Genetic analysis of pulmonary adenocarcinomas and precursors
Genetic analysis of pulmonary adenocarcinomas and precursors
Disciplines
Medical-Theoretical Sciences, Pharmacy (100%)
Keywords
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MICROARRAY MOLECULAR-CYTOGENETIC,
ADENOCARCINOMA,
AAH DYSPLASIA,
GENE EXPRESSION STUDY
Molecular-cytogenetic and gene expression study of adenocarcinomas and its possible precursor lesions Adenocarcinomas (AC) have become the major group of lung carcinomas in Austria as well as world-wide. In the last decade precursor lesions of AC especially atypical adenomatous hyperplasia have gained particular interest. One intention of the submitted project is the identification of oncogenes and tumorsuppressor genes responsible for progression and differentiation of ACs. The expression of these genes will also be checked at the protein level. As a result of this study we hope to find several biomarkers easily detectable by usual immunhistochemistry and therefore feasible for clinical routine. However, we additionally want to enlight another aspect. Tumor cells are following the evolutionary priniciple, making the most fittest clone the pivotal one. Under this view we will investigate, how tumor cells react to gross chromosomal aberrations. In our opinion, first the cells have to reestablish a kind of balance in order to stay alive, and second, they have to adapt their biochemical pathways in order to fully exploit the growth advantage provided by the genetic alteration. For example, there would be no use of a high copy amplified oncogene, if it has to form a heterodimer with an other not overrepresented protein in order to exert its influence. By this analysis we hope to get further insights into transcriptional control and to elucidate interconnected genes and redundant pathways. Taking advantage of the tremendous progress of the Human Genome Project we also want to reveal sequence dependency of selected chromosomal breakpoints. Integration of sequence data and gene expression data for genes in the vicinity of the breakpoints should clarify the question why some chromosomal sites are more vulnerable than others and why this preference is tissue and tumor specific in many cases. This study will utilize Comparative Genomic Hybridization (CGH), microarray CGH and gene expression studies as well as immunhistochemistry and FISH on tissuearrays.
Research Output
- 225 Citations
- 5 Publications
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2004
Title Protein expression profiles in adenocarcinomas and squamous cell carcinomas of the lung generated using tissue microarrays DOI 10.1002/path.1584 Type Journal Article Author Ullmann R Journal The Journal of Pathology Pages 798-807 -
2004
Title Analysis of chromosome-11 aberrations in pulmonary and gastrointestinal carcinoids: an array comparative genomic hybridization-based study DOI 10.1007/s00428-004-1052-y Type Journal Article Author Petzmann S Journal Virchows Archiv Pages 151-159 -
2004
Title Atypical goblet cell hyperplasia in congenital cystic adenomatoid malformation as a possible preneoplasia for pulmonary adenocarcinoma in childhood: a genetic analysis DOI 10.1016/j.humpath.2004.01.008 Type Journal Article Author Stacher E Journal Human Pathology Pages 565-570 Link Publication -
2004
Title Distinct sequences on 11q13.5 and 11q23–24 are frequently coamplified with MLL in complexly organized 11q amplicons in AML/MDS patients DOI 10.1002/gcc.20002 Type Journal Article Author Zatkova A Journal Genes, Chromosomes and Cancer Pages 263-276 -
2003
Title Bronchiolar columnar cell dysplasia—genetic analysis of a novel preneoplastic lesion of peripheral lung DOI 10.1007/s00428-003-0797-z Type Journal Article Author Ullmann R Journal Virchows Archiv Pages 429-436