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Sphingosine kinase 1 participates in the activation, proliferation and survival of chronic lymphocytic leukemia cells.

作者信息

Almejún María Belén, Borge Mercedes, Colado Ana, Elías Esteban Enrique, Podaza Enrique, Risnik Denise, De Brasi Carlos Daniel, Stanganelli Carmen, Slavutsky Irma, Cabrejo María, Fernández-Grecco Horacio, Bezares Raimundo Fernando, Cranco Santiago, Burgos Rubén Ángel, Sánchez-Ávalos Julio César, Oppezzo Pablo, Giordano Mirta, Gamberale Romina

机构信息

Laboratorio de Inmunología Oncológica, Instituto de Medicina Experimental (IMEX)-CONICET-Academia Nacional de Medicina (ANM), Buenos Aires, Argentina.

Departamento de Fisiología, Biología Molecular y Celular, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Argentina.

出版信息

Haematologica. 2017 Jul;102(7):e257-e260. doi: 10.3324/haematol.2017.167353. Epub 2017 Mar 30.

DOI:10.3324/haematol.2017.167353
PMID:28360148
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5566050/
Abstract
摘要

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本文引用的文献

1
Sphingosine-1 Phosphate: A New Modulator of Immune Plasticity in the Tumor Microenvironment.鞘氨醇-1-磷酸:肿瘤微环境中免疫可塑性的新型调节剂。
Front Oncol. 2016 Oct 17;6:218. doi: 10.3389/fonc.2016.00218. eCollection 2016.
2
The Sphingosine-1-Phosphate Modulator FTY720 Targets Multiple Myeloma via the CXCR4/CXCL12 Pathway.鞘氨醇-1-磷酸调节剂 FTY720 通过 CXCR4/CXCL12 途径靶向多发性骨髓瘤。
Clin Cancer Res. 2017 Apr 1;23(7):1733-1747. doi: 10.1158/1078-0432.CCR-15-2618. Epub 2016 Oct 3.
3
Therapeutic potential of targeting sphingosine kinases and sphingosine 1-phosphate in hematological malignancies.靶向鞘氨醇激酶和鞘氨醇 1-磷酸在血液系统恶性肿瘤中的治疗潜力。
Leukemia. 2016 Nov;30(11):2142-2151. doi: 10.1038/leu.2016.208. Epub 2016 Jul 27.
4
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Br J Haematol. 2017 Jul;178(1):155-158. doi: 10.1111/bjh.14119. Epub 2016 May 25.
5
Lysosomotropic agents selectively target chronic lymphocytic leukemia cells due to altered sphingolipid metabolism.溶酶体靶向药物由于鞘脂代谢改变而选择性地靶向慢性淋巴细胞白血病细胞。
Leukemia. 2016 Jun;30(6):1290-300. doi: 10.1038/leu.2016.4. Epub 2015 Feb 23.
6
Sphingosine kinase inhibitors decrease viability and induce cell death in natural killer-large granular lymphocyte leukemia.鞘氨醇激酶抑制剂可降低自然杀伤大颗粒淋巴细胞白血病的细胞活力并诱导细胞死亡。
Cancer Biol Ther. 2015;16(12):1830-40. doi: 10.1080/15384047.2015.1078949.
7
SphK1 inhibitor II (SKI-II) inhibits acute myelogenous leukemia cell growth in vitro and in vivo.鞘氨醇激酶1抑制剂II(SKI-II)在体外和体内均能抑制急性髓性白血病细胞的生长。
Biochem Biophys Res Commun. 2015 May 15;460(4):903-8. doi: 10.1016/j.bbrc.2015.03.114. Epub 2015 Mar 28.
8
Revisiting the sphingolipid rheostat: Evolving concepts in cancer therapy.重新审视鞘脂变阻器:癌症治疗中的不断演变的概念。
Exp Cell Res. 2015 May 1;333(2):195-200. doi: 10.1016/j.yexcr.2015.02.025. Epub 2015 Mar 11.
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A sphingosine kinase-1 inhibitor, SKI-II, induces growth inhibition and apoptosis in human gastric cancer cells.一种鞘氨醇激酶-1抑制剂SKI-II可诱导人胃癌细胞生长抑制和凋亡。
Asian Pac J Cancer Prev. 2014;15(23):10381-5. doi: 10.7314/apjcp.2014.15.23.10381.
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The expression of sphingosine-1 phosphate receptor-1 in chronic lymphocytic leukemia cells is impaired by tumor microenvironmental signals and enhanced by piceatannol and R406.慢性淋巴细胞白血病细胞中鞘氨醇-1-磷酸受体-1的表达受到肿瘤微环境信号的损害,并被白皮杉醇和R406增强。
J Immunol. 2014 Sep 15;193(6):3165-74. doi: 10.4049/jimmunol.1400547. Epub 2014 Aug 15.