四川大学学报（医学版）2017，Vol.48Issue(3)：389-393,5.
Glut5在Ph+急性淋巴细胞白血病伊马替尼耐药中的机制研究
The Roles of Glut5 in Imatinib Resistance in the Ph+ Acute Lymphoblastic Leukemia Cell
摘要
Abstract
Objective To explore the possible roles of glucose transport 5 (Glut5) in imatinib resistance in the Ph+ acute lymphoblastic leukemia cell (Ph+ ALL).Methods The gene chip technique was used to detect different gene expression between Ph+ ALL cell line SUP-B15/R (imatinib resistant cell line) and SUP-B15/S (imatinib sensitive cell line),the gene of solute carrier family 2 member 5 (SLC2A5) and its coded protein Glut5 were screened out and were reconfirmed by qPCR and Western blot assay.The imatinib half maximal inhibitory concentration (ICs0) to SUP-B15/S cells with or without fructose treatment was further detected by MTT assay,simultaneously signal pathway gene was detected by qPCR assay.Results Metabolism related gene SLC2A5 was screened out with gene chip technique and the Western blot assay and qPCR confirmed the high expression of SLC2A5 gene and its coded protein Glut5 in SUP-B15/R cells.IC50 values of imatinib to SUP-B15/S cells after treatment with 25 μmol/L fructose were increased from (44.50±2.38) μmol/L to (64.71 ± 1.69) μmol/L,in the meanwhile,PI3K and AKT mRNA level also increased in fructose treated SUP-B15/S cells compared to the control.Conclusions High expression of SLC2A5 and Glut5 protein in SUP-B15/R cells leads to increased fructose absorption,and further activates PI3K/AKT pathway which cause the SUP-B15 cell resistance to imatinib.关键词
Ph+急性淋巴细胞白血病/伊马替尼耐药/葡萄糖转运体5/果糖Key words
Ph+ acute lymphoblastic leukemia/Imatinib resistance/Glucose transport 5/Fructose引用本文复制引用
严天友,娜仁朵兰,龚玉萍..Glut5在Ph+急性淋巴细胞白血病伊马替尼耐药中的机制研究[J].四川大学学报（医学版）,2017,48(3):389-393,5.基金项目
四川省中医药管理局项目(No.2014A038)和四川省科技厅基金项目(No.2015SZ0234-5)资助 （No.2014A038）
