INVESTIGADORES
MEDINA Vanina Araceli
artículos
Título:
Involvement of hydrogen peroxide in histamine-induced modulation of WM35
Autor/es:
VANINA MEDINA; NOELIA MASSARI; GRACIELA P CRICCO; GABRIELA A MARTÍN; ROSA M BERGOC; ELENA S RIVERA
Revista:
FREE RADICAL BIOLOGY AND MEDICINE
Editorial:
Elsevier Science
Referencias:
Año: 2009 vol. 46 p. 1510 - 1515
ISSN:
0891-5849
Resumen:
Histamine is a recognized growth factor in melanoma and exogenous histamine
produces a dual effect on proliferation. We have previously reported that histamine
at micromolar concentration reduces proliferation of melanoma cell lines. In order
to investigate the mechanism by which histamine inhibits proliferation of WM35
human melanoma cells, we have studied the involvement of histamine in reactive
oxygen species production and antioxidant enzymes regulation in these cells.
Results indicate that histamine treatment (10 uM) significantly increased hydrogen
peroxide levels, while it slightly decreased superoxide levels associated with an
enhancement of superoxide dismutase and a reduction of catalase activities.
Additionally, catalase treatment reversed the inhibitory effect of histamine on
proliferation and different treatments that reduce hydrogen peroxide formation
increased proliferation of these cells. Furthermore, we demonstrated that the
inhibition of proliferation produced by histamine was mediated at least in part by an
induction of cell senescence. We conclude that hydrogen peroxide is involved in
histamine-mediated modulation of proliferation in malignant melanoma cells
peroxide levels, while it slightly decreased superoxide levels associated with an
enhancement of superoxide dismutase and a reduction of catalase activities.
Additionally, catalase treatment reversed the inhibitory effect of histamine on
proliferation and different treatments that reduce hydrogen peroxide formation
increased proliferation of these cells. Furthermore, we demonstrated that the
inhibition of proliferation produced by histamine was mediated at least in part by an
induction of cell senescence. We conclude that hydrogen peroxide is involved in
histamine-mediated modulation of proliferation in malignant melanoma cells
peroxide levels, while it slightly decreased superoxide levels associated with an
enhancement of superoxide dismutase and a reduction of catalase activities.
Additionally, catalase treatment reversed the inhibitory effect of histamine on
proliferation and different treatments that reduce hydrogen peroxide formation
increased proliferation of these cells. Furthermore, we demonstrated that the
inhibition of proliferation produced by histamine was mediated at least in part by an
induction of cell senescence. We conclude that hydrogen peroxide is involved in
histamine-mediated modulation of proliferation in malignant melanoma cells
peroxide levels, while it slightly decreased superoxide levels associated with an
enhancement of superoxide dismutase and a reduction of catalase activities.
Additionally, catalase treatment reversed the inhibitory effect of histamine on
proliferation and different treatments that reduce hydrogen peroxide formation
increased proliferation of these cells. Furthermore, we demonstrated that the
inhibition of proliferation produced by histamine was mediated at least in part by an
induction of cell senescence. We conclude that hydrogen peroxide is involved in
histamine-mediated modulation of proliferation in malignant melanoma cells
peroxide levels, while it slightly decreased superoxide levels associated with an
enhancement of superoxide dismutase and a reduction of catalase activities.
Additionally, catalase treatment reversed the inhibitory effect of histamine on
proliferation and different treatments that reduce hydrogen peroxide formation
increased proliferation of these cells. Furthermore, we demonstrated that the
inhibition of proliferation produced by histamine was mediated at least in part by an
induction of cell senescence. We conclude that hydrogen peroxide is involved in
histamine-mediated modulation of proliferation in malignant melanoma cells
peroxide levels, while it slightly decreased superoxide levels associated with an
enhancement of superoxide dismutase and a reduction of catalase activities.
Additionally, catalase treatment reversed the inhibitory effect of histamine on
proliferation and different treatments that reduce hydrogen peroxide formation
increased proliferation of these cells. Furthermore, we demonstrated that the
inhibition of proliferation produced by histamine was mediated at least in part by an
induction of cell senescence. We conclude that hydrogen peroxide is involved in
histamine-mediated modulation of proliferation in malignant melanoma cells
peroxide levels, while it slightly decreased superoxide levels associated with an
enhancement of superoxide dismutase and a reduction of catalase activities.
Additionally, catalase treatment reversed the inhibitory effect of histamine on
proliferation and different treatments that reduce hydrogen peroxide formation
increased proliferation of these cells. Furthermore, we demonstrated that the
inhibition of proliferation produced by histamine was mediated at least in part by an
induction of cell senescence. We conclude that hydrogen peroxide is involved in
histamine-mediated modulation of proliferation in malignant melanoma cells
peroxide levels, while it slightly decreased superoxide levels associated with an
enhancement of superoxide dismutase and a reduction of catalase activities.
Additionally, catalase treatment reversed the inhibitory effect of histamine on
proliferation and different treatments that reduce hydrogen peroxide formation
increased proliferation of these cells. Furthermore, we demonstrated that the
inhibition of proliferation produced by histamine was mediated at least in part by an
induction of cell senescence. We conclude that hydrogen peroxide is involved in
histamine-mediated modulation of proliferation in malignant melanoma cells
peroxide levels, while it slightly decreased superoxide levels associated with an
enhancement of superoxide dismutase and a reduction of catalase activities.
Additionally, catalase treatment reversed the inhibitory effect of histamine on
proliferation and different treatments that reduce hydrogen peroxide formation
increased proliferation of these cells. Furthermore, we demonstrated that the
inhibition of proliferation produced by histamine was mediated at least in part by an
induction of cell senescence. We conclude that hydrogen peroxide is involved in
histamine-mediated modulation of proliferation in malignant melanoma cells
M) significantly increased hydrogen
peroxide levels, while it slightly decreased superoxide levels associated with an
enhancement of superoxide dismutase and a reduction of catalase activities.
Additionally, catalase treatment reversed the inhibitory effect of histamine on
proliferation and different treatments that reduce hydrogen peroxide formation
increased proliferation of these cells. Furthermore, we demonstrated that the
inhibition of proliferation produced by histamine was mediated at least in part by an
induction of cell senescence. We conclude that hydrogen peroxide is involved in
histamine-mediated modulation of proliferation in malignant melanoma cells