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Integrated analysis of canine soft tissue sarcomas identifies recurrent mutations in TP53, KMT genes and PDGFB fusions
by
Das, Sunetra
, Regan, Daniel P.
, Idate, Rupa
, Duval, Dawn L.
, Lana, Susan E.
in
631/114
/ 631/67
/ Animals
/ Becaplermin - genetics
/ Cell cycle
/ Chromatin
/ DNA repair
/ Dogs
/ Extracellular matrix
/ Fibrosarcoma
/ Genomics
/ Histiocytoma, Malignant Fibrous
/ Homeobox
/ Humanities and Social Sciences
/ Immunohistochemistry
/ Lymphocytes T
/ Metastases
/ multidisciplinary
/ Mutation
/ p53 Protein
/ Peripheral nerves
/ Pets
/ Platelet-derived growth factor
/ Proto-Oncogene Proteins c-sis - genetics
/ Sarcoma
/ Sarcoma - genetics
/ Sarcoma - pathology
/ Sarcoma - veterinary
/ Science
/ Science (multidisciplinary)
/ Soft Tissue Neoplasms - pathology
/ Transcription factors
/ Transcription Factors - genetics
/ Transcriptomics
/ Tumor Suppressor Protein p53 - genetics
/ Tumors
2023
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Integrated analysis of canine soft tissue sarcomas identifies recurrent mutations in TP53, KMT genes and PDGFB fusions
by
Das, Sunetra
, Regan, Daniel P.
, Idate, Rupa
, Duval, Dawn L.
, Lana, Susan E.
in
631/114
/ 631/67
/ Animals
/ Becaplermin - genetics
/ Cell cycle
/ Chromatin
/ DNA repair
/ Dogs
/ Extracellular matrix
/ Fibrosarcoma
/ Genomics
/ Histiocytoma, Malignant Fibrous
/ Homeobox
/ Humanities and Social Sciences
/ Immunohistochemistry
/ Lymphocytes T
/ Metastases
/ multidisciplinary
/ Mutation
/ p53 Protein
/ Peripheral nerves
/ Pets
/ Platelet-derived growth factor
/ Proto-Oncogene Proteins c-sis - genetics
/ Sarcoma
/ Sarcoma - genetics
/ Sarcoma - pathology
/ Sarcoma - veterinary
/ Science
/ Science (multidisciplinary)
/ Soft Tissue Neoplasms - pathology
/ Transcription factors
/ Transcription Factors - genetics
/ Transcriptomics
/ Tumor Suppressor Protein p53 - genetics
/ Tumors
2023
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Integrated analysis of canine soft tissue sarcomas identifies recurrent mutations in TP53, KMT genes and PDGFB fusions
by
Das, Sunetra
, Regan, Daniel P.
, Idate, Rupa
, Duval, Dawn L.
, Lana, Susan E.
in
631/114
/ 631/67
/ Animals
/ Becaplermin - genetics
/ Cell cycle
/ Chromatin
/ DNA repair
/ Dogs
/ Extracellular matrix
/ Fibrosarcoma
/ Genomics
/ Histiocytoma, Malignant Fibrous
/ Homeobox
/ Humanities and Social Sciences
/ Immunohistochemistry
/ Lymphocytes T
/ Metastases
/ multidisciplinary
/ Mutation
/ p53 Protein
/ Peripheral nerves
/ Pets
/ Platelet-derived growth factor
/ Proto-Oncogene Proteins c-sis - genetics
/ Sarcoma
/ Sarcoma - genetics
/ Sarcoma - pathology
/ Sarcoma - veterinary
/ Science
/ Science (multidisciplinary)
/ Soft Tissue Neoplasms - pathology
/ Transcription factors
/ Transcription Factors - genetics
/ Transcriptomics
/ Tumor Suppressor Protein p53 - genetics
/ Tumors
2023
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Integrated analysis of canine soft tissue sarcomas identifies recurrent mutations in TP53, KMT genes and PDGFB fusions
Journal Article
Integrated analysis of canine soft tissue sarcomas identifies recurrent mutations in TP53, KMT genes and PDGFB fusions
2023
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Overview
Soft tissue sarcomas (STS) are a heterogenous group of mesenchymal tumors representing over 50 distinct types with overlapping histological features and non-specific anatomical locations. Currently, localized sarcomas are treated with surgery + / − radiation in both humans and dogs with few molecularly targeted therapeutic options. However, to improve precision-based cancer therapy through trials in pet dogs with naturally occurring STS tumors, knowledge of genomic profiling and molecular drivers in both species is essential. To this purpose, we sought to characterize the transcriptomic and genomic mutation profiles of canine STS subtypes (fibrosarcoma, undifferentiated pleomorphic sarcoma, and peripheral nerve sheath tumors), by leveraging RNAseq, whole exome sequencing, immunohistochemistry, and drug assays. The most common driver mutations were in cell cycle/DNA repair (31%,
TP53
-21%) and chromatin organization/binding (41%,
KMT2D
-21%) genes. Similar to a subset of human sarcomas, we identified fusion transcripts of platelet derived growth factor B and collagen genes that predict sensitivity to PDGFR inhibitors. Transcriptomic profiling grouped these canine STS tumors into 4 clusters, one PNST group (H1), and 3 FSA groups selectively enriched for extracellular matrix interactions and
PDFGB
fusions (H2), homeobox transcription factors (H3), and elevated T-cell infiltration (H4). This multi-omics approach provides insights into canine STS sub-types at a molecular level for comparison to their human counterparts, to improve diagnosis, and may provide additional targets for chemo- and immuno-therapy.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
/ 631/67
/ Animals
/ Dogs
/ Genomics
/ Histiocytoma, Malignant Fibrous
/ Homeobox
/ Humanities and Social Sciences
/ Mutation
/ Pets
/ Platelet-derived growth factor
/ Proto-Oncogene Proteins c-sis - genetics
/ Sarcoma
/ Science
/ Soft Tissue Neoplasms - pathology
/ Transcription Factors - genetics
/ Tumor Suppressor Protein p53 - genetics
/ Tumors
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