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BioWorld - Tuesday, May 12, 2026

Cancer

Home » Topics » Disease categories and therapies » Cancer
  • T cell gray and red
    May 11, 2026
    By Mar de Miguel

    In vivo mRNA gene therapy platform reprograms cytotoxic T cells

    A new mRNA and lipid nanoparticle (mRNA-LNP) platform could selectively reprogram in vivo cytotoxic effector T cells (Teff), the cells responsible for eliminating infected or tumor cells. To achieve this, scientists at the University of Pennsylvania conjugated LNPs with fractalkine, a molecule that binds to the CX3CR1 receptor, which is a marker of Teff cells. Using this strategy, the researchers delivered an mRNA encoding new proteins such as IL‑2 or human CD62 L‑selectin, opening the door to temporarily reprogramming these cells within the body, both in the blood and in lymphoid tissue, where they reside and become activated.
  • May 11, 2026

    Yantai Rongchang Pharmaceutical reports new KRAS mutant inhibitors

    Yantai Rongchang Pharmaceutical Co. Ltd. has synthesized new GTPase KRAS mutant inhibitors potentially useful for the treatment of pancreatic cancer.
  • May 11, 2026

    Hefei Shengpu Pharmaceutical synthesizes new GTPase KRAS mutant inhibitors

    Hefei Shengpu Pharmaceutical Technology Co. Ltd. has divulged new GTPase KRAS mutant inhibitors potentially useful for the treatment of cancer.
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