Literature DB >> 27682830

The role of mutation analysis of the APC gene in the management of FAP patients. A controversial issue.

Concetta Dodaro, Carlo Grifasi, Jole Florio, Michele L Santangelo, Francesca Duraturo, Marina De Rosa, Paola Izzo, Andrea Renda.   

Abstract

BACKGROUND: A correlation between the location of mutation in the adenomatous polyposis coli (APC) gene and clinical manifestations of familial adenomatous polyposis (FAP) has repeatedly been reported. Some Authors suggest the use of mutational analysis as a guide to select the best surgical option in FAP patients. However, data coming from studies on large series have raised questions on this issue. The aim of this study is to discuss the role of the genetic tests in the management of FAP.
METHODS: A literature review was performed considering only peer-reviewed articles published between 1991-2015. All the studies examined the role of genetic as a guide for surgical management of FAP.
RESULTS: Of 363 articles identified, 21 were selected for full-text review. We found different positions with regard the use of genetic tests to determine surgical management of FAP. In particular, while consistent correlations between the APC mutation site and FAP phenotype were observed in large series, 8 studies reported a wide variation of genotypephenotype correlation in patients with the same mutation and they recommended that decisions regarding surgical strategy should be based not only on genotype but also on the clinical factors and the will of the patient who must be fully informed.
CONCLUSIONS: The decision on the type and the timing of surgery should be based on the assessment of many factors and genotype assessment should be used in combination with clinical data. KEY WORDS: Disease severity, Familial adenomatous polyposis, Genetic tests, Genotype-phenotype correlations, Surgical management.

Entities:  

Year:  2016        PMID: 27682830

Source DB:  PubMed          Journal:  Ann Ital Chir        ISSN: 0003-469X            Impact factor:   0.766


  6 in total

1.  Novel MSH2 splice-site mutation in a young patient with Lynch syndrome.

Authors:  Raffaella Liccardo; Marina De Rosa; Paola Izzo; Francesca Duraturo
Journal:  Mol Med Rep       Date:  2018-03-15       Impact factor: 2.952

2.  APC and MUTYH Analysis in FAP Patients: A Novel Mutation in APC Gene and Genotype-Phenotype Correlation.

Authors:  Giovanna D'Elia; Gemma Caliendo; Amelia Casamassimi; Michele Cioffi; Anna Maria Molinari; Maria Teresa Vietri
Journal:  Genes (Basel)       Date:  2018-06-27       Impact factor: 4.096

3.  Colorectal Cancer in the Elderly Patient: The Role of Neo-adjuvant Therapy.

Authors:  Concetta Anna Dodaro; Armando Calogero; Vincenzo Tammaro; Tommaso Pellegrino; Ruggero Lionetti; Silvia Campanile; Marsela Menkulazi; Massimo Ciccozzi; Anna Maria Iannicelli; Francesco Giallauria; Caterina Sagnelli
Journal:  Open Med (Wars)       Date:  2019-08-14

Review 4.  A Potential Role of IL-6/IL-6R in the Development and Management of Colon Cancer.

Authors:  Mimmo Turano; Francesca Cammarota; Francesca Duraturo; Paola Izzo; Marina De Rosa
Journal:  Membranes (Basel)       Date:  2021-04-24

5.  Significance of rare variants in genes involved in the pathogenesis of Lynch syndrome.

Authors:  Raffaella Liccardo; Matilde Lambiase; Antonio Nolano; Marina De Rosa; Paola Izzo; Francesca Duraturo
Journal:  Int J Mol Med       Date:  2022-04-27       Impact factor: 5.314

6.  Same MSH2 Gene Mutation But Variable Phenotypes in 2 Families With Lynch Syndrome: Two Case Reports and Review of Genotype-Phenotype Correlation.

Authors:  Raffaella Liccardo; Marina De Rosa; Francesca Duraturo
Journal:  Clin Med Insights Case Rep       Date:  2018-01-23
  6 in total

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