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首页> 外文期刊>Japanese Journal of Cancer Research >Effects of 1-methyl-3-propyl-7-butylxanthine (MPBX) on idarubicin-induced antitumor activity and bone marrow suppression.
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Effects of 1-methyl-3-propyl-7-butylxanthine (MPBX) on idarubicin-induced antitumor activity and bone marrow suppression.

机译:1-甲基-3-丙基-7-丁基黄嘌呤(MPBX)对伊达比星诱导的抗肿瘤活性和骨髓抑制的影响。

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摘要

The effects of 1-methyl-3-propyl-7-butylxanthine (MPBX), a xanthine derivative, on idarubicin (IDA)-induced antitumor activity against P388 leukemia cells (P388) and bone marrow suppression were examined. In P388 tumor-bearing mice, the combination of MPBX with IDA increased the antitumor activity of IDA. The IDA concentration in the tumors in the MPBX combination group increased by 2.0-fold compared to the level in the IDA-alone group. On the other hand, as regards IDA-induced bone marrow suppression, the combination of MPBX with IDA reduced the decrease in the bone marrow cell number by 30% compared to that in the IDA-alone group. In addition, the IDA concentration in the bone marrow cells was decreased by the combination of MPBX with IDA. An in vitro experiment showed that MPBX facilitated IDA influx and suppressed IDA efflux in P388 cells. In conclusion, the combination of MPBX with IDA increased the antitumor activity and decreased the bone marrow suppression. Therefore, we expect that the combination of MPBX with IDA will be useful for leukemia chemotherapy.
机译:检验了黄嘌呤衍生物1-甲基-3-丙基-7-丁基黄嘌呤(MPBX)对伊达比星(IDA)诱导的针对P388白血病细胞(P388)的抗肿瘤活性和骨髓抑制的影响。在带有P388的荷瘤小鼠中,MPBX与IDA的组合增加了IDA的抗肿瘤活性。与单独使用IDA的组相比,MPBX组合组的肿瘤中的IDA浓度增加了2.0倍。另一方面,关于IDA诱导的骨髓抑制,与单独使用IDA的组相比,MPBX与IDA的组合使骨髓细胞数的减少减少了30%。此外,MPBX与IDA的组合可降低骨髓细胞中IDA的浓度。体外实验表明,MPBX促进IDA流入并抑制ID388在P388细胞中的流出。总之,MPBX与IDA的组合可提高抗肿瘤活性并降低骨髓抑制作用。因此,我们预期MPBX与IDA的组合将对白血病化疗有用。

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