TY - JOUR
T1 - Blocking the APRIL circuit enhances acute myeloid leukemia cell chemosensitivity
AU - Bonci, Désirée
AU - Musumeci, Maria
AU - Coppola, Valeria
AU - Addario, Antonio
AU - Conticello, Concetta
AU - Hahne, Michael
AU - Gulisano, Massimo
AU - Grignani, Francesco
AU - De Maria Marchiano, Ruggero
PY - 2008
Y1 - 2008
N2 - Resistance to chemotherapy-induced cell death represents a major obstacle in the treatment of acute myeloid leukemia. APRIL (A Proliferation Inducing Ligand) is a member of the tumor necrosis factor superfamily that plays a key role in normal B-cell development, while promoting survival and proliferation of malignant B cells. We investigated APRIL expression and activity in acute myeloid leukemia. We found that APRIL mRNA and protein, including the secreted form, are expressed in leukemic cells of patients with M0, M2 and M4 acute myeloid leukemia subtypes but not in normal hematopoietic progenitors. Retrovirus-mediated APRIL expression in normal hematopoietic progenitors confers resistance to chemotherapeutic drugs-induced apoptosis. Conversely, blocking APRIL function by recombinant soluble APRIL receptors increased chemotherapeutic drugs-induced cell adeath in acute myeloid leukemia cells. These results indicate that APRIL acts in an autocrine fashion to protect acute myeloid leukemia cells from drug-induced death and foresee a therapeutic potential of APRIL antagonists in the treatment of acute myeloid leukemia. ©2008 Ferrata Storti Foundation.
AB - Resistance to chemotherapy-induced cell death represents a major obstacle in the treatment of acute myeloid leukemia. APRIL (A Proliferation Inducing Ligand) is a member of the tumor necrosis factor superfamily that plays a key role in normal B-cell development, while promoting survival and proliferation of malignant B cells. We investigated APRIL expression and activity in acute myeloid leukemia. We found that APRIL mRNA and protein, including the secreted form, are expressed in leukemic cells of patients with M0, M2 and M4 acute myeloid leukemia subtypes but not in normal hematopoietic progenitors. Retrovirus-mediated APRIL expression in normal hematopoietic progenitors confers resistance to chemotherapeutic drugs-induced apoptosis. Conversely, blocking APRIL function by recombinant soluble APRIL receptors increased chemotherapeutic drugs-induced cell adeath in acute myeloid leukemia cells. These results indicate that APRIL acts in an autocrine fashion to protect acute myeloid leukemia cells from drug-induced death and foresee a therapeutic potential of APRIL antagonists in the treatment of acute myeloid leukemia. ©2008 Ferrata Storti Foundation.
KW - APRIL
KW - Acute myeloid leukemia
KW - Antineoplastic Agents
KW - Autocrine Communication
KW - Chemosensitivity
KW - Drug Resistance, Neoplasm
KW - Hematology
KW - Humans
KW - Leukemia, Myeloid, Acute
KW - Tumor Cells, Cultured
KW - Tumor Necrosis Factor Ligand Superfamily Member 13
KW - APRIL
KW - Acute myeloid leukemia
KW - Antineoplastic Agents
KW - Autocrine Communication
KW - Chemosensitivity
KW - Drug Resistance, Neoplasm
KW - Hematology
KW - Humans
KW - Leukemia, Myeloid, Acute
KW - Tumor Cells, Cultured
KW - Tumor Necrosis Factor Ligand Superfamily Member 13
UR - http://hdl.handle.net/10807/112985
UR - http://www.haematologica.org/cgi/reprint/93/12/1899
U2 - 10.3324/haematol.13035
DO - 10.3324/haematol.13035
M3 - Article
SN - 0390-6078
VL - 93
SP - 1899
EP - 1902
JO - Haematologica
JF - Haematologica
ER -