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Vacuolar ATPase as a possible therapeutic target in human acute myeloid leukemia

Aasebø, Elise ; Bartaula-Brevik, Sushma ; Hernandez-Valladares, Maria ; Bruserud, Øystein

Expert Review of Hematology, 02 January 2018, Vol.11(1), pp.13-24 [Tạp chí có phản biện]

ISSN: 1747-4086 ; E-ISSN: 1747-4094 ; DOI: 10.1080/17474086.2018.1407239

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  • Nhan đề:
    Vacuolar ATPase as a possible therapeutic target in human acute myeloid leukemia
  • Tác giả: Aasebø, Elise ; Bartaula-Brevik, Sushma ; Hernandez-Valladares, Maria ; Bruserud, Øystein
  • Chủ đề: V-Atpase ; Acute Myeloid Leukemia ; Cytokine ; Chemokine ; Apoptosis
  • Là 1 phần của: Expert Review of Hematology, 02 January 2018, Vol.11(1), pp.13-24
  • Mô tả: Introduction: V-ATPase is a proton pump expressed both in the membrane of intracellular organelles (e.g. endosomes, lysosomes, Golgi structures) and the plasma membrane. It is an important regulator of organellar functions, intracellular molecular trafficking, intercellular communication and intracellular signaling. It is therefore considered as a possible therapeutic target in the treatment of human malignancies. Areas covered: Relevant publications were identified through literature searches in the PubMed database. We searched for original articles and reviews describing the possible importance of V-ATPase for leukemogenesis and chemosensitivity in human myeloid cells, especially acute myeloid leukemia (AML) cells. Expert commentary: The expression of V-ATPase in the primary human AML cells varies between patients, and high levels are associated with high constitutive release of a wide range of soluble mediators. Several of the molecules included in the V-ATPase interactome may also be important in leukemogenesis and/or development of chemoresistance in human AML. Therapeutic targeting of V-ATPase should therefore be regarded as a possible therapeutic strategy in human AML, but the efficiency of such targeting will probably differ between patients. The possibility of toxicity, especially hematological toxicity and immunosuppression, also has to be clarified.
  • Ngôn ngữ: English
  • Số nhận dạng: ISSN: 1747-4086 ; E-ISSN: 1747-4094 ; DOI: 10.1080/17474086.2018.1407239

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