FEBS Letters · 2007 · 113 citations · 19 references
Life SciencesOncologyPharmacologyCancer PharmacologyCell SignalingSignal TransductionCalcium SignalingCancer Cell SignalingCell Signaling NetworksCell Surface Receptor SignalingCell-surface ReceptorsIntracellular Calcium SignalingChemotactic InvasionChemotactic SignalingIntracellular Calcium ReleaseLuciferase Reporter AssaysLysophospholipid SignalingPhospholipase C PathwayPhospholipase C SignalingPhospholipase-mediated Signal Transduction
We investigated whether lysophosphatidylethanolamine (LPE) modulates cellular signaling in different cell types. SK-OV3 ovarian cancer cells and OVCAR-3 ovarian cancer cells were responsive to LPE. LPE-stimulated intracellular calcium concentration ([Ca(2+)](i)) increase was inhibited by U-73122, suggesting that LPE stimulates calcium signaling via phospholipase C activation. Moreover, pertussis toxin (PTX) almost completely inhibited [Ca(2+)](i) increase by LPE, indicating the involvement of PTX-sensitive G-proteins. Furthermore, we found that LPE stimulated chemotactic migration and cellular invasion in SK-OV3 ovarian cancer cells. We examined the role of lysophosphatidic acid receptors on LPE-stimulated cellular responses using HepG2 cells transfected with different LPA receptors, and found that LPE failed to stimulate nuclear factor kappa B-driven luciferase. We suggest that LPE stimulates a membrane bound receptor, different from well known LPA receptors, resulting in chemotactic migration and cellular invasion in SK-OV3 ovarian cancer cells.
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Ki16425, a Subtype-Selective Antagonist for EDG-Family Lysophosphatidic Acid Receptors
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Characterization of an ovarian cancer activating factor in ascites from ovarian cancer patients.
Yan Xu, Douglas C. Gaudette, Jessica Boynton et al. · PubMed · 1995 · 324 citations
Medicine, Biochemistry, Oncology +15
Lysophospholipids activate ovarian and breast cancer cells
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