Expression Pathology is developing targeted, quantitative mass spectrometry-based assays that can be used to measure protein expression in standard formalin-fixed paraffin-embedded (FFPE) tumor samples. The assays include a wide range of drug target pathway proteins including EFGR, IGF-1R, cMET, cSRC, mTOR, MEK, and ERK, and their phosphorylation states.
Our
assays can be multiplexed and have great potential in drug development, clinical
trials and personalized medicine. Measuring protein expression
in standard
formalin-fixed tissue samples can provide diagnostic
and prognostic information to guide treatment decisions.
Click on image for more details regarding the work flow.
Measure
Multiple Reaction Monitoring (MRM) is an established method for
quantitation of proteins using mass spectrometry. Liquid Tissue® preparations
can be used together with MRM for absolute quantitation of
specific protein biomarkers in FFPE tissue. This is the
foundation for our current development of tests to determine
the expression
of key proteins in for example cell signaling pathways and
druggable targets. Multi-plexed MRM assays can be used to measure many different proteins at the same time.
Recent collaborations involve measurement of Her2 in breast
cancer by labeled peptides, lung cancer biomarkers by MRM and papillomavirus in HIV patients
by iTRAQ. A case study using Her2
expression in invasive breast cancer is available.
Discover and Validate
Our technology can also be used to mine archival tissue
collections for differentially expressed protein biomarkers
in archival tissue collection.
* Companion diagnostics * Prognostic biomarkers
* Drug targets
Modern, high-resolution mass spectrometry is extremely sensitive.
Using only very small amounts of precious patient samples
we do global protein expression screens which profile
the expression of thousands of proteins from patients. Using
our bioinformatics expertise we can identify proteins that
are up or down regulated.
Technology
platform
The patented Liquid
Tissue® MS
reagents extract proteins from FFPE tissue samples and prepares
them for mass spec analysis. The process provides complete
solubilization and captures the entire protein content in
a mass spec friendly format and requires only 30,000 cells.
An integral part of our research it is also
available as a research product for use in your laboratory.
Laser
microdissection is essential for high-quality data in proteomic
and genomic work. DIRECTOR® laser
microdissection use indirect photon biomaterial interactions.
It is covered by two issued patents, and dramatically
improves the
speed, precision and
automatability of tissue microdissection. The DIRECTOR
slides are fully compatible with the three leading laser microdissection
platforms on the market; the Leica
LMD6000, the P.A.L.M.
Microbeam from Zeiss, and the new generation mmi
CellCut Plus from
Molecular Machines & Industries.
Liquid Tissue technology is protected by U.S. Patent 7,473,532
and patents pending and foreign equivalents thereof.
DIRECTOR technology is protected by U.S. Patents 7,294,367
and 7,381,440 and foreign equivalents thereof.
We can support both your R&D needs and work with you to validate our assays for use as companion diagnostics. Our unique blend of expertise in tissue analysis, proteomics,
mass spectrometry and bioinformatics makes us a very
strong collaborator.
Contact us to discuss your tissue proteomic assay and discovery
needs.
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News & Events
Expression Pathology Collaborates with Toronto’s Sick Kids Hospital and University Health Network on New Mass Spec EGFR Test, May 4, 2010, (press release)
Thermo
Fisher announced a collaboration with Expression Pathology to develop
Liquid Tissue MRM Assays of Cancer Proteins In Microdissected FFPE Tissue,
December 16, 2009 (press
release)
The Mayo
Clinic has licensed non-exclusive rights to the Liquid Tissue(R) patent
for use in diagnosis of systemic amyloidosis in FFPE tissue, November 17, 2009 (press
release)
Expression
Pathology raises $6.5 Million
to develop personalized medicine assays for protein biomarkers in FFPE
Tissue. April 20, 2009 (press
release)