Common Fragile Site Tumor Suppressor Genes and Corresponding Mouse Models of Cancer
Chromosomal common fragile sites (CFSs) are specific mammalian genomic regions that show an increased frequency of gaps and breaks when cells are exposed to replication stress in vitro. CFSs are also consistently involved in chromosomal abnormalities in vivo related to cancer. Interestingly, several...
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doaj-8855851d670e431aa0faaaf45fa4b0912020-11-25T00:25:27ZengHindawi LimitedJournal of Biomedicine and Biotechnology1110-72431110-72512011-01-01201110.1155/2011/984505984505Common Fragile Site Tumor Suppressor Genes and Corresponding Mouse Models of CancerAlessandra Drusco0Yuri Pekarsky1Stefan Costinean2Anna Antenucci3Laura Conti4Stefano Volinia5Rami I. Aqeilan6Kay Huebner7Nicola Zanesi8Department of Molecular Virology, Immunology, and Medical Genetics, The Ohio State University, Columbus, OH 43210 , USADepartment of Molecular Virology, Immunology, and Medical Genetics, The Ohio State University, Columbus, OH 43210 , USADepartment of Molecular Virology, Immunology, and Medical Genetics, The Ohio State University, Columbus, OH 43210 , USAClinical Pathology, Regina Elena Institute, IFO, 00144 Rome, ItalyClinical Pathology, Regina Elena Institute, IFO, 00144 Rome, ItalyDepartment of Molecular Virology, Immunology, and Medical Genetics, The Ohio State University, Columbus, OH 43210 , USADepartment of Molecular Virology, Immunology, and Medical Genetics, The Ohio State University, Columbus, OH 43210 , USADepartment of Molecular Virology, Immunology, and Medical Genetics, The Ohio State University, Columbus, OH 43210 , USADepartment of Molecular Virology, Immunology, and Medical Genetics, The Ohio State University, Columbus, OH 43210 , USAChromosomal common fragile sites (CFSs) are specific mammalian genomic regions that show an increased frequency of gaps and breaks when cells are exposed to replication stress in vitro. CFSs are also consistently involved in chromosomal abnormalities in vivo related to cancer. Interestingly, several CFSs contain one or more tumor suppressor genes whose structure and function are often affected by chromosomal fragility. The two most active fragile sites in the human genome are FRA3B and FRA16D where the tumor suppressor genes FHIT and WWOX are located, respectively. The best approach to study tumorigenic effects of altered tumor suppressors located at CFSs in vivo is to generate mouse models in which these genes are inactivated. This paper summarizes our present knowledge on mouse models of cancer generated by knocking out tumor suppressors of CFS.http://dx.doi.org/10.1155/2011/984505 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Alessandra Drusco Yuri Pekarsky Stefan Costinean Anna Antenucci Laura Conti Stefano Volinia Rami I. Aqeilan Kay Huebner Nicola Zanesi |
spellingShingle |
Alessandra Drusco Yuri Pekarsky Stefan Costinean Anna Antenucci Laura Conti Stefano Volinia Rami I. Aqeilan Kay Huebner Nicola Zanesi Common Fragile Site Tumor Suppressor Genes and Corresponding Mouse Models of Cancer Journal of Biomedicine and Biotechnology |
author_facet |
Alessandra Drusco Yuri Pekarsky Stefan Costinean Anna Antenucci Laura Conti Stefano Volinia Rami I. Aqeilan Kay Huebner Nicola Zanesi |
author_sort |
Alessandra Drusco |
title |
Common Fragile Site Tumor Suppressor Genes and Corresponding Mouse
Models of Cancer |
title_short |
Common Fragile Site Tumor Suppressor Genes and Corresponding Mouse
Models of Cancer |
title_full |
Common Fragile Site Tumor Suppressor Genes and Corresponding Mouse
Models of Cancer |
title_fullStr |
Common Fragile Site Tumor Suppressor Genes and Corresponding Mouse
Models of Cancer |
title_full_unstemmed |
Common Fragile Site Tumor Suppressor Genes and Corresponding Mouse
Models of Cancer |
title_sort |
common fragile site tumor suppressor genes and corresponding mouse
models of cancer |
publisher |
Hindawi Limited |
series |
Journal of Biomedicine and Biotechnology |
issn |
1110-7243 1110-7251 |
publishDate |
2011-01-01 |
description |
Chromosomal common fragile sites (CFSs) are specific mammalian genomic regions that show an increased frequency of gaps and breaks when cells are exposed to replication stress in vitro. CFSs are also consistently involved in chromosomal abnormalities in vivo related to cancer. Interestingly, several CFSs contain one or more tumor suppressor genes whose structure and function are often affected by chromosomal fragility. The two most active fragile sites in the human genome are FRA3B and FRA16D where the tumor suppressor genes FHIT and WWOX are located, respectively. The best approach to study tumorigenic effects of altered tumor suppressors located at CFSs in vivo is to generate mouse models in which these genes are inactivated. This paper summarizes our present knowledge on mouse models of cancer generated by knocking out tumor suppressors of CFS. |
url |
http://dx.doi.org/10.1155/2011/984505 |
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