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Home › Dataset Library › Transcription profiling by array of rat normal bronchial epithelial cells to study the impact of TNFa on NFkB translocation and gene...

Dataset: Transcription profiling by array of rat normal bronchial epithelial cells to study the impact of TNFa on NFkB translocation and gene expression pattern

High-throughput measurement technologies produce data sets that have the potential to elucidate the biological impact of disease, drug...

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High-throughput measurement technologies produce data sets that have the potential to elucidate the biological impact of disease, drug treatment, and environmental agents on humans. The scientific community faces an ongoing challenge in the analysis of these rich data sources to more accurately characterize biological processes that have been perturbed at the mechanistic level. Here, a new approach is built on previous methodologies in which high-throughput data was interpreted using prior biological knowledge of cause and effect relationships. These relationships are structured into network models that describe specific biological processes, such as inflammatory signaling or cell cycle progression. This enables quantitative assessment of network perturbation in response to a given stimulus. Four complementary methods were devised to quantify treatment-induced activity changes in processes described by network models. In addition, companion statistics were developed to qualify significance and specificity of the results. This approach is called Network Perturbation Amplitude (NPA) scoring because the amplitudes of treatment-induced perturbations are computed for biological network models. The NPA methods were tested on two transcriptomic data sets: normal human bronchial epithelial (NHBE) cells treated with the pro-inflammatory signaling mediator TNFa, and HCT116 colon cancer cells treated with the CDK cell cycle inhibitor R547. Each data set was scored against network models representing different aspects of inflammatory signaling and cell cycle progression, and these scores were compared with independent measures of pathway activity in NHBE cells to verify the approach. The NPA scoring method successfully quantified the amplitude of TNFa-induced perturbation for each network model when compared against NF-kB nuclear localization and cell number. In addition, the degree and specificity to which CDK-inhibition affected cell cycle and inflammatory signaling were meaningfully determined. The NPA scoring method leverages high-throughput measurements and a priori literature-derived knowledge in the form of network models to characterize the activity change for a broad collection of biological processes at high-resolution. Applications of this framework include comparative assessment of the biological impact caused by environmental factors, toxic substances, or drug treatments.

Species:
rat

Samples:
45

Source:
E-MTAB-1311

Updated:
Feb.09, 2015

Registered:
Jan.12, 2015


Factors: (via ArrayExpress)
Sample dose TNFAsamplingTimepoint compound
13674_RLAK_196 0.5 vehicle control (sham)
13674_RLAK_196 0.5 vehicle control (sham)
13674_RLAK_196 0.5 vehicle control (sham)
13674_RLAK_199 0.1 0.5 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_199 0.1 0.5 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_199 0.1 0.5 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_202 1 0.5 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_202 1 0.5 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_202 1 0.5 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_205 10 0.5 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_205 10 0.5 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_205 10 0.5 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_208 100 0.5 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_208 100 0.5 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_208 100 0.5 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_211 2.0 vehicle control (sham)
13674_RLAK_211 2.0 vehicle control (sham)
13674_RLAK_211 2.0 vehicle control (sham)
13674_RLAK_214 0.1 2.0 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_214 0.1 2.0 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_214 0.1 2.0 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_217 1 2.0 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_217 1 2.0 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_217 1 2.0 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_220 10 2.0 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_220 10 2.0 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_220 10 2.0 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_223 100 2.0 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_223 100 2.0 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_223 100 2.0 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_226 24.0 vehicle control (sham)
13674_RLAK_226 24.0 vehicle control (sham)
13674_RLAK_226 24.0 vehicle control (sham)
13674_RLAK_229 0.1 24.0 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_229 0.1 24.0 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_229 0.1 24.0 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_232 1 24.0 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_232 1 24.0 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_232 1 24.0 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_235 10 24.0 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_235 10 24.0 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_235 10 24.0 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_238 100 24.0 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_238 100 24.0 Recombinant Tumor Necrosis Factor-Alpha
13674_RLAK_238 100 24.0 Recombinant Tumor Necrosis Factor-Alpha

Tags

  • cancer
  • cell
  • colon
  • colon cancer
  • disease

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