echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Active Ingredient News > Immunology News > PNAS: Split immunotoxins in two or hopefully kill cancer cells with precision without damaging the function of healthy cells.

    PNAS: Split immunotoxins in two or hopefully kill cancer cells with precision without damaging the function of healthy cells.

    • Last Update: 2020-09-26
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com
    14, 2020 // -- In a recent study published in the international journal PNAS, scientists from Ohio State University and other institutions found that spliting an anticancer drug in two and then giving cancer cells or effectively reducing their life-threatening side effects, while protecting healthy non-cancerous cells from being affected;
    Photo Source: CC0 Public Domain Immunotoxin combines immunological substances with toxins that absorb cancer cells, which promote toxins into cancer cells and kill them without damaging nearby healthy cells; the study was designed as a proof-of-concept study, but the researchers found that they were able to reconstruct the functional toxin in cell cultures in laboratories and cancer cells in mice.
    Scientists' research into cancer therapies has now helped develop a number of effective treatments that not only destroy cancer cells, but also healthy non-cancerous cells, and that can have life-threatening side effects; the problem, says researcher Dmitri Kudryashov, is that we don't want to kill healthy cells, and the challenge now is how to kill only cancer cells without affecting their function.
    When certain cancer therapies can successfully target cancer cells, perhaps few can accurately kill cancer cells without affecting the function of healthy cells, the key to dividing immunotoxins is that only cancer cells can accept the two parts of the division toxin, the researchers confirmed that when separated, the division toxin part does not damage healthy cells, but when it is reassembled into the original toxin, the therapy can destroy cancer. To achieve this, both parts of the immunotoxin must go into cancer cells, and so far the researchers have achieved that the toxin, which reconstructs this complete function after transporting one part of the divided immune toxin to the cells that express the other part, while the other part of the specific transport may yet be studied further, is still being studied, said
    researcher Elena Kudryashova.
    In essence, the researchers say, when toxin proteins enter the body later in life as a cancer treatment, but they do not cause damage to healthy cells, and if biochemists can find a way to transport both parts of the toxin protein to cancer cells, both parts of the toxin may be expected to destroy cancer cells.
    () Original source: Vedud Purde, Elena Kudryashova, David B. Heisler, et al. Intein-mediated cytoplasmic reconstitution of a split toxin enables selective cell ablation in mixed populations and tumors xenografts, PNAS (2020) doi:10.1073/pnas.2006603117.
    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.