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Anti-Leukemic Properties of Histamine in Monocytic Leukemia: The Role of NOX2

Kiffin, Roberta (author)
Gothenburg University,Göteborgs universitet,Sahlgrenska Cancer Center
Grauers Wiktorin, Hanna, 1990 (author)
Gothenburg University,Göteborgs universitet,Sahlgrenska Cancer Center
Nilsson, Malin S. (author)
Gothenburg University,Göteborgs universitet,Sahlgrenska Cancer Center
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Aurelius, Johan, 1980 (author)
Gothenburg University,Göteborgs universitet,Sahlgrenska Cancer Center
Aydin, Ebru (author)
Gothenburg University,Göteborgs universitet,Sahlgrenska Cancer Center
Lenox, Brianna (author)
Gothenburg University,Göteborgs universitet,Sahlgrenska Cancer Center
Nilsson, Jonas A, 1971 (author)
Gothenburg University,Göteborgs universitet,Sahlgrenska Cancer Center
Ståhlberg, Anders, 1975 (author)
Gothenburg University,Göteborgs universitet,Sahlgrenska Cancer Center
Bergh Thorén, Fredrik, 1976 (author)
Gothenburg University,Göteborgs universitet,Sahlgrenska Cancer Center
Hellstrand, Kristoffer, 1956 (author)
Gothenburg University,Göteborgs universitet,Sahlgrenska Cancer Center
Martner, Anna, 1979 (author)
Gothenburg University,Göteborgs universitet,Sahlgrenska Cancer Center
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 (creator_code:org_t)
2018-06-18
2018
English.
In: Frontiers in Oncology. - : Frontiers Media SA. - 2234-943X. ; 8
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • In patients with acute myeloid leukemia (AML), treatment with histamine dihydrochloride (HDC) and low-dose IL-2 (HDC/ IL-2) in the post-chemotherapy phase has been shown to reduce the incidence of leukemic relapse. The clinical benefit of HDC/ IL-2 is pronounced in monocytic forms of AML, where the leukemic cells express histamine type 2 receptors (H2R) and the NAPDH oxidase-2 (NOX2). HDC ligates to H(2)Rs to inhibit NOX2-derived formation of reactive oxygen species, but details regarding the anti-leukemic actions of HDC remain to be elucidated. Here, we report that human NOX2(+) myelomonocytic/monocytic AML cell lines showed increased expression of maturation markers along with reduced leukemic cell proliferation after exposure to HDC in vitro. These effects of HDC were absent in corresponding leukemic cells genetically depleted of NOX2 (NOX2(-/-)). We also observed that exposure to HDC altered the expression of genes involved in differentiation and cell cycle progression in AML cells and that these effects required the presence of NOX2. HDC promoted the differentiation also of primary monocytic, but not non-monocytic, AML cells in vitro. In a xenograft model, immunodeficient NOG mice were inoculated with wild-type or NOX2(-/-) human monocytic AML cells and treated with HDC in vivo. The administration of HDC reduced the in vivo expansion of NOX2(+/+), but not of NOX2(-/-) human monocytic AML cells. We propose that NOX2 may be a conceivable target in the treatment of monocytic AML.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Keyword

histamine
NAPDH oxidase
NOX2
acute myeloid leukemia
acute monocytic leukemia
acute myelomonocytic leukemia
acute myeloid-leukemia
reactive oxygen metabolites
low-dose
interleukin-2
nadph-oxidase activity
cell-line
remission maintenance
human neutrophils
nk cells
expression
differentiation
Oncology

Publication and Content Type

ref (subject category)
art (subject category)

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