UMGCCC researchers share new findings on link between lifetime alcohol use and colorectal cancer and more at AACR 2025
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Updates every hour. Last Updated: 9-Jun-2025 03:09 ET (9-Jun-2025 07:09 GMT/UTC)
Lowering the legal tackle height in women’s rugby is proving effective in reducing head contacts between players, a world-first study suggests.
Changes to the tackle height law in women’s community rugby in Scotland is linked to reductions in head-to-head and head-to shoulder contacts, the study found.
In collaboration with Scottish Rugby and World Rugby, researchers at the University of Edinburgh used video analysis to study the impact of the lowered tackle height law which World Rugby, the sport’s governing body introduced for community rugby in an attempt to improve safety for players.
A new review in Genes and Diseases explores the central role of MYC, a master regulatory protein, in the development and progression of cancer, spotlighting its potential as a multidimensional therapeutic target. MYC is dysregulated in nearly 70% of human cancers, where it influences a vast network of biological processes including cell cycle control, metabolism, apoptosis, angiogenesis, and immune evasion. The article underscores how MYC not only drives aggressive tumor behavior but also contributes significantly to drug resistance, making it one of the most compelling yet complex targets in oncology.
The nuclear pore complex protein RANBP2 has emerged as a critical factor in the development and progression of various solid malignancies. As a SUMO E3 ligase, RANBP2 plays a pivotal role in post-translational modification, specifically SUMOylation, which is essential for regulating the cell cycle. Recent insights have highlighted the multifaceted involvement of RANBP2 in tumorigenesis, suggesting its potential as a therapeutic target for cancer treatment.
Mitochondrial DNA (mtDNA) editing has emerged as a revolutionary approach in the fight against neurodegenerative diseases (NDDs). As these diseases continue to impose a significant global health burden, the innovative use of mitochondrial gene editing offers a promising avenue to address their underlying causes. The dysfunction of mitochondria, triggered by mutations in mtDNA, is now recognized as a pivotal factor contributing to the development of several debilitating conditions, including Parkinson’s disease (PD), Alzheimer’s disease (AD), Huntington’s disease (HD), and Amyotrophic Lateral Sclerosis (ALS).