Targeted biomarker profiling of matched primary and metastatic estrogen receptor positive breast cancers

Patients with newly diagnosed, early stage estrogen receptor positive (ER+) breast cancer often show disease free survival in excess of five years following surgery and systemic adjuvant therapy. An important question is whether diagnostic tumor tissue from the primary lesion offers an accurate mole...

Full description

Saved in:
Bibliographic Details
Published inPloS one Vol. 9; no. 2; p. e88401
Main Authors Schleifman, Erica B, Desai, Rupal, Spoerke, Jill M, Xiao, Yuanyuan, Wong, Cheryl, Abbas, Ilma, O'Brien, Carol, Patel, Rajesh, Sumiyoshi, Teiko, Fu, Ling, Tam, Rachel N, Koeppen, Hartmut, Wilson, Timothy R, Raja, Rajiv, Hampton, Garret M, Lackner, Mark R
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 10.02.2014
Public Library of Science (PLoS)
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Patients with newly diagnosed, early stage estrogen receptor positive (ER+) breast cancer often show disease free survival in excess of five years following surgery and systemic adjuvant therapy. An important question is whether diagnostic tumor tissue from the primary lesion offers an accurate molecular portrait of the cancer post recurrence and thus may be used for predictive diagnostic purposes for patients with relapsed, metastatic disease. As the class I phosphatidylinositol 3' kinase (PI3K) pathway is frequently activated in ER+ breast cancer and has been linked to acquired resistance to hormonal therapy, we hypothesized pathway status could evolve over time and treatment. Biomarker analyses were conducted on matched, asynchronous primary and metastatic tumors from 77 patients with ER+ breast cancer. We examined whether PIK3CA and AKT1 alterations or PTEN and Ki67 levels showed differences between primary and metastatic samples. We also sought to look more broadly at gene expression markers reflective of proliferation, molecular subtype, and key receptors and signaling pathways using an mRNA analysis platform developed on the Fluidigm BioMark™ microfluidics system to measure the relative expression of 90 breast cancer related genes in formalin-fixed paraffin-embedded (FFPE) tissue. Application of this panel of biomarker assays to matched tumor pairs showed a high concordance between primary and metastatic tissue, with generally few changes in mutation status, proliferative markers, or gene expression between matched samples. The collection of assays described here has been optimized for FFPE tissue and may have utility in exploratory analyses to identify patient subsets responsive to targeted therapies.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Competing Interests: All of the authors are current or former employees of Genentech, Inc, and this research was wholly funded by Genentech, Inc. These facts do not alter the authors' adherence to all the PLOS ONE policies on sharing data and materials, and the manuscript does not describe marketed products or products in development by Genentech, Inc. Other than that, none of the authors have conflicts of interest to disclose.
Conceived and designed the experiments: ES RD JS RR TW GH ML. Performed the experiments: ES RD CW IA RT RP HK CO JM. Analyzed the data: YX ES HK RD JS RP RT TS ML. Contributed reagents/materials/analysis tools: ES RD JM YX CW IA CO RP TS LF RT HK. Wrote the paper: ES RD JM ML.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0088401