| Literature DB >> 24996439 |
Chenjiao Yao1, Wei Du, Haibing Chen, Sheng Xiao, Lihua Huang, Fangping Chen.
Abstract
The Fanconi anemia/BRCA (FA/BRCA) pathway plays a vital role in DNA damage repair induced by DNA cross-linking agents and is closely related to drug response in cancer treatment. Here we demonstrate that the FA/BRCA pathway contributes to acquired drug resistance in adriamycin (ADR)-resistant leukemia cell lines, and disruption of this pathway partially reverses the drug resistance. We observed that ADR-resistant cells have reduced DNA interstrand cross-links (ICL) compared with ADR-sensitive cells. Western blot studies demonstrated enhanced FA protein expression in ADR-resistant cells. Using siRNA to knock down FANCF in K562/R drug-resistant cells showed increases in sensitivity to ADR and ADR-induced DNA damage, and demonstrated a direct relationship between the FA/BRCA pathway and drug sensitivity. Overexpression of FANCF in K562 drug-sensitive cells partially reproduced the drug-resistant phenotype. These results show that the FA/BRCA pathway is involved in acquired ADR resistance of leukemia cells. The FA/BRCA pathway may be a new target to reverse ADR resistance in leukemia treatment.Entities:
Keywords: DNA interstrand cross-link repair; FA/BRCA pathway; drug resistance; leukemia
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Year: 2014 PMID: 24996439 DOI: 10.3109/10428194.2014.935363
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022