Literature DB >> 25064638

Increased prevalence of lung, breast, and pancreatic cancers in addition to melanoma risk in families bearing the cyclin-dependent kinase inhibitor 2A mutation: implications for genetic counseling.

Miriam Potrony1, Joan Anton Puig-Butillé2, Paula Aguilera1, Celia Badenas2, Cristina Carrera1, Josep Malvehy1, Susana Puig3.   

Abstract

BACKGROUND: Cyclin-dependent kinase inhibitor 2A (CDKN2A) is the major high-risk susceptibility gene for melanoma.
OBJECTIVE: We sought to evaluate the effect of CDKN2A mutations in Spanish patients with a high risk of developing melanoma and the association with clinical and family history features.
METHODS: A cross-sectional study design was used to analyze the CDKN2A impact in 702 Spanish patients with a high risk of developing melanoma.
RESULTS: The CDKN2A mutation prevalence was 8.5% in patients with sporadic multiple primary melanoma and 14.1% in familial melanoma. Number of cases in the family, number of primary melanomas, and age of onset were associated with the presence of CDKN2A mutation. Having a CDKN2A mutation in the family increased the prevalence of other cancers (prevalence ratio [PR] 2.99, P=.012) and prevalence of pancreatic (PR 2.97, P=.006), lung (PR 3.04, P<.001), and breast (PR 2.19, P=.018) cancers but not nephrourologic or colon cancer. LIMITATIONS: Smoking status was not assessed in the individuals with lung cancer.
CONCLUSIONS: Melanoma-prone families with mutations in CDKN2A have an increased prevalence of a broad spectrum of cancers including lung, pancreatic, and breast cancer. This information should be included in genetic counseling and cancer prevention programs for CDKN2A mutation carriers.
Copyright © 2014 American Academy of Dermatology, Inc. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  CDKN2A; breast cancer; genetic counseling; lung cancer; melanoma; pancreatic cancer; prevention; risk; smoking

Mesh:

Substances:

Year:  2014        PMID: 25064638      PMCID: PMC4250348          DOI: 10.1016/j.jaad.2014.06.036

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN: 0190-9622            Impact factor:   11.527


  41 in total

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Authors:  D C Whiteman; A C Green
Journal:  Int J Dermatol       Date:  1999-07       Impact factor: 2.736

Review 2.  Meta-analysis of risk factors for cutaneous melanoma: I. Common and atypical naevi.

Authors:  Sara Gandini; Francesco Sera; Maria Sofia Cattaruzza; Paolo Pasquini; Damiano Abeni; Peter Boyle; Carmelo Francesco Melchi
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Authors:  P Ghiorzo; P Ciotti; M Mantelli; A Heouaine; P Queirolo; M L Rainero; C Ferrari; P L Santi; R De Marchi; A Farris; F Ajmar; P Bruzzi; G Bianchi-Scarrà
Journal:  Int J Cancer       Date:  1999-11-12       Impact factor: 7.396

4.  Germline p16 mutations in familial melanoma.

Authors:  C J Hussussian; J P Struewing; A M Goldstein; P A Higgins; D S Ally; M D Sheahan; W H Clark; M A Tucker; N C Dracopoli
Journal:  Nat Genet       Date:  1994-09       Impact factor: 38.330

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Authors:  S Puig; A Ruiz; T Castel; V Volpini; J Malvehy; F Cardellach; M Lynch; J M Mascaro; X Estivill
Journal:  Hum Genet       Date:  1997-12       Impact factor: 4.132

7.  Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study Group.

Authors:  N Soufir; M F Avril; A Chompret; F Demenais; J Bombled; A Spatz; D Stoppa-Lyonnet; J Bénard; B Bressac-de Paillerets
Journal:  Hum Mol Genet       Date:  1998-02       Impact factor: 6.150

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9.  Mutations of the CDKN2/p16INK4 gene in Australian melanoma kindreds.

Authors:  G J Walker; C J Hussussian; J F Flores; J M Glendening; F G Haluska; N C Dracopoli; N K Hayward; J W Fountain
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Authors:  J Siemiatycki; D Krewski; E Franco; M Kaiserman
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