Literature DB >> 26995547

Overview of Genetically Engineered Mouse Models of Distinct Breast Cancer Subtypes.

Jerry Usary1, David Brian Darr1, Adam D Pfefferle1, Charles M Perou1.   

Abstract

Advances in the screening of new therapeutic options have significantly reduced the breast cancer death rate over the last decade. Despite these advances, breast cancer remains the second leading cause of cancer death among women. This is due in part to the complexity of the disease, which is characterized by multiple subtypes that are driven by different genetic mechanisms and that likely arise from different cell types of origin. Because these differences often drive treatment options and outcomes, it is important to select relevant preclinical model systems to study new therapeutic interventions and tumor biology. Described in this unit are the characteristics and applications of validated genetically engineered mouse models (GEMMs) of basal-like, luminal, and claudin-low human subtypes of breast cancer. These different subtypes have different clinical outcomes and require different treatment strategies. These GEMMs can be considered faithful surrogates of their human disease counterparts. They represent alternative preclinical tumor models to cell line and patient-derived xenografts for preclinical drug discovery and tumor biology studies.
Copyright © 2016 John Wiley & Sons, Inc.

Entities:  

Keywords:  breast cancer; drug testing; efficacy prediction; gene expression; mouse models

Mesh:

Substances:

Year:  2016        PMID: 26995547      PMCID: PMC4826719          DOI: 10.1002/0471141755.ph1438s72

Source DB:  PubMed          Journal:  Curr Protoc Pharmacol        ISSN: 1934-8282


  42 in total

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Journal:  Chem Biol       Date:  2014-12-11

Review 6.  Molecular characterization of basal-like and non-basal-like triple-negative breast cancer.

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Journal:  Cell       Date:  2012-04-13       Impact factor: 41.582

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Authors:  Melissa A Troester; Jason I Herschkowitz; Daniel S Oh; Xiaping He; Katherine A Hoadley; Claire S Barbier; Charles M Perou
Journal:  BMC Cancer       Date:  2006-12-06       Impact factor: 4.430

9.  Identification of conserved gene expression features between murine mammary carcinoma models and human breast tumors.

Authors:  Jason I Herschkowitz; Karl Simin; Victor J Weigman; Igor Mikaelian; Jerry Usary; Zhiyuan Hu; Karen E Rasmussen; Laundette P Jones; Shahin Assefnia; Subhashini Chandrasekharan; Michael G Backlund; Yuzhi Yin; Andrey I Khramtsov; Roy Bastein; John Quackenbush; Robert I Glazer; Powel H Brown; Jeffrey E Green; Levy Kopelovich; Priscilla A Furth; Juan P Palazzo; Olufunmilayo I Olopade; Philip S Bernard; Gary A Churchill; Terry Van Dyke; Charles M Perou
Journal:  Genome Biol       Date:  2007       Impact factor: 13.583

10.  A comparison of gene expression signatures from breast tumors and breast tissue derived cell lines.

Authors:  D T Ross; C M Perou
Journal:  Dis Markers       Date:  2001       Impact factor: 3.434

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2.  Treg depletion potentiates checkpoint inhibition in claudin-low breast cancer.

Authors:  Nicholas A Taylor; Sarah C Vick; Michael D Iglesia; W June Brickey; Bentley R Midkiff; Karen P McKinnon; Shannon Reisdorf; Carey K Anders; Lisa A Carey; Joel S Parker; Charles M Perou; Benjamin G Vincent; Jonathan S Serody
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3.  FGFR4 regulates tumor subtype differentiation in luminal breast cancer and metastatic disease.

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6.  The AKT1E17K Allele Promotes Breast Cancer in Mice.

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Review 7.  Laboratory Models for Investigating Breast Cancer Therapy Resistance and Metastasis.

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8.  Minibeam radiation therapy enhanced tumor delivery of PEGylated liposomal doxorubicin in a triple-negative breast cancer mouse model.

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