Differential expression of TP53 associated genes in Fanconi anemia cells after mitomycin C and hydroxyurea treatment

Angélica Martinez, John M. Hinz, Laura Gómez, Bertha Molina, Hilda Acuña, Irene M. Jones, Sara Frias, Matthew A Coleman

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

Fanconi anemia (FA) is a rare, heritable chromosomal instability disease characterized by several congenital defects and cancer predisposition. Functional interactions between specific FA proteins and DNA damage response and repair activities have been reported, but the interplay between these mechanisms for maintaining genomic stability are not well understood. Many DNA damage response proteins are transcriptionally regulated by the tumor suppressor protein p53 (TP53), suggesting an important regulatory role for the DNA damage and stress response pathway. To better understand the association between FA and the DNA damage stress response we analyzed the levels of chromosomal damage and damage mediated gene transcription responses in lymphoblastoid cells derived from normal individuals and patients carrying the most common FA complementation group (FA-A). Chromosomal aberrations were first measured after exposure to mitomicyn C (MMC) or hydroxyurea (HU). Aliquots of the same cell were than assayed for the transcriptional response of 21 DNA damage and stress response genes using quantitative real-time PCR. The FA-A lymphoblastoid cells showed significant increases in the frequency of chromosome aberrations relative to non-FA-A lymphoblastoid lines after MMC treatment. The MMC induced damage was correlated with a general increase in expression of TP53-modulated DNA damage stress response genes involved in processes such as DNA repair, cell cycle progression, and apoptosis. Following HU treatment FA cells showed a decreased induction of CAs with much less transcriptional differences between targeted genes. Overall, the differences between the normal and FA-A cells after genotoxic treatments imply an increased activation and reliance of FA cells on the down-stream activities of TP53 for prevention of cell killing and chromosome damage from interstrand crosslinks but not for general replication arrest and double strand breaks. Furthermore, these results imply a regulatory connection between the FA pathway and activation of TP53 for responding to DNA damage. Alterations in the regulation of the DNA damage response may be related to the complex phenotypes seen in FA patients.

Original languageEnglish (US)
Pages (from-to)1-7
Number of pages7
JournalMutation Research - Genetic Toxicology and Environmental Mutagenesis
Volume656
Issue number1-2
DOIs
StatePublished - Oct 30 2008
Externally publishedYes

Fingerprint

Fanconi Anemia
Hydroxyurea
p53 Genes
Mitomycin
DNA Damage
Therapeutics
Chromosome Aberrations
DNA Repair
Genes
Fanconi Anemia Complementation Group Proteins
Tumor Suppressor Protein p53
Chromosomal Instability
Genomic Instability
Anemia
Real-Time Polymerase Chain Reaction
Cell Cycle
Chromosomes
Apoptosis
Phenotype

Keywords

  • Apoptosis
  • Cell cycle arrest
  • Fanconi anemia
  • Gene expression
  • Hydroxyurea
  • Mitomycin C
  • TP53

ASJC Scopus subject areas

  • Health, Toxicology and Mutagenesis
  • Genetics

Cite this

Differential expression of TP53 associated genes in Fanconi anemia cells after mitomycin C and hydroxyurea treatment. / Martinez, Angélica; Hinz, John M.; Gómez, Laura; Molina, Bertha; Acuña, Hilda; Jones, Irene M.; Frias, Sara; Coleman, Matthew A.

In: Mutation Research - Genetic Toxicology and Environmental Mutagenesis, Vol. 656, No. 1-2, 30.10.2008, p. 1-7.

Research output: Contribution to journalArticle

Martinez, Angélica ; Hinz, John M. ; Gómez, Laura ; Molina, Bertha ; Acuña, Hilda ; Jones, Irene M. ; Frias, Sara ; Coleman, Matthew A. / Differential expression of TP53 associated genes in Fanconi anemia cells after mitomycin C and hydroxyurea treatment. In: Mutation Research - Genetic Toxicology and Environmental Mutagenesis. 2008 ; Vol. 656, No. 1-2. pp. 1-7.
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abstract = "Fanconi anemia (FA) is a rare, heritable chromosomal instability disease characterized by several congenital defects and cancer predisposition. Functional interactions between specific FA proteins and DNA damage response and repair activities have been reported, but the interplay between these mechanisms for maintaining genomic stability are not well understood. Many DNA damage response proteins are transcriptionally regulated by the tumor suppressor protein p53 (TP53), suggesting an important regulatory role for the DNA damage and stress response pathway. To better understand the association between FA and the DNA damage stress response we analyzed the levels of chromosomal damage and damage mediated gene transcription responses in lymphoblastoid cells derived from normal individuals and patients carrying the most common FA complementation group (FA-A). Chromosomal aberrations were first measured after exposure to mitomicyn C (MMC) or hydroxyurea (HU). Aliquots of the same cell were than assayed for the transcriptional response of 21 DNA damage and stress response genes using quantitative real-time PCR. The FA-A lymphoblastoid cells showed significant increases in the frequency of chromosome aberrations relative to non-FA-A lymphoblastoid lines after MMC treatment. The MMC induced damage was correlated with a general increase in expression of TP53-modulated DNA damage stress response genes involved in processes such as DNA repair, cell cycle progression, and apoptosis. Following HU treatment FA cells showed a decreased induction of CAs with much less transcriptional differences between targeted genes. Overall, the differences between the normal and FA-A cells after genotoxic treatments imply an increased activation and reliance of FA cells on the down-stream activities of TP53 for prevention of cell killing and chromosome damage from interstrand crosslinks but not for general replication arrest and double strand breaks. Furthermore, these results imply a regulatory connection between the FA pathway and activation of TP53 for responding to DNA damage. Alterations in the regulation of the DNA damage response may be related to the complex phenotypes seen in FA patients.",
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AU - Jones, Irene M.

AU - Frias, Sara

AU - Coleman, Matthew A

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