Cancer development and progression
- PMID: 17265722
- DOI: 10.1007/978-0-387-39978-2_12
Cancer development and progression
Abstract
Cancer development and progression is a complex process that involves a host of functional and genetic abnormalities. Genomic perturbations and the gene expression they lead to, can now be globally identified with the use of DNA microarray. This relatively new technology has forever changed the scale of biological investigation. The enormous amount of data generated via a single chip has led to major global studies of the cellular processes underlying malignant transformation and progression. The multiplicity of platforms from different proprietors has offered investigators flexibility in their experimental design. Additionally, there are several more recent microarrays whose designs were inspired by the nucleotide-based technology. These include protein, multi-tissue, cell, and interference RNA microarrays. Combinations of microarray and other contemporary scientific methods, such as, laser capture microdissection (LCM), comparative genomic hybridization (CGH), single nucleotide polymorphism analysis (SNP) and chromatin immunoprecipitation (ChIP), have created entirely new fields of interest in the more global quest to better define the molecular basis of malignancy. In addition to basic science applications, many clinical inquiries have been performed. These queries have shown microarray to have clinical utility in cancer diagnosis, risk stratification, and patient management.
Similar articles
-
Microarray tools for deciphering complex diseases.Front Biosci. 2006 May 1;11:1414-24. doi: 10.2741/1892. Front Biosci. 2006. PMID: 16368525 Review.
-
Applications of DNA tiling arrays for whole-genome analysis.Genomics. 2005 Jan;85(1):1-15. doi: 10.1016/j.ygeno.2004.10.005. Genomics. 2005. PMID: 15607417 Review.
-
Differential gene alteration among hepatoma cell lines demonstrated by cDNA microarray-based comparative genomic hybridization.Biochem Biophys Res Commun. 2005 Apr 1;329(1):370-80. doi: 10.1016/j.bbrc.2005.01.128. Biochem Biophys Res Commun. 2005. PMID: 15721316
-
Improving reliability and performance of DNA microarrays.Expert Rev Mol Diagn. 2006 May;6(3):481-92. doi: 10.1586/14737159.6.3.481. Expert Rev Mol Diagn. 2006. PMID: 16706748 Review.
-
Microarrays--chances and challenges.Curr Opin Mol Ther. 1999 Dec;1(6):727-36. Curr Opin Mol Ther. 1999. PMID: 19629870 Review.
Cited by
-
Genome-wide profiling using single-nucleotide polymorphism arrays identifies novel chromosomal imbalances in pediatric glioblastomas.Neuro Oncol. 2010 Feb;12(2):153-63. doi: 10.1093/neuonc/nop001. Epub 2009 Oct 15. Neuro Oncol. 2010. PMID: 20150382 Free PMC article.
-
Mapping mitochondrial heteroplasmy in a Leydig tumor by laser capture micro-dissection and cycling temperature capillary electrophoresis.BMC Clin Pathol. 2017 Apr 8;17:6. doi: 10.1186/s12907-017-0042-3. eCollection 2017. BMC Clin Pathol. 2017. PMID: 28405177 Free PMC article.
-
Linear and non-linear dependencies between copy number aberrations and mRNA expression reveal distinct molecular pathways in breast cancer.BMC Bioinformatics. 2011 May 24;12:197. doi: 10.1186/1471-2105-12-197. BMC Bioinformatics. 2011. PMID: 21609452 Free PMC article.
-
Microarray analysis of cutaneous squamous cell carcinomas reveals enhanced expression of epidermal differentiation complex genes.Mol Carcinog. 2010 Jul;49(7):619-29. doi: 10.1002/mc.20636. Mol Carcinog. 2010. PMID: 20564339 Free PMC article.
-
Down-Regulation of C3aR/C5aR Inhibits Cell Proliferation and EMT in Hepatocellular Carcinoma.Technol Cancer Res Treat. 2020 Jan-Dec;19:1533033820970668. doi: 10.1177/1533033820970668. Technol Cancer Res Treat. 2020. PMID: 33176600 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources