Abstract
Cancer gene profiling has greatly profited from the progress in high-throughput technologies including microarray-, sequencing-, and bioinformatics-based methods. The flood of data generated during the last decade has provoked a panel of “-omics” fields that significantly changed our understanding of malignant diseases. However, while the terms “-omics” and “-ome” in principle refer to the completeness of a genetic approach, we are in fact far from a complete understanding of cancer progression. We may understand gene expression patterns better and successfully use gene signatures for outcome prediction and prognosis, but truly promising molecular targets still have to find their way into novel therapeutic concepts. In this chapter, we will show how more comprehensive strategies, integrating multiple layers of genetic information, might in the future provide a more profound functional understanding of cancer.
| Original language | English |
|---|---|
| Title of host publication | Cancer Gene Profiling |
| Subtitle of host publication | Methods and Protocols |
| Editors | Robert Grützmann, Christian Pilarsky |
| Publisher | Humana Press |
| Pages | 61-87 |
| ISBN (Electronic) | 978-1-59745-545-9 |
| ISBN (Print) | 978-1-934115-76-3, 978-1-61779-659-3 |
| DOIs | |
| Publication status | Published - 2010 |
| MoE publication type | A3 Part of a book or another research book |
Publication series
| Series | Methods in Molecular Biology |
|---|---|
| Volume | 576 |
| ISSN | 1064-3745 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
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SDG 11 Sustainable Cities and Communities
Keywords
- Microarray
- Expression
- CGH
- Comparative genomic hybridization
- Sequencing
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