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Oct 11, 2007

Molecule that Restores Normal Gene Function in Prostate Cancer Cells Discovered

  • Researchers at Johns Hopkins Kimmel Cancer Center discovered a small molecule that may prevent prostate cancer cells from using methylation to turn off normal genes.

    “One of the proteins in the cell involved in this process is called methyl-CpG binding protein, or MBD,” says lead researcher William Nelson, M.D., Ph.D., professor of oncology and urology.

    Previous research in mice missing the MBD2 gene showed that they didn't develop intestinal polyps. Other studies found that when the gene is removed from cancer cells, suppressed genes are appropriately turned on again.

    The John Hopkins team used a two-stage, cell-based, high-throughput screen to find an antagonist for the MBD2 gene,  which prevents the protein from binding to methylated genes, and then tested these molecules in cell cultures.

    “If the protein can’t bind to the gene, then it can’t keep the gene turned off and the gene is turned back on,” adds Dr. Nelson, “so they may be very exciting lead candidates for the next generation of drugs that may help restore gene function in prostate cancer.”

    The findings were presented on October 11 at the Prostate Cancer Foundation’s annual Scientific Retreat.

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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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