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.