Inositol-specific phospholipase C in low and fast proliferating hepatoma cell lines. (Articolo in rivista)

Type
Label
  • Inositol-specific phospholipase C in low and fast proliferating hepatoma cell lines. (Articolo in rivista) (literal)
Anno
  • 2003-01-01T00:00:00+01:00 (literal)
Alternative label
  • Santi P, Solimando L, Zini N, Santi S, Riccio M, Guidotti L (2003)
    Inositol-specific phospholipase C in low and fast proliferating hepatoma cell lines.
    in International journal of oncology
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Santi P, Solimando L, Zini N, Santi S, Riccio M, Guidotti L (literal)
Pagina inizio
  • 181 (literal)
Pagina fine
  • 188 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 22 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#note
  • I.F. 2,931 (literal)
Note
  • ISI Web of Science (WOS) (literal)
Titolo
  • Inositol-specific phospholipase C in low and fast proliferating hepatoma cell lines. (literal)
Abstract
  • Inositol lipid cycle, among the pletora of signalling events, is directly involved in cell growth. It is located both in the cytoplasm and in the nucleus. Disturbances may cause uncontrolled proliferation of the cell and ultimately cancer. The phosphatidyl inositol phospolipase C (PLC) is a key enzyme in the hydrolysis of polyphosphoinositides (PIs) and could be differently involved in the normal and pathological cell growth. We report immunochemical and immunocytochemical demonstrations that the PLC isoforms are present in both cytoplasmic and nuclear compartments of low and fast proliferating hepatoma cells. The PLC activity is increased in fast proliferating cells, in which PLC delta1 and to a greater extent PLC delta4 are more expressed at cytosolic level, suggesting an involvement of PI specific PLCs in the progression of cell cycle and in the control of cell proliferation and possibly of neoplastic cell growth. (literal)
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