| Literature DB >> 10851081 |
H Maacke1, K Jost, S Opitz, S Miska, Y Yuan, L Hasselbach, J Lüttges, H Kalthoff, H W Stürzbecher.
Abstract
Molecular processes that could contribute to differences in chemo- and radioresistance include variations in DNA repair mechanisms. In mammalian cells, the product of the rad51 gene mediates DNA repair via homologous recombination. We describe that in contrast to conventional monolayer cell systems Rad51 protein accumulates to high-levels in three-dimensional cell culture models as well as in orthotopic xeno-transplants of human pancreatic cancer cells. Strikingly, over-expression of wild-type Rad51 was also found in 66% of human pancreatic adenocarcinoma tissue specimens. Functional analysis revealed that Rad51 over-expression enhances survival of cells after induction of DNA double strand breaks. These data suggest that perturbations of Rad51 expression contribute to the malignant phenotype of pancreatic cancer. Oncogene (2000).Entities:
Mesh:
Substances:
Year: 2000 PMID: 10851081 DOI: 10.1038/sj.onc.1203578
Source DB: PubMed Journal: Oncogene ISSN: 0950-9232 Impact factor: 9.867