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    Home > Biochemistry News > Biotechnology News > A synthetic molecule can improve the response of some cancer patients to immunotherapy

    A synthetic molecule can improve the response of some cancer patients to immunotherapy

    • Last Update: 2021-09-19
    • Source: Internet
    • Author: User
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    Picture: The new compound EnPGC-1, which activates the mitochondria of mouse T cells, can make cancer immunotherapy more effective


    Image credit: Mindy Takamiya/Kyoto University iCeMS

    A synthetic molecule is expected to improve the response of some cancer patients to immunotherapy


    Molecules expressed by cancer cells can target receptors and inactivate anti-cancer T cells


    Ganesh Namasivayam Pandian of the Institute of Integrated Cell Material Science (iCeMS) at Kyoto University added: “One of the main reasons for this non-response is that these patients have insufficient T cells, and these T cells will also be depleted because they do not have enough.


    The team hopes to find a way to increase mitochondria in T cells to improve the response of cancer patients to PD-1 blockade monotherapy


    To do this, Sugiyama and his colleagues used a compound called pyridine-imidazole polyamide (PIP), which can be programmed to specific DNA sequences


    The research team found that EnPGC-1 activated the mitochondria of mouse T cells in the laboratory, which led to an increase in the number of T cells and their longevity


    Then, they combined EnPGC-1 with PD-1 blocking immunotherapy to treat tumor-bearing mice, and found that this strategy enhanced the mice's anti-tumor immunity and improved their survival rate


    Madhu said: "Because it is well known that PGC-1 signaling is essential for energy metabolism, EnPGC-1 also has the potential to be developed as a drug for the treatment of other diseases, such as type 2 diabetes and hyperlipidemia


    Ganesh added: "Before clinical trials of this method, further improvements are needed


    DOI:


    Article title

    Targeted Epigenetic Induction of Mitochondrial Biogenesis Enhances Antitumor Immunity in Mouse Model


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