Expression of functional neuronal receptor latrophilin 1 in human acute myeloid leukaemia cells

被引:13
|
作者
Sumbayev, Vadim V. [1 ]
Silva, Isabel Goncalves [1 ]
Blackburn, Jennifer [1 ]
Gibbs, Bernhard F. [1 ]
Yasinska, Inna M. [1 ]
Garrett, Michelle D. [2 ]
Tonevitsky, Alexander G. [3 ]
Ushkaryov, Yuri A. [1 ]
机构
[1] Univ Kent, Sch Pharm, Chatham ME4 4TB, Kent, England
[2] Univ Kent, Sch Biosci, Canterbury CT2 7NJ, Kent, England
[3] Minist Hlth Russian Federat, Branch Natl Med Res Radiol Ctr, Hertsen Moscow Oncol Res Inst, Moscow 125284, Russia
基金
俄罗斯科学基金会;
关键词
latrophilin; myeloid leukaemia; mammalian target of rapamycin; BONE-MARROW; PATHWAY; LTXN4C; TIM-3; FORM;
D O I
10.18632/oncotarget.10039
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Acute myeloid leukaemia (AML) is a blood cancer affecting cells of myeloid lineage. It is characterised by rapid growth of malignant leukocytes that accumulate in the bone marrow and suppress normal haematopoiesis. This systemic disease remains a serious medical burden worldwide. Characterisation of protein antigens specifically expressed by malignant cells, but not by healthy leukocytes, is vital for the diagnostics and targeted treatment of AML. Here we report, for the first time, that the neuronal receptor latrophilin-1 is expressed in human monocytic leukaemia cell lines and in primary human AML cells. However, it is absent in healthy leukocytes. Latrophilin-1 is functional in leukaemia cells tested, and its biosynthesis is controlled through the mammalian target of rapamycin (mTOR), a master regulator of myeloid cell translational pathways. Our findings demonstrate that latrophilin-1 could be considered as a novel biomarker of human AML, which offers potential new avenues for AML diagnosis and treatment.
引用
收藏
页码:45575 / 45583
页数:9
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