Pregled bibliografske jedinice broj: 522964
Bone marrow stroma secreted cytokines protect JAK2V617F-mutated cells from the effects of a JAK2 Inhibitor
Bone marrow stroma secreted cytokines protect JAK2V617F-mutated cells from the effects of a JAK2 Inhibitor // Cancer research (Baltimore), 71 (2011), 11; 3831-3840 doi:10.1158/0008-5472.CAN-10-4002 (međunarodna recenzija, članak, znanstveni)
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Naslov
Bone marrow stroma secreted cytokines protect JAK2V617F-mutated cells from the effects of a JAK2 Inhibitor
Autori
Manshouri, Taghi ; Estrov, Zeev ; Quintás-Cardama, Alfonso ; Burger, Jan ; Zhang, Ying ; Livun, Ana ; Knez, Liza ; Harris, David ; Creighton, Chad J. ; Kantarjian, Hagop M. ; Verstovšek, Srđan
Izvornik
Cancer research (Baltimore) (0008-5472) 71
(2011), 11;
3831-3840
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
myeloproliferative neoplasms; JAK2(V617F); atiprimod; IL-6
Sažetak
Signals emanating from the bone marrow microenvironment, such as stromal cells, are thought to support the survival and proliferation of the malignant cells in patients with myeloproliferative neoplasms (MPN). To examine this hypothesis, we established a coculture platform [cells cocultured directly (cell-on-cell) or indirectly (separated by micropore membrane)] designed to interrogate the interplay between Janus activated kinase 2-V617F (JAK2(V617F))- positive cells and the stromal cells. Treatment with atiprimod, a potent JAK2 inhibitor, caused marked growth inhibition and apoptosis of human (SET-2) and mouse (FDCP-EpoR) JAK2(V617F)-positive cells as well as primary blood or bone marrow mononuclear cells from patients with polycythemia vera ; however, these effects were attenuated when any of these cell types were cocultured (cell-on- cell) with human marrow stromal cell lines (e.g., HS5, NK.tert, TM-R1). Coculture with stromal cells hampered the ability of atiprimod to inhibit phosphorylation of JAK2 and the downstream STAT3 and STAT5 pathways. This protective effect was maintained in noncontact coculture assays (JAK2(V617F)-positive cells separated by 0.4-μm- thick micropore membranes from stromal cells), indicating a paracrine effect. Cytokine profiling of supernatants from noncontact coculture assays detected distinctly high levels of interleukin 6 (IL-6), fibroblast growth factor (FGF), and chemokine C-X-C-motif ligand 10 (CXCL-10)/IFN-γ- inducible 10-kD protein (IP-10). Anti-IL-6, -FGF, or -CXCL-10/IP-10 neutralizing antibodies ablated the protective effect of stromal cells and restored atiprimod-induced apoptosis of JAK2(V617F)-positive cells. Therefore, our results indicate that humoral factors secreted by stromal cells protect MPN clones from JAK2 inhibitor therapy, thus underscoring the importance of targeting the marrow niche in MPN for therapeutic purposes.
Izvorni jezik
Engleski
Znanstvena područja
Biologija, Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
108-1980955-3094 - Genetika i funkcija hematopoeze i mikrookoliša Ph- mijeloproliferativnih bolesti (Kušec, Rajko, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Zagreb,
Klinička bolnica "Dubrava"
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE