Hereditary colorectal cancer in the general population: From cancer registration to molecular diagnosis

M. Ponz De Leon, M. Pedroni, P. Benatti, A. Percesepe, C. Di Gregorio, M. Foroni, G. Rossi, M. Genuardi, G. Neri, F. Leonardi, A. Viel, E. Capozzi, M. Boiocchi, L. Roncucci

Research output: Contribution to journalArticle

Abstract

Background - Hereditary non-polyposis colorectal cancer (HNPCC) is one of the most common inherited disorders predisposing to cancer. The genes responsible for the disease have recently been cloned and characterised; their mutations induce a generalised genomic instability which is particularly evident at microsatellite loci (replication error (RER)+phenotype). Aims - To investigate how to select individuals and families in the general population who should be screened for constitutional mutations predisposing to colorectal cancer. Patients/Methods - Between 1984 and 1995, 1899 colorectal malignancies in 1831 patients were registered, and in 1721 of these (94%), family trees could be obtained. Patients and families were classified into five categories according to a more or less likely genetic basis: HNPCC; 'suspected' HNPCC; juvenile cases; aspecific cancer aggregation; sporadic cases. In 18 families with HNPCC as well as in 18 with suspected HNPCC, microsatellite instability in tumour tissues and constitutional mutations of two DNA mismatch repair genes (MSH2 and MLH1) could be evaluated. RER status was studied with five markers (BAT40, D2S123, D18S57, D173787, and BAT26) in paraffin embedded tissues. Germline mutations of MSH2 or MLH1 genes were assessed on DNA and RNA extracted from lymphomonocytic cells, using reverse transcription polymerase chain reaction, single strand conformation polymorphism analysis, and direct DNA sequencing. Results - HNPCC represented 2.6% and suspected HNPCC 4.6% of all registered colorectal neoplasms. Eleven out of 18 HNPCC families (61%) showed microsatellite instability as opposed to four (of 18) suspected HNPCC (22%; p

Original languageEnglish
Pages (from-to)32-38
Number of pages7
JournalGut
Volume45
Issue number1
Publication statusPublished - 1999

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Colorectal Neoplasms
Population
Neoplasms
Microsatellite Instability
Mutation
Genes
DNA Mismatch Repair
Germ-Line Mutation
Genomic Instability
Pedigree
DNA Sequence Analysis
Paraffin
Microsatellite Repeats
Reverse Transcription
RNA
Polymerase Chain Reaction
DNA

Keywords

  • Colorectal cancer
  • DNA repair genes
  • Hereditary non-polyposis colorectal cancer
  • Microsatellite loci
  • Mutation

ASJC Scopus subject areas

  • Gastroenterology

Cite this

Ponz De Leon, M., Pedroni, M., Benatti, P., Percesepe, A., Di Gregorio, C., Foroni, M., ... Roncucci, L. (1999). Hereditary colorectal cancer in the general population: From cancer registration to molecular diagnosis. Gut, 45(1), 32-38.

Hereditary colorectal cancer in the general population : From cancer registration to molecular diagnosis. / Ponz De Leon, M.; Pedroni, M.; Benatti, P.; Percesepe, A.; Di Gregorio, C.; Foroni, M.; Rossi, G.; Genuardi, M.; Neri, G.; Leonardi, F.; Viel, A.; Capozzi, E.; Boiocchi, M.; Roncucci, L.

In: Gut, Vol. 45, No. 1, 1999, p. 32-38.

Research output: Contribution to journalArticle

Ponz De Leon, M, Pedroni, M, Benatti, P, Percesepe, A, Di Gregorio, C, Foroni, M, Rossi, G, Genuardi, M, Neri, G, Leonardi, F, Viel, A, Capozzi, E, Boiocchi, M & Roncucci, L 1999, 'Hereditary colorectal cancer in the general population: From cancer registration to molecular diagnosis', Gut, vol. 45, no. 1, pp. 32-38.
Ponz De Leon M, Pedroni M, Benatti P, Percesepe A, Di Gregorio C, Foroni M et al. Hereditary colorectal cancer in the general population: From cancer registration to molecular diagnosis. Gut. 1999;45(1):32-38.
Ponz De Leon, M. ; Pedroni, M. ; Benatti, P. ; Percesepe, A. ; Di Gregorio, C. ; Foroni, M. ; Rossi, G. ; Genuardi, M. ; Neri, G. ; Leonardi, F. ; Viel, A. ; Capozzi, E. ; Boiocchi, M. ; Roncucci, L. / Hereditary colorectal cancer in the general population : From cancer registration to molecular diagnosis. In: Gut. 1999 ; Vol. 45, No. 1. pp. 32-38.
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abstract = "Background - Hereditary non-polyposis colorectal cancer (HNPCC) is one of the most common inherited disorders predisposing to cancer. The genes responsible for the disease have recently been cloned and characterised; their mutations induce a generalised genomic instability which is particularly evident at microsatellite loci (replication error (RER)+phenotype). Aims - To investigate how to select individuals and families in the general population who should be screened for constitutional mutations predisposing to colorectal cancer. Patients/Methods - Between 1984 and 1995, 1899 colorectal malignancies in 1831 patients were registered, and in 1721 of these (94{\%}), family trees could be obtained. Patients and families were classified into five categories according to a more or less likely genetic basis: HNPCC; 'suspected' HNPCC; juvenile cases; aspecific cancer aggregation; sporadic cases. In 18 families with HNPCC as well as in 18 with suspected HNPCC, microsatellite instability in tumour tissues and constitutional mutations of two DNA mismatch repair genes (MSH2 and MLH1) could be evaluated. RER status was studied with five markers (BAT40, D2S123, D18S57, D173787, and BAT26) in paraffin embedded tissues. Germline mutations of MSH2 or MLH1 genes were assessed on DNA and RNA extracted from lymphomonocytic cells, using reverse transcription polymerase chain reaction, single strand conformation polymorphism analysis, and direct DNA sequencing. Results - HNPCC represented 2.6{\%} and suspected HNPCC 4.6{\%} of all registered colorectal neoplasms. Eleven out of 18 HNPCC families (61{\%}) showed microsatellite instability as opposed to four (of 18) suspected HNPCC (22{\%}; p",
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T1 - Hereditary colorectal cancer in the general population

T2 - From cancer registration to molecular diagnosis

AU - Ponz De Leon, M.

AU - Pedroni, M.

AU - Benatti, P.

AU - Percesepe, A.

AU - Di Gregorio, C.

AU - Foroni, M.

AU - Rossi, G.

AU - Genuardi, M.

AU - Neri, G.

AU - Leonardi, F.

AU - Viel, A.

AU - Capozzi, E.

AU - Boiocchi, M.

AU - Roncucci, L.

PY - 1999

Y1 - 1999

N2 - Background - Hereditary non-polyposis colorectal cancer (HNPCC) is one of the most common inherited disorders predisposing to cancer. The genes responsible for the disease have recently been cloned and characterised; their mutations induce a generalised genomic instability which is particularly evident at microsatellite loci (replication error (RER)+phenotype). Aims - To investigate how to select individuals and families in the general population who should be screened for constitutional mutations predisposing to colorectal cancer. Patients/Methods - Between 1984 and 1995, 1899 colorectal malignancies in 1831 patients were registered, and in 1721 of these (94%), family trees could be obtained. Patients and families were classified into five categories according to a more or less likely genetic basis: HNPCC; 'suspected' HNPCC; juvenile cases; aspecific cancer aggregation; sporadic cases. In 18 families with HNPCC as well as in 18 with suspected HNPCC, microsatellite instability in tumour tissues and constitutional mutations of two DNA mismatch repair genes (MSH2 and MLH1) could be evaluated. RER status was studied with five markers (BAT40, D2S123, D18S57, D173787, and BAT26) in paraffin embedded tissues. Germline mutations of MSH2 or MLH1 genes were assessed on DNA and RNA extracted from lymphomonocytic cells, using reverse transcription polymerase chain reaction, single strand conformation polymorphism analysis, and direct DNA sequencing. Results - HNPCC represented 2.6% and suspected HNPCC 4.6% of all registered colorectal neoplasms. Eleven out of 18 HNPCC families (61%) showed microsatellite instability as opposed to four (of 18) suspected HNPCC (22%; p

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KW - DNA repair genes

KW - Hereditary non-polyposis colorectal cancer

KW - Microsatellite loci

KW - Mutation

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