Format

Send to

Choose Destination
Cell Cycle. 2015;14(2):206-18. doi: 10.4161/15384101.2014.974425.

Chromosome segregation and organization are targets of 5'-Fluorouracil in eukaryotic cells.

Author information

1
a Instituto de Biología Molecular "Eladio Viñuela" (CSIC), Centro de Biología Molecular "Severo Ochoa" (CSIC-Universidad Autónoma) ; Cantoblanco , Madrid , Spain.

Abstract

The antimetabolite 5'-Fluorouracil (5FU) is an analog of uracil commonly employed as a chemotherapeutic agent in the treatment of a range of cancers including colorectal tumors. To assess the cellular effects of 5FU, we performed a genome-wide screening of the haploid deletion library of the eukaryotic model Schizosaccharomyces pombe. Our analysis validated previously characterized drug targets including RNA metabolism, but it also revealed unexpected mechanisms of action associated with chromosome segregation and organization (post-translational histone modification, histone exchange, heterochromatin). Further analysis showed that 5FU affects the heterochromatin structure (decreased levels of histone H3 lysine 9 methylation) and silencing (down-regulation of heterochromatic dg/dh transcripts). To our knowledge, this is the first time that defects in heterochromatin have been correlated with increased cytotoxicity to an anticancer drug. Moreover, the segregation of chromosomes, a process that requires an intact heterochromatin at centromeres, was impaired after drug exposure. These defects could be related to the induction of genes involved in chromatid cohesion and kinetochore assembly. Interestingly, we also observed that thiabendazole, a microtubule-destabilizing agent, synergistically enhanced the cytotoxic effects of 5FU. These findings point to new targets and drug combinations that could potentiate the effectiveness of 5FU-based treatments.

KEYWORDS:

5FU, 5′-Fluorouracil, 5FU; 5′-Fluorouracil; Anticancer drug; CENP-A, centromere-associated protein A; CLRC, Clr4 methyltransferase complex; ChIP, chromatin immunoprecipitation; FUTP, fluorouridine triphosphate; FdUMP, fluorodeoxyuridine monophosphate; FdUTP, fluorodeoxyuridine triphosphate; G1 phase, gap 1 phase of cell cycle; GO, Gene Ontology; H3K9me, H3 lysine 9 methylation; HAT, histone acetyltransferase; HDAC, histone deacetylase; HMT, histone methyltransferase; HP1, heterochromatin protein 1; HULC, histone H2B ubiquitin ligase complex; MNAse, micrococcal nuclease; RDRC, RNA-directed RNA polymerase complex; RITS, RNA-induced transcriptional silencing; RNAi, interference RNA; S phase, synthesis phase of cell cycle; Schizosaccharomyces pombe; TBZ, thiabendazole; centromere; chromosome organization; chromosome segregation; cnt, central core; dsRNA, double-stranded RNA; heterochromatin; histone modification; imr, innermost repeats; siRNA, small interfering RNA

PMID:
25483073
PMCID:
PMC4352961
DOI:
10.4161/15384101.2014.974425
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for Taylor & Francis Icon for PubMed Central
Loading ...
Support Center