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Updated: May 12, 2026

Radiolabeling and Quantification of Cellular Levels of Phosphoinositides by High Performance Liquid Chromatography-coupled Flow Scintillation
Published on: January 6, 2016
Nuclear phosphoinositide signaling in cell biology and disease
Yanan Sun1, Fengting Liu1, Chunbo Chen2
1Department of Critical Care Medicine, Shenzhen People's Hospital, The Second Clinical Medical College, Jinan University, The First Affiliated Hospital, Southern University of Science and Technology, Shenzhen 518020, China; Department of Geriatrics, Guangdong Provincial Clinical Research Center for Geriatrics, Shenzhen Clinical Research Center for Geriatrics, Shenzhen People's Hospital, Shenzhen 518020, China; Laboratory of Oral Homeostatic Medicine, School of Medicine and SUSTech Homeostatic Medicine Institute (SHMI), Southern University of Science and Technology, Shenzhen 518055, China; Department of Pharmacology, Joint Laboratory of Guangdong-Hong Kong Universities for Vascular Homeostasis and Diseases, School of Medicine and SUSTech Homeostatic Medicine Institute (SHMI), Southern University of Science and Technology, Shenzhen 518055, China.
Abstract:
Phosphatidylinositol phosphates (PIPs), or phosphoinositides, are minor yet essential phospholipids that govern diverse cellular processes, from membrane trafficking to signal transduction. While traditionally studied within the cell membranes, emerging evidence reveals their dynamic metabolism and critical functions in the nucleus, particularly within the non-membrane nucleoplasm, continually reshaping our understanding of the nuclear PIP-lipidome and its therapeutic potential. However, an updated overview of the nuclear PIP landscape and its selective modulators remains lacking. This review addresses this gap by providing an integrated summary of nuclear PIP signaling components, encompassing their structures, species, distribution, transport, and metabolic regulation. A focus is placed on pharmacological modulation, including inhibitors and activators targeting nuclear phosphatidylinositol (PI/PtdIns) transfer proteins and PIP-metabolizing enzymes, with attention to structure-based inhibitor classes and representative clinical-stage compounds. We conclude by outlining therapeutic opportunities that arise from targeting the nuclear PIP pathway, particularly in the context of cancer, cardiovascular disease, and neurodegeneration.
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