alexa Genomic Profiling of Pre-Clinical Models of Inflammatory Breast Cancer Identifies a Signature of Epithelial Plasticity and Suppression of TGFβ Signaling
ISSN: 2161-0681

Journal of Clinical & Experimental Pathology
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Research Article

Genomic Profiling of Pre-Clinical Models of Inflammatory Breast Cancer Identifies a Signature of Epithelial Plasticity and Suppression of TGFβ Signaling

Fredika M Robertson1*, Khoi Chu1, Sandra V Fernandez2, Zhaomei Mu2, Xuejun Zhang1, Hui Liu1, Kimberly M Boley1, R Katherine Alpaugh3, Zaiming Ye1, Moishia C Wright1, Annie Z Luo1, Ricardo oraes1, Hong Wu4, Matthew Zook5, Sanford H Barsky6, Savitri Krishnamurthy7 and Massimo Cristofanilli8

1Department of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA

2Breast Cancer Research Laboratory, Fox Chase Cancer Center, Philadelphia, PA-19111, USA

3Protocol Support Laboratory, Fox Chase Cancer Center, Philadelphia, PA-19111, USA

4Department of Pathology, Fox Chase Cancer Center, Philadelphia, PA-19111, USA

5Department of Medicine, Fox Chase Cancer Center, Philadelphia, PA-19111, USA

6Department of Pathology, The University of Nevada School of Medicine, Reno NV-89557, USA

7Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX-77030, USA

8Department of Medical Oncology, Fox Chase Cancer Center, Philadelphia, PA-19111, USA

*Corresponding Author:
Dr. Fredika M Robertson
Department of Experimental Therapeutics
The University of Texas MD Anderson Cancer Center
Houston, TX-77030, USA
E-mail: [email protected]

Received date: June 26, 2012; Accepted date: July 26, 2012; Published date: July 28, 2012

Citation: Robertson FM, Chu K, Fernandez SV, Mu Z, Zhang X, et al. (2012) Genomic Profiling of Pre-Clinical Models of Inflammatory Breast Cancer Identifies a Signature of Epithelial Plasticity and Suppression of TGFß Signaling. J Clin Exp Pathol 2:119. doi:10.4172/2161-0681.1000119

Copyright: © 2012 Robertson FM, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

Abstract
Study background: Inflammatory Breast Cancer (IBC) is the most metastatic variant of breast cancer. Although
IBC is recognized as a distinct variant of breast cancer, the molecular basis for the rapid progression of IBC remains
largely undefined, in part due to the lack of preclinical models that recapitulate the human disease as well as a lack of
comprehensive analysis of the preclinical models of IBC that are available.
Methods: All available 7 pre-clinical models of IBC, including 2 new models, FC-IBC01 and FC-IBC02 developed
from pleural effusion, were used to identify genes and molecular pathways that are selectively altered compared to non
IBC breast tumor models. Laser capture micro dissection of biopsy tissue from core biopsy and skin punch biopsies
were also analyzed by whole transcriptome analysis.
Results: Whole transcriptome analysis defined 7 pre-clinical models of IBC as being within either the triple
negative or ErbB2/Her-2 expressing subtypes, similar to the prevalence of these subtypes of breast cancer observed
in IBC patients. Comparative analysis of the FC-IBC01, FC-IBC02 and Mary-X models of IBC demonstrated that each
of these recapitulate the formation of tumor emboli with encircling lymphovasculogenesis. The majority (6/7) of the
pre-clinical models of IBC express CDH1, which encodes for E-cadherin, which was associated with a loss of ZEB1,
a transcriptional repressor of E-cadherin.
The lack of ZEB1 expression was validated in a limited set of 4 skin punch biopsy samples from IBC patients that
were isolated by laser capture micro-dissection, demonstrating concordance with loss of ZEB1 in pre-clinical models of
IBC. Expression of other transcription factors involved in acquisition of a cancer stem cell phenotype, including Snai1,
which encodes for Snail, SNAI2, which encodes for Slug and TWIST1, was retained in pre-clinical models of IBC.
Maintenance of E-cadherin in pre-clinical models of IBC was associated with a loss of genes within the transforming
growth factor beta (TGFβ signaling pathway, with expression of SMAD6, a known repressor of TGFβ. This is similar
to a recent study reporting the persistence of E-cadherin and loss of TGFβ signaling in IBC patient tumors based on
gene profiling of 3 independent data sets.
Conclusion: The present studies provide first time comparison of gene signatures of 7 pre-clinical models of IBC,
including our 2 newly developed pre-clinical models, FC-IBC01 and FC-IBC02, that recapitulate formation of tumor
emboli with encircling lymphatic vessels, similar to that observed in biopsy tissues of IBC patients. We demonstrate
that E-cadherin expression was associated with both loss of ZEB1 and diminished expression of multiple genes within
the TGFβ signaling pathway, with retention of expression of transcription factors and surface markers consistent with
maintenance of a cancer stem cell phenotype, as has been reported to be a characteristic of IBC tumors. Collectively,
these observations provide first time characterization of the molecular signatures of all available pre-clinical models
of IBC, and suggest that IBC has a signature of epithelial plasticity, with characteristics of their ability to undergo the
mesenchymal to epithelial reverting transition. The loss of genes within the TGFβ signaling is also consistent with the
tight cell: cell aggregation of IBC tumor cells within tumor emboli that exhibit “cohesive invasion”. The new pre-clinical
models of IBC that recapitulate the human disease will serve as useful tools to accelerate our understanding of the
molecular underpinnings and therapeutic targets of IBC as the most lethal form of breast cancer.

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