Hu Wen-Jia, Sun Yu-Jie
Department of Cell Biology, Nanjing Medical University, Nanjing 210029, China.
Yi Chuan. 2012 Jun;34(6):705-10. doi: 10.3724/sp.j.1005.2012.00705.
Folylpolyglutamate synthetase (FPGS) is the key enzyme that converts chemotherapy drug Methotrexate (MTX) into MTXPG. The expression level of FPGS directly influences MTX-sensitivity of tumor cells. Compared with B-cell acute lymphocytic leukemia (B-ALL), T-cell acute lymphocytic leukemia (T-ALL) cells express a lower level of FPGS, which results in insensitivity of the cells to MTX. Our previous work has demonstrated that 279 bp mbr element located within the 3'-UTR of the BCL2 gene possesses enhancer function. In this study, FPGS expression plasmid containing mbr element at the 5' upstream of the gene was constructed and transfected into Jurkat cells to sensitize the cells to MTX. Western blotting and MTT assay were applied to detect the FPGS expression level and suppression rate of the cells treated by MTX, respectively. We found that the mbr enhanced the expression of FPGS significantly and increased sensitivity of Jurkat cells to MTX efficiently, while FPGS expression plasmid without mbr element had less effect. Our data provides a new clue for the clinical application of mbr regulatory element and may contribute to improvement of MTX treatment in T-ALL.
叶酸多聚谷氨酸合成酶(FPGS)是将化疗药物甲氨蝶呤(MTX)转化为MTXPG的关键酶。FPGS的表达水平直接影响肿瘤细胞对MTX的敏感性。与B细胞急性淋巴细胞白血病(B-ALL)相比,T细胞急性淋巴细胞白血病(T-ALL)细胞中FPGS的表达水平较低,这导致细胞对MTX不敏感。我们之前的研究表明,位于BCL2基因3'-UTR内的279 bp mbr元件具有增强子功能。在本研究中,构建了在基因5'上游含有mbr元件的FPGS表达质粒,并将其转染到Jurkat细胞中,以使细胞对MTX敏感。分别应用蛋白质免疫印迹法和MTT法检测MTX处理后细胞的FPGS表达水平和抑制率。我们发现,mbr显著增强了FPGS的表达,并有效提高了Jurkat细胞对MTX的敏感性,而不含mbr元件的FPGS表达质粒作用较小。我们的数据为mbr调控元件的临床应用提供了新线索,并可能有助于改善T-ALL的MTX治疗效果。