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Title:
Genome remodelling in a basal-like breast cancer metastasis and xenograft | Nature
Description:
Massively parallel DNA sequencing technologies provide an unprecedented ability to screen entire genomes for genetic changes associated with tumour progression. Here we describe the genomic analyses of four DNA samples from an African-American patient with basal-like breast cancer: peripheral blood, the primary tumour, a brain metastasis and a xenograft derived from the primary tumour. The metastasis contained two de novo mutations and a large deletion not present in the primary tumour, and was significantly enriched for 20 shared mutations. The xenograft retained all primary tumour mutations and displayed a mutation enrichment pattern that resembled the metastasis. Two overlapping large deletions, encompassing CTNNA1, were present in all three tumour samples. The differential mutation frequencies and structural variation patterns in metastasis and xenograft compared with the primary tumour indicate that secondary tumours may arise from a minority of cells within the primary tumour. With the latest DNA sequencing technologies it is now possible to screen an entire genome for the genetic changes associated with tumour progression. This approach has been used to obtain complete sequences of four DNA samples from a 44-year-old African-American patient with basal-like breast cancer: the primary tumour, peripheral blood, a brain metastasis and a first-passage xenograft derived from the primary tumour. Mutational analysis suggests that the metastasis tumour specifically selects a subset of cells from the primary tumour that contain pre-existing mutations, and also develops a small number of de novo mutations. Massively parallel DNA sequencing allows entire genomes to be screened for genetic changes associated with tumour progression. Here, the genomes of four DNA samples from a 44-year-old African-American patient with basal-like breast cancer were analysed. The samples came from peripheral blood, the primary tumour, a brain metastasis and a xenograft derived from the primary tumour. The findings indicate that cells with a distinct subset of the primary tumour mutation might be selected during metastasis and xenografting.
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headline:Genome remodelling in a basal-like breast cancer metastasis and xenograft
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headline:Genome remodelling in a basal-like breast cancer metastasis and xenograft
description:Massively parallel DNA sequencing technologies provide an unprecedented ability to screen entire genomes for genetic changes associated with tumour progression. Here we describe the genomic analyses of four DNA samples from an African-American patient with basal-like breast cancer: peripheral blood, the primary tumour, a brain metastasis and a xenograft derived from the primary tumour. The metastasis contained two de novo mutations and a large deletion not present in the primary tumour, and was significantly enriched for 20 shared mutations. The xenograft retained all primary tumour mutations and displayed a mutation enrichment pattern that resembled the metastasis. Two overlapping large deletions, encompassing CTNNA1, were present in all three tumour samples. The differential mutation frequencies and structural variation patterns in metastasis and xenograft compared with the primary tumour indicate that secondary tumours may arise from a minority of cells within the primary tumour. With the latest DNA sequencing technologies it is now possible to screen an entire genome for the genetic changes associated with tumour progression. This approach has been used to obtain complete sequences of four DNA samples from a 44-year-old African-American patient with basal-like breast cancer: the primary tumour, peripheral blood, a brain metastasis and a first-passage xenograft derived from the primary tumour. Mutational analysis suggests that the metastasis tumour specifically selects a subset of cells from the primary tumour that contain pre-existing mutations, and also develops a small number of de novo mutations. Massively parallel DNA sequencing allows entire genomes to be screened for genetic changes associated with tumour progression. Here, the genomes of four DNA samples from a 44-year-old African-American patient with basal-like breast cancer were analysed. The samples came from peripheral blood, the primary tumour, a brain metastasis and a xenograft derived from the primary tumour. The findings indicate that cells with a distinct subset of the primary tumour mutation might be selected during metastasis and xenografting.
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address:
name:The Genome Center at Washington University,,
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name:Michael C. Wendl
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address:
name:The Genome Center at Washington University,,
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name:Department of Genetics,
address:
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name:Joshua F. McMichael
affiliation:
name:The Genome Center at Washington University,
address:
name:The Genome Center at Washington University,,
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name:Vincent J. Magrini
affiliation:
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address:
name:The Genome Center at Washington University,,
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type:Organization
name:Department of Genetics,
address:
name:Department of Genetics,,
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name:Lisa Cook
affiliation:
name:The Genome Center at Washington University,
address:
name:The Genome Center at Washington University,,
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name:Sean D. McGrath
affiliation:
name:The Genome Center at Washington University,
address:
name:The Genome Center at Washington University,,
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name:Tammi L. Vickery
affiliation:
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address:
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affiliation:
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address:
name:The Genome Center at Washington University,,
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name:Katherine DeSchryver
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address:
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address:
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affiliation:
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address:
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type:PostalAddress
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name:Robert Crowder
affiliation:
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address:
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name:Jacqueline E. Snider
affiliation:
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address:
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name:The Genome Center at Washington University,
address:
name:The Genome Center at Washington University,,
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name:Adam F. Dukes
affiliation:
name:The Genome Center at Washington University,
address:
name:The Genome Center at Washington University,,
type:PostalAddress
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name:Gabriel E. Sanderson
affiliation:
name:The Genome Center at Washington University,
address:
name:The Genome Center at Washington University,,
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address:
name:The Genome Center at Washington University,,
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affiliation:
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name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
name:Department of Genetics,,
name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
name:Department of Genetics,,
name:The Genome Center at Washington University,,
name:Department of Genetics,,
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name:Department of Genetics,,
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name:The Genome Center at Washington University,,
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name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
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name:Department of Genetics,,
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name:The Genome Center at Washington University,,
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name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
name:The Genome Center at Washington University,,
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name:Department of Surgery and the Young Womenâs Breast Cancer Program,,
name:Department of Surgery and the Young Womenâs Breast Cancer Program,,
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