echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Biochemistry News > Biotechnology News > Science Sub-Journal: A new method to eradicate breast cancer

    Science Sub-Journal: A new method to eradicate breast cancer

    • Last Update: 2021-07-27
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com

    A new treatment for breast cancer killed 95-100% of cancer cells in mouse models of human estrogen receptor-positive breast cancer and their metastases in bone, brain, liver, and lungs


    A research team led by scientists at the University of Illinois at Urbana-Champaign reported the discovery in the journal Science Translational Medicine


    "Even if a small number of breast cancer cells survive, allowing the tumor to regenerate within a few months, the regenerated tumor is still fully susceptible to ErSO retreatment," said David Shapiro, a professor of biochemistry at the University of Michigan, who and Illinois State chemistry professor Paul Hegenrosser led the research together


    The activity of ErSO depends on a protein called the estrogen receptor, which is present in a high percentage of breast tumors


    Shapiro said: "a-upr has been activated, but it is at a low level in many breast cancer cells


    Shapiro and former University of Michigan medical scholar Neal Andruska first discovered the a-upr pathway in 2014 and reported the development of a compound that promotes the acceleration and selectivity of the a-upr pathway To kill breast cancer cells that contain estrogen receptors


    Graduate student Darjan Duraki said: "Because this pathway has been turned on in cancer cells, we can easily overactivate it, thereby turning breast cancer cells into lethal mode


    Although the original compound prevented the growth of breast cancer cells, it did not kill them quickly, and it also produced unpleasant side effects


    "This expected UPR depends on the estrogen receptor," Hergenrother said


    Shapiro said that ErSO is different from drugs commonly used to treat estrogen receptor-positive cancers


    He said: "This is not another version of tamoxifen or haloperidol.


    Boudreau said: "Since about 75% of breast cancers are positive for estrogen receptors, ErSO has the potential to fight the most common breast cancer


    Further research has shown that exposure to drugs has no effect on their reproductive development


    Researchers report that ErSO can also act quickly, even on advanced human breast cancer tumors in mice


    Shapiro said: "Many breast cancer patients have reduced by more than 99% in just three days


    The researchers said that Bayer Pharmaceuticals has approved the new drug and will explore its potential for further research in human clinical trials for estrogen receptor-positive breast cancer


    ###

    The paper "A small-molecule activator of the unfolded protein response eradicates human breast tumors in mice" is available online and from the U.
    of I.
    News Bureau.
    DOI: 10.
    1126/scitranslmed.
    abf1383

    This article is an English version of an article which is originally in the Chinese language on echemi.com and is provided for information purposes only. This website makes no representation or warranty of any kind, either expressed or implied, as to the accuracy, completeness ownership or reliability of the article or any translations thereof. If you have any concerns or complaints relating to the article, please send an email, providing a detailed description of the concern or complaint, to service@echemi.com. A staff member will contact you within 5 working days. Once verified, infringing content will be removed immediately.

    Contact Us

    The source of this page with content of products and services is from Internet, which doesn't represent ECHEMI's opinion. If you have any queries, please write to service@echemi.com. It will be replied within 5 days.

    Moreover, if you find any instances of plagiarism from the page, please send email to service@echemi.com with relevant evidence.