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Home › Dataset Library › Transcription profiling of mouse liver treated with carcinogens and controls to identify biomarkers

Dataset: Transcription profiling of mouse liver treated with carcinogens and controls to identify biomarkers

Two-year rodent bioassays play a central role in evaluating both the carcinogenic potential of a chemical and generating quantitative...

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Two-year rodent bioassays play a central role in evaluating both the carcinogenic potential of a chemical and generating quantitative information on the dose-response behavior for chemical risk assessments. The bioassays involved are expensive and time-consuming, requiring nearly lifetime exposures (two years) in mice and rats and costing $2 to $4 million per chemical. Since there are approximately 80,000 chemicals registered for commercial use in the United States and 2,000 more are added each year, applying animal bioassays to all chemicals of concern is clearly impossible. To efficiently and economically identify carcinogens prior to widespread use and human exposure, alternatives to the two-year rodent bioassay must be developed. In this study, animals were exposed for 13 weeks to two chemicals that were positive for liver tumors in the two-year rodent bioassay, two chemicals that were negative for liver tumors, and two vehicle controls. Gene expression analysis was performed on the livers of the animals to assess the potential for identifying gene expression biomarkers that can predict tumor formation in a two-year bioassay following a 13 week exposure. Experiment Overall Design: Five week old female B6C3F1 mice were exposed for 13 weeks to the following treatments: 1) 1,5-Naphthalenediamine, CAS No. 2243-62-1, feed, 2000 ppm, positive liver carcinogen; 2) 2,3-Benzofuran, CAS No. 271-89-6, gavage, 240 mg/kg, positive liver carcinogen; 3) N-(1-naphthyl)ethylenediamine dihydrochloride, CAS No. 1465-25-4, feed, 2000 ppm, negative liver carcinogen; 4) Pentachloronitrobenzene, CAS No. 82-68-8, feed, 8187 ppm, negative liver carcinogen; 5) Feed control; 6) Corn oil gavage control. Feed animals were exposed 7 days/week and gavage animals were exposed 5 days/week (5 ml/kg). Microarray analysis was performed on the livers of three mice per treatment group.

Species:
mouse

Samples:
18

Source:
E-GEOD-5128

PubMed:
17114358

Updated:
Dec.12, 2014

Registered:
Nov.12, 2014


Factors: (via ArrayExpress)
Sample dose compound
GSE5128GSM115680 240 2,3-Benzofuran
GSE5128GSM115681 2000 N-(1-naphthyl)ethylenediamine dihydrochloride
GSE5128GSM115681 2000 N-(1-naphthyl)ethylenediamine dihydrochloride
GSE5128GSM115681 2000 N-(1-naphthyl)ethylenediamine dihydrochloride
GSE5128GSM115684 8187 Pentachloronitrobenzene
GSE5128GSM115684 8187 Pentachloronitrobenzene
GSE5128GSM115684 8187 Pentachloronitrobenzene
GSE5128GSM115687 Corn oil vehicle control
GSE5128GSM115687 Corn oil vehicle control
GSE5128GSM115687 Corn oil vehicle control
GSE5128GSM115690 Feed control
GSE5128GSM115690 Feed control
GSE5128GSM115690 Feed control
GSE5128GSM115693 2000 1,5-Naphthalenediamine
GSE5128GSM115693 2000 1,5-Naphthalenediamine
GSE5128GSM115693 2000 1,5-Naphthalenediamine
GSE5128GSM115680 240 2,3-Benzofuran
GSE5128GSM115680 240 2,3-Benzofuran

Tags

  • central
  • liver

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