Sequence variants and haplotype analysis of cat ERBB2 gene: a survey on spontaneous cat mammary neoplastic and non-neoplastic lesions
The human ERBB2 proto-oncogene is widely considered a key gene involved in human breast cancer onset and progression. Among spontaneous tumors, mammary tumors are the most frequent cause of cancer death in cats and second most frequent in humans. In fact, naturally occurring tumors in domestic anima...
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Published in: | International journal of molecular sciences Vol. 13; no. 3; pp. 2783 - 2800 |
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Abstract | The human ERBB2 proto-oncogene is widely considered a key gene involved in human breast cancer onset and progression. Among spontaneous tumors, mammary tumors are the most frequent cause of cancer death in cats and second most frequent in humans. In fact, naturally occurring tumors in domestic animals, more particularly cat mammary tumors, have been proposed as a good model for human breast cancer, but critical genetic and molecular information is still scarce. The aims of this study include the analysis of the cat ERBB2 gene partial sequences (between exon 17 and 20) in order to characterize a normal and a mammary lesion heterogeneous populations. Cat genomic DNA was extracted from normal frozen samples (n = 16) and from frozen and formalin-fixed paraffin-embedded mammary lesion samples (n = 41). We amplified and sequenced two cat ERBB2 DNA fragments comprising exons 17 to 20. It was possible to identify five sequence variants and six haplotypes in the total population. Two sequence variants and two haplotypes show to be specific for cat mammary tumor samples. Bioinformatics analysis predicts that four of the sequence variants can produce alternative transcripts or activate cryptic splicing sites. Also, a possible association was identified between clinicopathological traits and the variant haplotypes. As far as we know, this is the first attempt to examine ERBB2 genetic variations in cat mammary genome and its possible association with the onset and progression of cat mammary tumors. The demonstration of a possible association between primary tumor size (one of the two most important prognostic factors) and the number of masses with the cat ERBB2 variant haplotypes reveal the importance of the analysis of this gene in veterinary medicine. |
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AbstractList | The human
ERBB2
proto-oncogene is widely considered a key gene involved in human breast cancer onset and progression. Among spontaneous tumors, mammary tumors are the most frequent cause of cancer death in cats and second most frequent in humans. In fact, naturally occurring tumors in domestic animals, more particularly cat mammary tumors, have been proposed as a good model for human breast cancer, but critical genetic and molecular information is still scarce. The aims of this study include the analysis of the cat
ERBB2
gene partial sequences (between exon 17 and 20) in order to characterize a normal and a mammary lesion heterogeneous populations. Cat genomic DNA was extracted from normal frozen samples (
n
= 16) and from frozen and formalin-fixed paraffin-embedded mammary lesion samples (
n
= 41). We amplified and sequenced two cat
ERBB2
DNA fragments comprising exons 17 to 20. It was possible to identify five sequence variants and six haplotypes in the total population. Two sequence variants and two haplotypes show to be specific for cat mammary tumor samples. Bioinformatics analysis predicts that four of the sequence variants can produce alternative transcripts or activate cryptic splicing sites. Also, a possible association was identified between clinicopathological traits and the variant haplotypes. As far as we know, this is the first attempt to examine
ERBB2
genetic variations in cat mammary genome and its possible association with the onset and progression of cat mammary tumors. The demonstration of a possible association between primary tumor size (one of the two most important prognostic factors) and the number of masses with the cat
ERBB2
variant haplotypes reveal the importance of the analysis of this gene in veterinary medicine. The human ERBB2 proto-oncogene is widely considered a key gene involved in human breast cancer onset and progression. Among spontaneous tumors, mammary tumors are the most frequent cause of cancer death in cats and second most frequent in humans. In fact, naturally occurring tumors in domestic animals, more particularly cat mammary tumors, have been proposed as a good model for human breast cancer, but critical genetic and molecular information is still scarce. The aims of this study include the analysis of the cat ERBB2 gene partial sequences (between exon 17 and 20) in order to characterize a normal and a mammary lesion heterogeneous populations. Cat genomic DNA was extracted from normal frozen samples (n = 16) and from frozen and formalin-fixed paraffin-embedded mammary lesion samples (n = 41). We amplified and sequenced two cat ERBB2 DNA fragments comprising exons 17 to 20. It was possible to identify five sequence variants and six haplotypes in the total population. Two sequence variants and two haplotypes show to be specific for cat mammary tumor samples. Bioinformatics analysis predicts that four of the sequence variants can produce alternative transcripts or activate cryptic splicing sites. Also, a possible association was identified between clinicopathological traits and the variant haplotypes. As far as we know, this is the first attempt to examine ERBB2 genetic variations in cat mammary genome and its possible association with the onset and progression of cat mammary tumors. The demonstration of a possible association between primary tumor size (one of the two most important prognostic factors) and the number of masses with the cat ERBB2 variant haplotypes reveal the importance of the analysis of this gene in veterinary medicine. |
Author | Baptista, Cláudia S Caloustian, Christophe Guedes-Pinto, Henrique Santos, Sara Bastos, Estela Sá, Daniela Gut, Ivo G Chaves, Raquel Gärtner, Fátima |
AuthorAffiliation | 6 Institute of Pathology and Immunology of the University of Porto (IPATIMUP), Rua Dr. Roberto Frias, s/n, 4200-465 Porto, Portugal; E-Mail: fgartner@ipatimup.pt 4 CEA/DSV/IG-Centre National de Génotypage, Bâtiment G2, 2 rue Gaston Crémieux, CP 5721, 91057 Evry Cedex, France; E-Mails: igut@pcb.ub.es (I.G.G.); caloust@cng.fr (C.C.) 1 Institute for Biotechnology and Bioengineering, Centre of Genomics and Biotechnology, University of Trás-os-Montes and Alto Douro (IBB, CGB-UTAD), Quinta de Prados, 5001-801 Vila Real, Portugal; E-Mails: sarasantos@utad.pt (S.S.); ebastos@utad.pt (E.B.); danielasa@portugalmail.com (D.S.); hgp@utad.pt (H.G.-P.) 2 Department of Genetics and Biotechnology, University of Trás-os-Montes and Alto Douro, Quinta de Prados, 5001-801 Vila Real, Portugal 3 Department of Veterinary Clinics, Institute of Biomedical Sciences Abel Salazar, University of Porto (ICBAS-UP), Largo Professor Abel Salazar, 2, 4099-003 Porto, Portugal; E-Mail: csbaptista@icbas.up.pt 5 Department of P |
AuthorAffiliation_xml | – name: 1 Institute for Biotechnology and Bioengineering, Centre of Genomics and Biotechnology, University of Trás-os-Montes and Alto Douro (IBB, CGB-UTAD), Quinta de Prados, 5001-801 Vila Real, Portugal; E-Mails: sarasantos@utad.pt (S.S.); ebastos@utad.pt (E.B.); danielasa@portugalmail.com (D.S.); hgp@utad.pt (H.G.-P.) – name: 2 Department of Genetics and Biotechnology, University of Trás-os-Montes and Alto Douro, Quinta de Prados, 5001-801 Vila Real, Portugal – name: 3 Department of Veterinary Clinics, Institute of Biomedical Sciences Abel Salazar, University of Porto (ICBAS-UP), Largo Professor Abel Salazar, 2, 4099-003 Porto, Portugal; E-Mail: csbaptista@icbas.up.pt – name: 5 Department of Pathology and Molecular Immunology, Institute of Biomedical Sciences Abel Salazar (ICBAS), University of Porto, Largo Prof. Abel Salazar 2, 4099-003 Porto, Portugal – name: 6 Institute of Pathology and Immunology of the University of Porto (IPATIMUP), Rua Dr. Roberto Frias, s/n, 4200-465 Porto, Portugal; E-Mail: fgartner@ipatimup.pt – name: 4 CEA/DSV/IG-Centre National de Génotypage, Bâtiment G2, 2 rue Gaston Crémieux, CP 5721, 91057 Evry Cedex, France; E-Mails: igut@pcb.ub.es (I.G.G.); caloust@cng.fr (C.C.) |
Author_xml | – sequence: 1 givenname: Sara surname: Santos fullname: Santos, Sara email: sarasantos@utad.pt, ebastos@utad.pt, danielasa@portugalmail.com, hgp@utad.pt organization: Institute for Biotechnology and Bioengineering, Centre of Genomics and Biotechnology, University of Trás-os-Montes and Alto Douro (IBB, CGB-UTAD), Quinta de Prados, 5001-801 Vila Real, Portugal; E-Mails: sarasantos@utad.pt (S.S.); ebastos@utad.pt (E.B.); danielasa@portugalmail.com (D.S.); hgp@utad.pt (H.G.-P.) – sequence: 2 givenname: Estela surname: Bastos fullname: Bastos, Estela – sequence: 3 givenname: Cláudia S surname: Baptista fullname: Baptista, Cláudia S – sequence: 4 givenname: Daniela surname: Sá fullname: Sá, Daniela – sequence: 5 givenname: Christophe surname: Caloustian fullname: Caloustian, Christophe – sequence: 6 givenname: Henrique surname: Guedes-Pinto fullname: Guedes-Pinto, Henrique – sequence: 7 givenname: Fátima surname: Gärtner fullname: Gärtner, Fátima – sequence: 8 givenname: Ivo G surname: Gut fullname: Gut, Ivo G – sequence: 9 givenname: Raquel surname: Chaves fullname: Chaves, Raquel |
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CitedBy_id | crossref_primary_10_3390_pharmaceutics13030346 crossref_primary_10_3390_vetsci3030017 crossref_primary_10_1017_S1431927613001529 crossref_primary_10_18632_oncotarget_7551 crossref_primary_10_3390_cancers15020384 crossref_primary_10_3390_vetsci2030111 crossref_primary_10_3390_vetsci8080164 crossref_primary_10_1016_j_cyto_2016_05_018 crossref_primary_10_1016_j_rvsc_2017_07_035 crossref_primary_10_3390_ani13193059 crossref_primary_10_1371_journal_pone_0083673 crossref_primary_10_3389_fonc_2022_959630 |
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Keywords | Haplotypes Cat Mammary Tumors (CMT) v-erb-b2 erythroblastic leukemia viral oncogene homolog 2 (ERBB2) Splicing Sites (SS) Sequence Variants (SVs) |
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Snippet | The human ERBB2 proto-oncogene is widely considered a key gene involved in human breast cancer onset and progression. Among spontaneous tumors, mammary tumors... The human ERBB2 proto-oncogene is widely considered a key gene involved in human breast cancer onset and progression. Among spontaneous tumors, mammary tumors... |
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SubjectTerms | Alternative Splicing - genetics Animals Base Sequence Bioinformatics Biotechnology Breast cancer Cat Mammary Tumors (CMT) Cats Cell division DNA Domestic animals Electronic mail systems ErbB-2 protein Exons Female Gene amplification Genes, erbB-2 Genomes genomics Genotype Haplotypes Haplotypes - genetics Histopathology Humans Immunology Kinases Leukemia Lymphatic system Mammary gland Mammary Neoplasms, Animal - genetics Mammary Neoplasms, Animal - pathology Medical prognosis Metastasis Molecular modelling Molecular Sequence Data Mutation Nucleotide sequence Proteins Proto-oncogenes Receptor, ErbB-2 - genetics Sequence Analysis, DNA Sequence Variants (SVs) Splicing Splicing Sites (SS) Tumors v-erb-b2 erythroblastic leukemia viral oncogene homolog 2 (ERBB2) Veterinary medicine |
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Title | Sequence variants and haplotype analysis of cat ERBB2 gene: a survey on spontaneous cat mammary neoplastic and non-neoplastic lesions |
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