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Germline CDH1 deletions in hereditary diffuse gastric cancer families

Identifieur interne : 001201 ( Istex/Curation ); précédent : 001200; suivant : 001202

Germline CDH1 deletions in hereditary diffuse gastric cancer families

Auteurs : Carla Oliveira [Portugal] ; Janine Senz [Canada] ; Pardeep Kaurah [Canada] ; Hugo Pinheiro [Portugal] ; Remo Sanges [Italie] ; Anne Haegert [Canada] ; Giovanni Corso [Italie] ; Jan Schouten [Pays-Bas] ; Rebecca Fitzgerald [Royaume-Uni] ; Holger Vogelsang ; Gisela Keller [Allemagne] ; Sarah Dwerryhouse [Royaume-Uni] ; Donna Grimmer [Royaume-Uni] ; Suet-Feung Chin [Royaume-Uni] ; Han-Kwang Yang [Corée du Sud] ; Charles E. Jackson [États-Unis] ; Raquel Seruca [Portugal] ; Franco Roviello [Italie] ; Elia Stupka [Italie] ; Carlos Caldas [Royaume-Uni] ; David Huntsman [Canada]

Source :

RBID : ISTEX:B9ADA09039B1D374381A8FA829BEC4470EE6605F

Abstract

Germline CDH1 point or small frameshift mutations can be identified in 3050 of hereditary diffuse gastric cancer (HDGC) families. We hypothesized that CDH1 genomic rearrangements would be found in HDGC and identified 160 families with either two gastric cancers in first-degree relatives and with at least one diffuse gastric cancer (DGC) diagnosed before age 50, or three or more DGC in close relatives diagnosed at any age. Sixty-seven carried germline CDH1 point or small frameshift mutations. We screened germline DNA from the 93 mutation negative probands for large genomic rearrangements by Multiplex Ligation-Dependent Probe Amplification. Potential deletions were validated by RTPCR and breakpoints cloned using a combination of oligo-CGH-arrays and long-range-PCR. In-silico analysis of the CDH1 locus was used to determine a potential mechanism for these rearrangements. Six of 93 (6.5) previously described mutation negative HDGC probands, from low GC incidence populations (UK and North America), carried genomic deletions (UK and North America). Two families carried an identical deletion spanning 193 593 bp, encompassing the full CDH3 sequence and CDH1 exons 1 and 2. Other deletions affecting exons 1, 2, 15 and/or 16 were identified. The statistically significant over-representation of Alus around breakpoints indicates it as a likely mechanism for these deletions. When all mutations and deletions are considered, the overall frequency of CDH1 alterations in HDGC is 46 (73/160). CDH1 large deletions occur in 4 of HDGC families by mechanisms involving mainly non-allelic homologous recombination in Alu repeat sequences. As the finding of pathogenic CDH1 mutations is useful for management of HDGC families, screening for deletions should be offered to at-risk families.

Url:
DOI: 10.1093/hmg/ddp046

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ISTEX:B9ADA09039B1D374381A8FA829BEC4470EE6605F

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Holger Vogelsang
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<name sortKey="Seruca, Raquel" sort="Seruca, Raquel" uniqKey="Seruca R" first="Raquel" last="Seruca">Raquel Seruca</name>
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<name sortKey="Roviello, Franco" sort="Roviello, Franco" uniqKey="Roviello F" first="Franco" last="Roviello">Franco Roviello</name>
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<name sortKey="Caldas, Carlos" sort="Caldas, Carlos" uniqKey="Caldas C" first="Carlos" last="Caldas">Carlos Caldas</name>
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<title level="a">Germline CDH1 deletions in hereditary diffuse gastric cancer families</title>
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<name sortKey="Oliveira, Carla" sort="Oliveira, Carla" uniqKey="Oliveira C" first="Carla" last="Oliveira">Carla Oliveira</name>
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<name sortKey="Senz, Janine" sort="Senz, Janine" uniqKey="Senz J" first="Janine" last="Senz">Janine Senz</name>
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<name sortKey="Kaurah, Pardeep" sort="Kaurah, Pardeep" uniqKey="Kaurah P" first="Pardeep" last="Kaurah">Pardeep Kaurah</name>
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<name sortKey="Sanges, Remo" sort="Sanges, Remo" uniqKey="Sanges R" first="Remo" last="Sanges">Remo Sanges</name>
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<name sortKey="Haegert, Anne" sort="Haegert, Anne" uniqKey="Haegert A" first="Anne" last="Haegert">Anne Haegert</name>
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<name sortKey="Corso, Giovanni" sort="Corso, Giovanni" uniqKey="Corso G" first="Giovanni" last="Corso">Giovanni Corso</name>
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<name sortKey="Schouten, Jan" sort="Schouten, Jan" uniqKey="Schouten J" first="Jan" last="Schouten">Jan Schouten</name>
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<name sortKey="Fitzgerald, Rebecca" sort="Fitzgerald, Rebecca" uniqKey="Fitzgerald R" first="Rebecca" last="Fitzgerald">Rebecca Fitzgerald</name>
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<name sortKey="Vogelsang, Holger" sort="Vogelsang, Holger" uniqKey="Vogelsang H" first="Holger" last="Vogelsang">Holger Vogelsang</name>
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<name sortKey="Keller, Gisela" sort="Keller, Gisela" uniqKey="Keller G" first="Gisela" last="Keller">Gisela Keller</name>
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<country xml:lang="fr">Allemagne</country>
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<name sortKey="Dwerryhouse, Sarah" sort="Dwerryhouse, Sarah" uniqKey="Dwerryhouse S" first="Sarah" last="Dwerryhouse">Sarah Dwerryhouse</name>
<affiliation wicri:level="1">
<mods:affiliation>Department of Oncology, University of Cambridge, Cambridge CB2 0QQ, UK</mods:affiliation>
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Department of Oncology, University of Cambridge, Cambridge CB2 0QQ</wicri:regionArea>
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<name sortKey="Grimmer, Donna" sort="Grimmer, Donna" uniqKey="Grimmer D" first="Donna" last="Grimmer">Donna Grimmer</name>
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<mods:affiliation>Cancer Research UK Cambridge Research Institute, Li Ka Shing Centre, Cambridge CB2 0RE, UK</mods:affiliation>
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Cancer Research UK Cambridge Research Institute, Li Ka Shing Centre, Cambridge CB2 0RE</wicri:regionArea>
</affiliation>
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<name sortKey="Chin, Suet Feung" sort="Chin, Suet Feung" uniqKey="Chin S" first="Suet-Feung" last="Chin">Suet-Feung Chin</name>
<affiliation wicri:level="1">
<mods:affiliation>Cancer Research UK Cambridge Research Institute, Li Ka Shing Centre, Cambridge CB2 0RE, UK</mods:affiliation>
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Cancer Research UK Cambridge Research Institute, Li Ka Shing Centre, Cambridge CB2 0RE</wicri:regionArea>
</affiliation>
</author>
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<name sortKey="Yang, Han Kwang" sort="Yang, Han Kwang" uniqKey="Yang H" first="Han-Kwang" last="Yang">Han-Kwang Yang</name>
<affiliation wicri:level="1">
<mods:affiliation>Department of Surgery and Cancer Research Institute, Seoul National University College of Medicine, Seoul 151-742, South Korea</mods:affiliation>
<country xml:lang="fr">Corée du Sud</country>
<wicri:regionArea>Department of Surgery and Cancer Research Institute, Seoul National University College of Medicine, Seoul 151-742</wicri:regionArea>
</affiliation>
</author>
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<name sortKey="Jackson, Charles E" sort="Jackson, Charles E" uniqKey="Jackson C" first="Charles E." last="Jackson">Charles E. Jackson</name>
<affiliation>
<mods:affiliation>Department of Surgery and</mods:affiliation>
</affiliation>
<affiliation wicri:level="1">
<mods:affiliation>Department of Medical Genetics, Henry Ford Hospital, Detroit, MI 48202, USA</mods:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Medical Genetics, Henry Ford Hospital, Detroit, MI 48202</wicri:regionArea>
</affiliation>
</author>
<author>
<name sortKey="Seruca, Raquel" sort="Seruca, Raquel" uniqKey="Seruca R" first="Raquel" last="Seruca">Raquel Seruca</name>
<affiliation wicri:level="1">
<mods:affiliation>Institute of Molecular Pathology and Immunology, University of Porto (IPATIMUP), 4200-465 Porto, Portugal</mods:affiliation>
<country xml:lang="fr">Portugal</country>
<wicri:regionArea>Institute of Molecular Pathology and Immunology, University of Porto (IPATIMUP), 4200-465 Porto</wicri:regionArea>
</affiliation>
<affiliation wicri:level="1">
<mods:affiliation>Faculty of Medicine, University of Porto, 4200-319 Porto, Portugal</mods:affiliation>
<country xml:lang="fr">Portugal</country>
<wicri:regionArea>Faculty of Medicine, University of Porto, 4200-319 Porto</wicri:regionArea>
</affiliation>
</author>
<author>
<name sortKey="Roviello, Franco" sort="Roviello, Franco" uniqKey="Roviello F" first="Franco" last="Roviello">Franco Roviello</name>
<affiliation wicri:level="1">
<mods:affiliation>Department of Human Pathology and Oncology, Section of Surgical Oncology, Translational Research Laboratory, Istituto Toscano Tumori (ITT), University of Siena, 53100 Siena, Italy</mods:affiliation>
<country xml:lang="fr">Italie</country>
<wicri:regionArea>Department of Human Pathology and Oncology, Section of Surgical Oncology, Translational Research Laboratory, Istituto Toscano Tumori (ITT), University of Siena, 53100 Siena</wicri:regionArea>
</affiliation>
<affiliation wicri:level="1">
<mods:affiliation>Division of Surgical Oncology, University of Siena, 53100 Siena, Italy</mods:affiliation>
<country xml:lang="fr">Italie</country>
<wicri:regionArea>Division of Surgical Oncology, University of Siena, 53100 Siena</wicri:regionArea>
</affiliation>
</author>
<author>
<name sortKey="Stupka, Elia" sort="Stupka, Elia" uniqKey="Stupka E" first="Elia" last="Stupka">Elia Stupka</name>
<affiliation wicri:level="1">
<mods:affiliation>CBM S.c.r.l., AREA Science Park, Basovizza 34012, Trieste, Italy</mods:affiliation>
<country xml:lang="fr">Italie</country>
<wicri:regionArea>CBM S.c.r.l., AREA Science Park, Basovizza 34012, Trieste</wicri:regionArea>
</affiliation>
</author>
<author>
<name sortKey="Caldas, Carlos" sort="Caldas, Carlos" uniqKey="Caldas C" first="Carlos" last="Caldas">Carlos Caldas</name>
<affiliation wicri:level="1">
<mods:affiliation>Department of Oncology, University of Cambridge, Cambridge CB2 0QQ, UK</mods:affiliation>
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Department of Oncology, University of Cambridge, Cambridge CB2 0QQ</wicri:regionArea>
</affiliation>
<affiliation wicri:level="1">
<mods:affiliation>Cancer Research UK Cambridge Research Institute, Li Ka Shing Centre, Cambridge CB2 0RE, UK</mods:affiliation>
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Cancer Research UK Cambridge Research Institute, Li Ka Shing Centre, Cambridge CB2 0RE</wicri:regionArea>
</affiliation>
</author>
<author>
<name sortKey="Huntsman, David" sort="Huntsman, David" uniqKey="Huntsman D" first="David" last="Huntsman">David Huntsman</name>
<affiliation wicri:level="1">
<mods:affiliation>Hereditary Cancer Program and the Centre for Translational and Applied Genomics, British Columbia Cancer Agency, Vancouver, Canada V5Z 4E6</mods:affiliation>
<country>Canada</country>
<wicri:regionArea>Hereditary Cancer Program and the Centre for Translational and Applied Genomics, British Columbia Cancer Agency, Vancouver</wicri:regionArea>
</affiliation>
<affiliation wicri:level="1">
<mods:affiliation>E-mail: dhuntsma@bccancer.bc.ca</mods:affiliation>
<country wicri:rule="url">Canada</country>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series>
<title level="j">Human Molecular Genetics</title>
<idno type="ISSN">0964-6906</idno>
<idno type="eISSN">1460-2083</idno>
<imprint>
<publisher>Oxford University Press</publisher>
<date type="published" when="2009-05-01">2009-05-01</date>
<biblScope unit="volume">18</biblScope>
<biblScope unit="issue">9</biblScope>
<biblScope unit="page" from="1545">1545</biblScope>
<biblScope unit="page" to="1555">1555</biblScope>
</imprint>
<idno type="ISSN">0964-6906</idno>
</series>
<idno type="istex">B9ADA09039B1D374381A8FA829BEC4470EE6605F</idno>
<idno type="DOI">10.1093/hmg/ddp046</idno>
<idno type="ArticleID">ddp046</idno>
</biblStruct>
</sourceDesc>
<seriesStmt>
<idno type="ISSN">0964-6906</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass></textClass>
<langUsage>
<language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front>
<div type="abstract">Germline CDH1 point or small frameshift mutations can be identified in 3050 of hereditary diffuse gastric cancer (HDGC) families. We hypothesized that CDH1 genomic rearrangements would be found in HDGC and identified 160 families with either two gastric cancers in first-degree relatives and with at least one diffuse gastric cancer (DGC) diagnosed before age 50, or three or more DGC in close relatives diagnosed at any age. Sixty-seven carried germline CDH1 point or small frameshift mutations. We screened germline DNA from the 93 mutation negative probands for large genomic rearrangements by Multiplex Ligation-Dependent Probe Amplification. Potential deletions were validated by RTPCR and breakpoints cloned using a combination of oligo-CGH-arrays and long-range-PCR. In-silico analysis of the CDH1 locus was used to determine a potential mechanism for these rearrangements. Six of 93 (6.5) previously described mutation negative HDGC probands, from low GC incidence populations (UK and North America), carried genomic deletions (UK and North America). Two families carried an identical deletion spanning 193 593 bp, encompassing the full CDH3 sequence and CDH1 exons 1 and 2. Other deletions affecting exons 1, 2, 15 and/or 16 were identified. The statistically significant over-representation of Alus around breakpoints indicates it as a likely mechanism for these deletions. When all mutations and deletions are considered, the overall frequency of CDH1 alterations in HDGC is 46 (73/160). CDH1 large deletions occur in 4 of HDGC families by mechanisms involving mainly non-allelic homologous recombination in Alu repeat sequences. As the finding of pathogenic CDH1 mutations is useful for management of HDGC families, screening for deletions should be offered to at-risk families.</div>
</front>
</TEI>
</record>

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