Swim Across America grants $900,000 toward first-of-its-kind gene editing innovation
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Updates every hour. Last Updated: 26-Apr-2025 21:08 ET (27-Apr-2025 01:08 GMT/UTC)
Shawn Demehri, MD, PhD, a physician-investigator in the Cutaneous Biology Research Center and Krantz Family Center for Cancer Research at Massachusetts General Hospital and an Associate Professor of Dermatology at Harvard Medical School in the senior author of a new study in Cell Reports, Epigenomic Regulation of Stemness Contributes to the Low Immunogenicity of the Most Mutated Human Cancer.
Colorectal cancer (CRC) is a globally prevalent malignancy with high morbidity and mortality rates, closely linked to aberrant epigenetic modifications. Among these, pseudouridine (Ψ), one of the most abundant RNA chemical modifications, plays a pivotal role in tumorigenesis by regulating mRNA stability, translation efficiency, and splicing processes. Recent studies have demonstrated that the small-molecule inhibitor Pyrazofurin, targeting the pseudouridine synthase DKC1, exhibits significant anti-tumor activity, suggesting Ψ modification as a promising therapeutic strategy for CRC. However, the dynamic changes and clinical implications of transcriptome-wide Ψ modifications in CRC remain poorly understood.
In an original research article published in MedComm - Oncology, an antiallergic drug fexofenadine was identified as a new Met inhibitory agent by a computational drug repurposing tool called “DRAR-CPI” via chemical-protein interactome analysis of known Met inhibitors. Fexofenadine was shown to overcome osimertinib resistance in non-small cell lung cancer by inhibiting Met in vitro and in vivo.
Among adults ages 18-49 (median age of 41 years) who were born with a hole in the upper chambers of their heart known as patent foramen ovale (PFO), strokes of unknown cause were more strongly associated with nontraditional risk factors, such as migraines, liver disease or cancer, rather than more typical factors such as high blood pressure.