Plasma membrane and nuclear phosphatidylinositol 4,5-bisphosphate signalling in cancer
Jazyk angličtina Země Velká Británie, Anglie Médium electronic
Typ dokumentu časopisecké články, přehledy
Grantová podpora
Fond F Program
Charles University
Cooperatio Program: research area "Oncology and Haematology"
Charles University
AK 42/10-1
German Research Foundation
NPO EXCELES, ID Project No. LX22NPO5102
National Institute for Cancer Research
PubMed
39915829
PubMed Central
PMC11800418
DOI
10.1186/s12944-025-02452-6
PII: 10.1186/s12944-025-02452-6
Knihovny.cz E-zdroje
- Klíčová slova
- Biocondensates, Cancer, HPV, Metastasis, Nucleus, Phosphatidylinositol 4,5-bisphosphate,
- MeSH
- buněčná membrána * metabolismus MeSH
- buněčné jádro * metabolismus MeSH
- fosfatidylinositol-4,5-difosfát * metabolismus MeSH
- lidé MeSH
- membránové mikrodomény metabolismus MeSH
- metastázy nádorů MeSH
- nádory * metabolismus patologie genetika MeSH
- signální transdukce * MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
- Názvy látek
- fosfatidylinositol-4,5-difosfát * MeSH
The development of metastasis is a leading cause of cancer-related death that involves specific changes in the plasma membrane (PM) and nucleus of cancer cells. Elevated levels of membrane lipids, including sphingomyelin, cholesterol, and phosphatidylinositol 4,5-bisphosphate (PI(4,5)P2), in the PM, contribute to changes in membrane rigidity, lipid raft formation, and actin polymerisation dynamics, processes that drive cell invasion. This review discusses the relationship between well-studied cytoplasmic phosphoinositides and their lesser-known nuclear counterparts, highlighting their functional role in metastatic progression. Nuclear phosphoinositides, particularly PI(4,5)P2, are essential for regulating transcription factors and chromatin organisation, thereby shaping gene expression patterns. We also explore the role of PI(4,5)P2 and its metabolism in cancer cell invasiveness and metastasis, proposing a model in which the dysregulation of cytosolic and/or nuclear PI(4,5)P2 pool triggers malignant transformation. Understanding the PI(4,5)P2-related mechanisms underlying metastasis may provide insights into potential therapeutic targets, paving the way for more effective therapies and improved patient outcomes.
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