| Literature DB >> 7505724 |
F Cortés1, N Panneerselvam, S Mateos, T Ortiz.
Abstract
Cultured CHO cells were treated with the radiomimetic antitumor agent bleomycin (BLM) and post-treated with the polycationic compound poly-D-lysine (PDL), recently reported by us as able to potentiate chromosome damage induced by X-rays and chemical mutagens in both plant and mammalian cells. Our results seem to indicate that PDL enhances the genotoxic action of BLM measured as induced chromosomal aberrations, colony-forming ability and DNA strand breakage. Taking into account the reported low efficiency of BLM treatment due to problems with cellular uptake, enzymatic degradation and efficient repair, the possibility of optimizing the dose-effectiveness for cancer therapy is discussed.Entities:
Mesh:
Substances:
Year: 1993 PMID: 7505724 DOI: 10.1093/carcin/14.12.2543
Source DB: PubMed Journal: Carcinogenesis ISSN: 0143-3334 Impact factor: 4.944