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Apr 2, 2007

Upstream Taps NimbleGen for Cancer Biomarker Validation Studies

  • Upstream Biosciences appointed NimbleGen Systems to provide laboratory services. NimbleGen will use its whole genome chromatin immunoprecipitation (ChIP)-chip arrays and laboratory services to validate Upstream's in silico binding site predictions.

    Upstream utilizes data mining techniques to identify regulatory regions of the genome upstream of genes that have been clinically identified as being involved in various disease and drug response processes. It currently has five provisional patent filings covering the use of certain genetic variations in these regulatory regions as diagnostic markers for various forms of cancer.

    "These studies will use clinical samples of prostate and liver cancer and normal samples to help validate the effectiveness of our proprietary biomarker candidates," says CEO Joel Bellenson. "NimbleGen's arrays cover the gene promoter sequences of the entire human genome and may allow us to probe for DNA-binding sites that match the DNA-binding proteins present in diseased and normal tissue."

     



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Scientifically Studying Ecstasy

MDMA (commonly known as the empathogen “ecstasy”) is classified as a Schedule 1 drug, which is reserved for compounds with no accepted medical use and a high abuse potential. Two researchers from Stanford, however, call for a rigorous scientific exploration of MDMA's effects to identify precisely how the drug works, the data from which could be used to develop therapeutic compounds.

Do you agree that ecstasy should be studied for its potential therapeutic benefits?

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