Publications by authors named "A S Hundt"

Article Synopsis
  • RIPTACs (Regulated Induced Proximity Targeting Chimeras) are innovative small molecules designed to create stable complexes between a target protein found in tumor cells and a widely expressed essential protein, leading to cancer cell death.
  • This approach targets proteins that are specifically expressed in cancer cells without needing them to be the main drivers of the disease, thus offering a new strategy for cancer treatment.
  • In the study, RIPTACs were engineered with ligands linked to various effector molecules, demonstrating selective accumulation in target-expressing cells and effectively inducing an anti-proliferative effect.
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While specific cell signaling pathway inhibitors have yielded great success in oncology, directly triggering cancer cell death is one of the great drug discovery challenges facing biomedical research in the era of precision oncology. Attempts to eradicate cancer cells expressing unique target proteins, such as antibody-drug conjugates (ADCs), T-cell engaging therapies, and radiopharmaceuticals have been successful in the clinic, but they are limited by the number of targets given the inability to target intracellular proteins. More recently, heterobifunctional small molecules such as Proteolysis Targeting Chimera (PROTACs) have paved the way for protein proximity inducing therapeutic modalities.

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Background: Cardiac arrest (CA) represents the third leading cause of death worldwide. Among patients resuscitated and admitted to hospital, death and severe neurological sequelae are frequent but difficult to predict. Blood biomarkers offer clinicians the potential to improve prognostication.

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