Dimethylbenzanthracene carcinogenesis in Gadd45a-null mice is associated with decreased DNA repair and increased mutation frequency

M. Christine Hollander, Oleg Kovalsky, Jesus M. Salvador, Kate E. Kim, Andrew D. Patterson, Diana C. Haines, Albert J. Fornace

Research output: Contribution to journalArticle

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Abstract

Mice lacking the Gadd45a gene are susceptible to ionizing radiation-induced tumors. Increased levels of Gadd45a transcript and protein are seen after treatment of cells with ionizing radiation as well as many other agents and treatments that damage DNA. Because cells deficient in Gadd45a were shown to have a partial defect in the global genomic repair component of the nucleotide excision repair pathway of UV-induced photoproducts, dimethylbenzanthracene (DMBA) carcinogenesis was investigated because this agent produces bulky adducts in DNA that are also repaired by nucleotide excision repair. Wild-type mice and mice deficient for Gadd45a were injected with a single i.p. dose of DMBA at 10-14 days of age. The latency for spontaneous deaths was slightly decreased for Gadd45a-null mice compared with wild-type mice. At 17 months, all surviving animals were killed, and similar percentages of each genotype were found to have tumors. However, nearly twice as many Gadd45a-null than wild-type mice had multiple tumors, and three times as many had multiple malignant tumors. The predominant tumor types in wild-type mice were lymphoma and tumors of the intestines and liver. In Gadd45a-null mice, there was a dramatic increase in female ovarian tumors, male hepatocellular tumors, and in vascular tumors in both sexes. In wild-type mice, this dose of DMBA induced a >5-fold increase in Gadd45a transcript in the spleen and ovary, whereas the increase in liver was >20-fold. Nucleotide excision repair, which repairs both UV- and DMBA-induced DNA lesions, was substantially reduced in Gadd45a-null lymphoblasts. Mutation frequency after DMBA treatment was threefold higher in Gadd45a-null liver compared with wild-type liver. Therefore, lack of basal and DMBA-induced Gadd45a may result in enhanced tumorigenesis because of decreased DNA repair and increased mutation frequency. Genomic instability, decreased cell cycle checkpoints, and partial loss of normal growth control in cells from Gadd45a-null mice may also contribute to this process.

Original languageEnglish (US)
Pages (from-to)2487-2491
Number of pages5
JournalCancer Research
Volume61
Issue number6
StatePublished - Mar 15 2001

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Mutation Rate
DNA Repair
Carcinogenesis
Neoplasms
Liver
Ionizing Radiation
Null Lymphocytes
DNA Adducts
Genomic Instability
Cell Cycle Checkpoints
DNA Damage
Intestines
Blood Vessels
Ovary
Lymphoma
Spleen
Genotype
DNA

All Science Journal Classification (ASJC) codes

  • Oncology
  • Cancer Research

Cite this

Hollander, M. C., Kovalsky, O., Salvador, J. M., Kim, K. E., Patterson, A. D., Haines, D. C., & Fornace, A. J. (2001). Dimethylbenzanthracene carcinogenesis in Gadd45a-null mice is associated with decreased DNA repair and increased mutation frequency. Cancer Research, 61(6), 2487-2491.
Hollander, M. Christine ; Kovalsky, Oleg ; Salvador, Jesus M. ; Kim, Kate E. ; Patterson, Andrew D. ; Haines, Diana C. ; Fornace, Albert J. / Dimethylbenzanthracene carcinogenesis in Gadd45a-null mice is associated with decreased DNA repair and increased mutation frequency. In: Cancer Research. 2001 ; Vol. 61, No. 6. pp. 2487-2491.
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Hollander, MC, Kovalsky, O, Salvador, JM, Kim, KE, Patterson, AD, Haines, DC & Fornace, AJ 2001, 'Dimethylbenzanthracene carcinogenesis in Gadd45a-null mice is associated with decreased DNA repair and increased mutation frequency', Cancer Research, vol. 61, no. 6, pp. 2487-2491.

Dimethylbenzanthracene carcinogenesis in Gadd45a-null mice is associated with decreased DNA repair and increased mutation frequency. / Hollander, M. Christine; Kovalsky, Oleg; Salvador, Jesus M.; Kim, Kate E.; Patterson, Andrew D.; Haines, Diana C.; Fornace, Albert J.

In: Cancer Research, Vol. 61, No. 6, 15.03.2001, p. 2487-2491.

Research output: Contribution to journalArticle

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T1 - Dimethylbenzanthracene carcinogenesis in Gadd45a-null mice is associated with decreased DNA repair and increased mutation frequency

AU - Hollander, M. Christine

AU - Kovalsky, Oleg

AU - Salvador, Jesus M.

AU - Kim, Kate E.

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AU - Fornace, Albert J.

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