Roles of hsa-miR-12462 and SLC9A1 in acute myeloid leukemia.
Yan JiaWei LiuHui-En ZhanXiao-Ping YiHui LiangQi-Li ZhengXin-Ya JiangHai-Yan ZhouLiang ZhaoXie-Lan ZhaoHui ZengPublished in: Journal of hematology & oncology (2020)
MicroRNAs (miRNAs) play important roles in cell proliferation, differentiation, and survival and may be useful for acute myeloid leukemia (AML) diagnosis and prognosis. In this study, we defined a novel miRNA, hsa-miR-12462, through small RNA sequencing of the bone marrow (BM) cells from 128 AML patients. Overexpression of hsa-miR-12462 in AML cells (U937 and HL-60) significantly decreased their growth rate when compared with those of the wild-type and MOCK controls. In a xenograft mouse model, tumor weight and size in the mice bearing the U937 cells with hsa-miR-12462 overexpression were significantly reduced when compared with those bearing the mock cells. The AML cells overexpressing hsa-miR-12462 had increased sensitivity to cytarabine chemotherapy. Combining the data from the MiRDB, an online microRNA database ( http://mirdb.org ), with the RNA-sequencing results, SLC9A1 was predicted to be one of the targets of hsa-miR-12462. hsa-miR-12462 was further confirmed to bind exclusively to the 3'UTR of SLC9A1 in U937 cells, leading to downregulation of SLC9A1. In summary, a higher level of hsa-miR-12462 in AML cells is associated with increased sensitivity to cytarabine chemotherapy via downregulation of SLC9A1.
Keyphrases
- cell proliferation
- acute myeloid leukemia
- induced apoptosis
- long non coding rna
- cell cycle arrest
- long noncoding rna
- bone marrow
- pi k akt
- endoplasmic reticulum stress
- mouse model
- emergency department
- oxidative stress
- radiation therapy
- machine learning
- single cell
- end stage renal disease
- chronic kidney disease
- mesenchymal stem cells
- ejection fraction
- body mass index
- acute lymphoblastic leukemia
- wild type
- adipose tissue
- transcription factor
- electronic health record
- body weight