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Multiplexed cell signaling analysis of human breast cancer applications for personalized therapy.
- Source :
-
Journal of proteome research [J Proteome Res] 2008 Apr; Vol. 7 (4), pp. 1508-17. Date of Electronic Publication: 2008 Feb 08. - Publication Year :
- 2008
-
Abstract
- Phosphoprotein driven cellular signaling events represent most of the new molecular targets for cancer treatment. Application of reverse-phase protein microarray technology for the study of ongoing signaling activity within breast tumor specimens holds great potential for elucidating and profiling signaling activity in real-time for patient-tailored therapy. Analysis of laser capture microdissection primary human breast tumors and metastatic lesions reveals pathway specific profiles and a new way to classify cancer based on functional signaling portraits. Moreover, the data demonstrate the requirement of laser capture microdissection for analysis and reveal the metastasis-specific changes that occur within a new microenvironment. Analysis of biopsy material from clinical trials for targeted therapeutics demonstrates the feasibility and utility of comprehensive signal pathway activation profiling for molecular analysis.
- Subjects :
- Breast Neoplasms drug therapy
Breast Neoplasms pathology
Cluster Analysis
Erlotinib Hydrochloride
Female
Humans
Lasers
Liver Neoplasms drug therapy
Liver Neoplasms metabolism
Liver Neoplasms secondary
Microdissection methods
Phosphoproteins metabolism
Phosphorylation
Protein Kinase Inhibitors therapeutic use
Protein Kinases metabolism
Proto-Oncogene Proteins c-akt metabolism
Quinazolines therapeutic use
Receptor Protein-Tyrosine Kinases metabolism
Breast Neoplasms metabolism
Intracellular Signaling Peptides and Proteins metabolism
Proteomics methods
Signal Transduction
Subjects
Details
- Language :
- English
- ISSN :
- 1535-3893
- Volume :
- 7
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Journal of proteome research
- Publication Type :
- Academic Journal
- Accession number :
- 18257519
- Full Text :
- https://doi.org/10.1021/pr7008127