease and nasopharyngeal carcinoma, where the existence of susceptibility genes at the HLA locus has been demonstrated by linkage analysis. These genes could account for the majority of cases of these cancers. Identification of other cancer susceptibility genes should be possible, either directly using linkage analysis, or through identification of constitutional phenotypes related to cancer risk.

Entities:  

Mesh:

Year:  1990        PMID: 2101719

Source DB:  PubMed          Journal:  Cancer Surv        ISSN: 0261-2429


  21 in total

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Authors:  Elanie A Ostrander; Bo Johannesson
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2.  Testing for the breast cancer predisposition gene, BRCA1.

Authors:  R Eeles
Journal:  BMJ       Date:  1996-09-07

3.  The search for cancer risk factors: when can we stop looking?

Authors:  C B Begg
Journal:  Am J Public Health       Date:  2001-03       Impact factor: 9.308

4.  Try113His and His139Arg polymorphisms in the microsomal epoxide hydrolase gene are not associated with risk of breast cancer.

Authors:  Wen-Feng Gong; Wen He; Qiu-Ming Zhang; Bang-De Xiang; Liang Ma; Shan Huang; Tao Bai; Jian-Hong Zhong; Le-Qun Li
Journal:  Tumour Biol       Date:  2014-05-20

Review 5.  Epidemiology of Hodgkin's disease and non-Hodgkin's lymphoma.

Authors:  A J Swerdlow
Journal:  Eur J Nucl Med Mol Imaging       Date:  2003-05-07       Impact factor: 9.236

6.  Linkage analysis of 19 French breast cancer families, with five chromosome 17q markers.

Authors:  S Mazoyer; P Lalle; S A Narod; Y J Bignon; F Courjal; B Jamot; B Dutrillaux; D Stoppa-Lyonnett; H Sobol
Journal:  Am J Hum Genet       Date:  1993-04       Impact factor: 11.025

7.  Absence of linkage to the ataxia telangiectasia locus in familial breast cancer.

Authors:  R Wooster; D Ford; J Mangion; B A Ponder; J Peto; D F Easton; M R Stratton
Journal:  Hum Genet       Date:  1993-08       Impact factor: 4.132

8.  Clinical implications of E-cadherin associated hereditary diffuse gastric cancer.

Authors:  R C Fitzgerald; C Caldas
Journal:  Gut       Date:  2004-06       Impact factor: 23.059

9.  Risk factors for colorectal cancer in subjects with family history of the disease.

Authors:  E Fernandez; C La Vecchia; B D'Avanzo; E Negri; S Franceschi
Journal:  Br J Cancer       Date:  1997       Impact factor: 7.640

10.  Changes in psychological distress after cancer genetic counselling: a comparison of affected and unaffected women.

Authors:  A Bish; S Sutton; C Jacobs; S Levene; A Ramirez; S Hodgson
Journal:  Br J Cancer       Date:  2002-01-07       Impact factor: 7.640

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