This review focuses on the critical role of amino acid metabolism in breast cancer development and progression. It explains how cancer cells reprogram amino acid usage—especially glutamine, serine, glycine, aspartate, arginine, and tryptophan—to support proliferation, survival, immune evasion, and metastasis. The review emphasizes metabolic heterogeneity among different breast cancer subtypes and explores therapeutic strategies targeting these pathways.

This review article provides a comprehensive overview of stress granules (SGs) —membraneless organelles formed in response to cellular stress—and their interactions with other organelles. It explores their structure, function, roles in health and disease, especially neurodegeneration, and discusses methodologies used to study these interactions. SGs influence critical cellular pathways, and understanding their interplay with both membrane-bound and membraneless organelles can reveal potential therapeutic targets for diseases like ALS and FTD.

Researchers from the National University of Singapore (NUS) have solved a 60-year-old mystery in bacterial cell envelope biology, defining the primary function of an important protein complex responsible for maintaining the stability of the outer membrane (OM).

Chrysanthemums—prized for their beauty and medicinal value—have long lacked a centralized, data-rich research platform. That's about to change. 

It’s a debilitating disease that affects more than 500,000 Australians, but new research from the University of South Australia is offering fresh hope to people living with rheumatoid arthritis (RA).

The review highlights how disrupting the cell cycle, a process often hijacked by cancer cells for unchecked growth offers a promising strategy for cancer therapy. It focuses on drugs that precisely target key cell cycle regulators, several of which are already in clinical use. By showcasing the latest breakthroughs and outlining future research directions, the article provides a comprehensive look at how targeting cell cycle dysregulation is shaping the future of cancer care.

Researchers have unveiled the transformative potential of micropattern arrays—engineered microstructures—to probe and guide cellular biomechanics. These arrays not only help decipher how cells sense physical cues but also steer tissue regeneration and stem cell fate, paving the way for breakthroughs in tissue regeneration, organ-on-a-chip systems, and disease modeling.