New Insights on the Addictions of Tumors

New Insights on the Addictions of Tumors
  1. New Insights on the Addictions of Tumors
    Stromal tissue may provide novel targets to disrupt tumor supply…
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New Insights on the Addictions of Tumors

Stromal tissue may provide novel targets to disrupt tumor supply lines

Article ID: 682416

Released: 5-Oct-2017 5:05 PM EDT

Source Newsroom: Sanford Burnham Prebys Medical Discovery Institute

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  • Credit: James Short

    Maria Diaz-Meco, Ph.D., is a professor in SBP's NCI-designated Cancer Institute


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Cell Metabolism, Oct 2017

All Journal News, Cancer, Cell Biology
  • SBP Medical Discovery Institute, Cancer, p62 protein, ATF4
  • Newswise — La Jolla, Calif., October 5, 2017 – Researchers at Sanford Burnham Prebys Medical Discovery Institute (SBP) and UC San Diego have shown that tumors can ensure a more reliable nutrient supply by eliminating the p62 protein in surrounding stromal tissue. Specifically, p62 deficiency helps tumors and stroma (supportive tissue outside the tumor) survive and grow, despite being deprived of glutamine, an essential amino acid.

    The study, published October 5 in Cell Metabolism, suggests that the p62 pathway in tumor stroma could be a potential anti-cancer target.

    “Cancer has traditionally been treated with chemotherapies that target oncogene addictions—the oncogenic signals that tumors use to survive,” says Maria Diaz-Meco, Ph.D., professor at SBP’s NCI-designated Cancer Center and senior author of the paper. “We are looking at the non-oncogenic addictions, which are the function of non-mutated genes that also contribute to the survival of many cancers.”

    “For example, the stroma is not the cancer, but it’s a major component that supports the tumor,” explains Diaz-Meco. “We believe that targeting metabolism, not only in mutated tumor cells but also in the stroma, will be a way to find new therapies, regardless of the cancer’s mutations.”

    Tumors must develop unique mechanisms to ensure adequate nutrient supplies. To do this, they rewire surrounding tissue, particularly cancer-associated fibroblasts in the stroma, which are hijacked to do the tumor’s bidding. Essentially, the cancer remodels its nest.

    “What happens when there’s nutrient stress?” asks Diaz-Meco. “The cancer doesn’t have supplies. In its more aggressive forms, nutrient accessibility inside the tumor becomes limited. The tumor eliminates p62 from the stroma to make the stroma more aggressive, more inflammatory and to be able to support the disease.”

    This is a common strategy in cancer, as p62 is often missing from stroma in breast, prostate, liver and other tumors.

    Diaz-Meco, along with fellow authors Jorge Moscat, Ph.D., professor and deputy director of SBP’s NCI-designation Cancer Center, and Christian Metallo, Ph.D., associate professor of bioengineering at UC San Diego, believe this stromal support could offer compelling ways to interfere with tumor supply lines. Because tumors are addicted to these mechanisms, it may be possible to target them without encountering significant resistance.

    “This offers new strategies to take advantage of the tumor’s vulnerabilities,” says Diaz-Meco. “We hope that targeting non-oncogenic addictions will generate less resistance, because the stroma is more genetically stable and does not mutate as tumor cells do during aggressive therapies.”

    In the study, the team found that reducing p62 increased ATF4, an essential transcription factor protein that instructs cells to adapt to situations in which nutrients are at a premium in the tumor microenvironment. ATF4 levels only changed in stroma, remaining constant in epithelial cells, regardless of p62 levels.

    Without ATF4, stromal cells in glutamine-free media stopped growing. Further exploration showed that p62 played a…

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