LymphedemaV1, PubMed, Checkpoint, bibRecord, 001113

A novel animal model for locally advanced breast cancer.

Identifieur interne : 001113 ( PubMed/Checkpoint ); précédent : 001112; suivant : 001114

A novel animal model for locally advanced breast cancer.

Auteurs : Maria V. Bogachek [États-Unis] ; Jung Min Park ; James P. De Andrade ; Mikhail V. Kulak ; Jeffrey R. White ; Tong Wu ; Philip M. Spanheimer ; Thomas B. Bair ; Alicia K. Olivier ; Ronald J. Weigel

Source :

Annals of surgical oncology [ 1534-4681 ] ; 2015.

RBID : pubmed:25326397

Descripteurs français

English descriptors

KwdEn :
- Animals, Biomarkers, Tumor (genetics), Biomarkers, Tumor (metabolism), Blotting, Western, Breast Neoplasms (genetics), Breast Neoplasms (metabolism), Breast Neoplasms (pathology), Carcinoma, Ductal, Breast (genetics), Carcinoma, Ductal, Breast (metabolism), Carcinoma, Ductal, Breast (pathology), Cell Proliferation, Disease Models, Animal, Female, Flow Cytometry, Fluorescent Antibody Technique, Gene Expression Profiling, Humans, Mice, Mice, Nude, Oligonucleotide Array Sequence Analysis, RNA, Messenger (genetics), Real-Time Polymerase Chain Reaction, Reverse Transcriptase Polymerase Chain Reaction, Tumor Cells, Cultured, Xenograft Model Antitumor Assays.
MESH :
- chemical , genetics : Biomarkers, Tumor, RNA, Messenger.
- chemical , metabolism : Biomarkers, Tumor.
- genetics : Breast Neoplasms, Carcinoma, Ductal, Breast.
- metabolism : Breast Neoplasms, Carcinoma, Ductal, Breast.
- pathology : Breast Neoplasms, Carcinoma, Ductal, Breast.
- Animals, Blotting, Western, Cell Proliferation, Disease Models, Animal, Female, Flow Cytometry, Fluorescent Antibody Technique, Gene Expression Profiling, Humans, Mice, Mice, Nude, Oligonucleotide Array Sequence Analysis, Real-Time Polymerase Chain Reaction, Reverse Transcriptase Polymerase Chain Reaction, Tumor Cells, Cultured, Xenograft Model Antitumor Assays.

Abstract

Locally advanced breast cancer (LABC) poses complex management issues due to failure of response to chemotherapy and progression to local complications such as skin erosion, superinfection, and lymphedema. Most cell line and animal models are not adequate to study LABC.

DOI: 10.1245/s10434-014-4174-8
PubMed: 25326397

Affiliations:

Links toward previous steps (curation, corpus...)

to stream PubMed, to step Corpus: 001251
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Links to Exploration step

pubmed:25326397

Le document en format XML

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<term>Fluorescent Antibody Technique</term>
<term>Gene Expression Profiling</term>
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<term>Mice</term>
<term>Mice, Nude</term>
<term>Oligonucleotide Array Sequence Analysis</term>
<term>RNA, Messenger (genetics)</term>
<term>Real-Time Polymerase Chain Reaction</term>
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<term>Carcinome canalaire du sein (génétique)</term>
<term>Carcinome canalaire du sein (métabolisme)</term>
<term>Cellules cancéreuses en culture</term>
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<term>Marqueurs biologiques tumoraux (métabolisme)</term>
<term>Modèles animaux de maladie humaine</term>
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<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Breast Neoplasms</term>
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<term>Blotting, Western</term>
<term>Cell Proliferation</term>
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<term>Female</term>
<term>Flow Cytometry</term>
<term>Fluorescent Antibody Technique</term>
<term>Gene Expression Profiling</term>
<term>Humans</term>
<term>Mice</term>
<term>Mice, Nude</term>
<term>Oligonucleotide Array Sequence Analysis</term>
<term>Real-Time Polymerase Chain Reaction</term>
<term>Reverse Transcriptase Polymerase Chain Reaction</term>
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<term>Cellules cancéreuses en culture</term>
<term>Cytométrie en flux</term>
<term>Femelle</term>
<term>Humains</term>
<term>Modèles animaux de maladie humaine</term>
<term>Prolifération cellulaire</term>
<term>RT-PCR</term>
<term>Réaction de polymérisation en chaine en temps réel</term>
<term>Souris</term>
<term>Souris nude</term>
<term>Séquençage par oligonucléotides en batterie</term>
<term>Technique d'immunofluorescence</term>
<term>Technique de Western</term>
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<front><div type="abstract" xml:lang="en">Locally advanced breast cancer (LABC) poses complex management issues due to failure of response to chemotherapy and progression to local complications such as skin erosion, superinfection, and lymphedema. Most cell line and animal models are not adequate to study LABC.</div>
</front>
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<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">25326397</PMID>
<DateCreated><Year>2015</Year>
<Month>02</Month>
<Day>04</Day>
</DateCreated>
<DateCompleted><Year>2015</Year>
<Month>10</Month>
<Day>20</Day>
</DateCompleted>
<DateRevised><Year>2017</Year>
<Month>02</Month>
<Day>20</Day>
</DateRevised>
<Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1534-4681</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>22</Volume>
<Issue>3</Issue>
<PubDate><Year>2015</Year>
<Month>Mar</Month>
</PubDate>
</JournalIssue>
<Title>Annals of surgical oncology</Title>
<ISOAbbreviation>Ann. Surg. Oncol.</ISOAbbreviation>
</Journal>
<ArticleTitle>A novel animal model for locally advanced breast cancer.</ArticleTitle>
<Pagination><MedlinePgn>866-73</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1245/s10434-014-4174-8</ELocationID>
<Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Locally advanced breast cancer (LABC) poses complex management issues due to failure of response to chemotherapy and progression to local complications such as skin erosion, superinfection, and lymphedema. Most cell line and animal models are not adequate to study LABC.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">A patient-derived xenograft (IOWA-1T) from a patient with LABC was characterized for expression profile, short tandem repeat profile, oncogenic mutations, xenograft growth, and response to therapy.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Short tandem repeat profile authenticated the cell line as derived from a human woman. The primary tumor and derived xenografts were weakly estrogen receptor alpha positive (<5%), progesterone receptor negative, and HER2 nonamplified. Expression array profile compared to MCF-7 and BT-549 cell lines indicate that IOWA-1T was more closely related to basal breast cancer. IOWA-1T harbors a homozygous R248Q mutation of the TP53 gene; in vitro invasion assay was comparable to BT-549 and greater than MCF-7. IOWA-1T xenografts developed palpable tumors in 9.6 ± 1.6 days, compared to 49 ± 13 days for parallel experiments with BT-20 cells (p < 0.002). Tumor xenografts became locally advanced, growing to >2 cm in 21.6 ± 2 days, characterized by skin erosion necessitating euthanasia. The SUMO inhibitor anacardic acid inhibited the outgrowth of IOWA-1T xenografts, while doxorubicin had no effect on tumorigenesis.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">IOWA-1T is a novel cell line with an expression pattern consistent with basal breast cancer. Xenografts recapitulated LABC and provide a novel model for testing therapeutic drugs that may be effective in cases resistant to conventional chemotherapy.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Bogachek</LastName>
<ForeName>Maria V</ForeName>
<Initials>MV</Initials>
<AffiliationInfo><Affiliation>Department of Surgery, University of Iowa, Iowa City, IA, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Park</LastName>
<ForeName>Jung Min</ForeName>
<Initials>JM</Initials>
</Author>
<Author ValidYN="Y"><LastName>De Andrade</LastName>
<ForeName>James P</ForeName>
<Initials>JP</Initials>
</Author>
<Author ValidYN="Y"><LastName>Kulak</LastName>
<ForeName>Mikhail V</ForeName>
<Initials>MV</Initials>
</Author>
<Author ValidYN="Y"><LastName>White</LastName>
<ForeName>Jeffrey R</ForeName>
<Initials>JR</Initials>
</Author>
<Author ValidYN="Y"><LastName>Wu</LastName>
<ForeName>Tong</ForeName>
<Initials>T</Initials>
</Author>
<Author ValidYN="Y"><LastName>Spanheimer</LastName>
<ForeName>Philip M</ForeName>
<Initials>PM</Initials>
</Author>
<Author ValidYN="Y"><LastName>Bair</LastName>
<ForeName>Thomas B</ForeName>
<Initials>TB</Initials>
</Author>
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<ForeName>Alicia K</ForeName>
<Initials>AK</Initials>
</Author>
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<ForeName>Ronald J</ForeName>
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<CommentsCorrections RefType="Cites"><RefSource>Br J Cancer. 2014 Mar 18;110(6):1413-9</RefSource>
<PMID Version="1">24569467</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Methods. 2012 Mar;56(3):432-9</RefSource>
<PMID Version="1">22445873</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>J Clin Oncol. 2010 Jun 1;28(16):2784-95</RefSource>
<PMID Version="1">20404251</PMID>
</CommentsCorrections>
</CommentsCorrectionsList>
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A novel animal model for locally advanced breast cancer.

A novel animal model for locally advanced breast cancer.

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