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Title

Human acute myeloid leukemia cells express Neurokinin-1 receptor, which is involved in the antileukemic effect of Neurokinin-1 receptor antagonists

AuthorsMolinos-Quintana, A.; Trujillo-Hacha, P.; Piruat, José I.; Bejarano-García, José A.; García-Guerrero, Estefanía; Pérez-Simón, José A.; Muñoz Sáez, Miguel
KeywordsAcute myeloid leukemia
Neurokinin-1 receptor
Substance P (SP)
Xenograft, Aprepitant
Fosaprepitant
L-733,060
L-732,138, CP 96–345
Issue Date15-Feb-2019
PublisherSpringer Nature
CitationInvestigational New Drugs 37: 17-26 (2019)
AbstractThe substance P/neurokinin-1 receptor system has been implicated in tumor cell proliferation. Neurokinin-1 receptor has been identified in different solid tumors but not frequently in hematopoietic malignant cells. We investigated the presence of the Neurokinin-1 receptor in acute myeloid leukemia cell lines (KG-1 and HL-60), demonstrating that acute myeloid leukemia cell lines overexpress the truncated Neurokinin-1 receptor isoform compared with lymphocytes from healthy donors. Using the MTS (3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium) method, we demonstrated that substance P induced cell proliferation in both acute myeloid leukemia cell lines. We also observed that four different Neurokinin-1 receptor antagonists (L-733,060, L-732,138, CP 96–345 and aprepitant) elicited inhibition of acute myeloid leukemia cell growth lines in a concentration-dependent manner, while growth inhibition was only marginal in lymphocytes; the specific antitumor action of Neurokinin-1 receptor antagonists occurs via the Neurokinin-1 receptor, and leukemia cell death is due to apoptosis. Finally, administration of high doses of daily intraperitoneal fosaprepitant to NOD scid gamma mice previously xenografted with the HL60 cell line increased the median survival from 4 days (control group) to 7 days (treated group) (p = 0.059). Taken together, these findings suggest that Neurokinin-1 receptor antagonists suppress leukemic cell growth and may be considered to be potential antitumor drugs for the treatment of human acute myeloid leukemia.
Publisher version (URL)http://dx.doi.org/10.1007/s10637-018-0607-8
URIhttp://hdl.handle.net/10261/213857
Identifiersdoi: 10.1007/s10637-018-0607-8
e-issn: 1573-0646
issn: 0167-6997
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