Role of oncoproteomics in the personalized management of cancer
Author: Jain, Kewal K
Source: Expert Review of Proteomics, Volume 1, Number 1, June 2004 , pp. 49-55(7)
Publisher: Expert Reviews
- Expert Review of Proteomics explores technologies, methods and discoveries from the field of proteomics to advance scientific understanding of the many varied roles protein expression plays in human health and disease.
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Abstract:
Oncoproteomics is the term used to describe the application of proteomic technologies in oncology and parallels the related field of oncogenomics. It is now contributing to the development of personalized management of cancer. Proteomic technologies are used for the identification of biomarkers in cancer, which will facilitate the integration of diagnosis and therapy of cancer. Molecular diagnostics, laser capture microdissection and protein biochips are among the technologies that are having an important impact on oncoproteomics. The discovery of protein patterns developed by the US Food and Drug Administration/National Cancer Institute Clinical Proteomics Program is capable of distinguishing cancer and disease-free states with high sensitivity and specificity and will also facilitate the development of personalized therapy of cancer. Examples of application are given for breast and prostate cancer and a selection of companies and their collaborations that are developing application of proteomics to personalized treatment of cancer are discussed. Continued refinement of techniques and methods to determine the abundance and status of proteins in vivo holds great promise for the future study of normal cells and the pathology of associated neoplasms. Personalized cancer therapy is expected to be in the clinic by the end of the first decade of the 21st century.Keywords: biomarkers; cancer; laser capture microdissection; molecular diagnostics; oncogenomics; oncoproteomics; personalized medicine; protein microarrays/biochips; protein patterns; protein profiling; proteomics
Document Type: Research article
DOI: 10.1586/14789450.1.1.49
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