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Genotypes of the glutathione S-transferase superfamilydo not correlate with outcome of childhood acute lymphoblastic leukemia

机译:谷胱甘肽S-转移酶超家族的基因型与儿童急性淋巴细胞白血病的预后无关

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摘要

Several studies implicate GST polymorphisms in de novo cancer as well as cancers that are secondary to chemotherapy. In all cases, GST deficiency, rather than high GST activity, has been associated with an increased risk of cancer. However, because of its activity, GST has been associated with cancer-drug resistance, while GST deficiency of GSTT1 and GSTM1 could positively influence chemotherapeutic efficacy in some patients.1 In the case of childhood acute lymphoblastic leukemia (ALL), conflicting results have been reported on the associations between GSTM1 and GSTT1 genotypes and outcome.2,3 Stanulla et al.4 recently showed a two-fold and 2.8-fold reduction in risk of relapse, respectively, relative to the presence of the GSTM1 or GSTT1. These findings encouraged the evaluation of the GST genotypes contribution to therapeutic outcome in larger, well-characterized ALL patient populations prospectively enrolled in the same protocol treatment
机译:几项研究将GST多态性纳入了从头癌症以及化学疗法继发性癌症中。在所有情况下,GST不足而不是GST活性高都与癌症风险增加有关。然而,由于其活性,GST与癌症耐药性有关,而GSTT1和GSTM1的GST缺乏可对某些患者的化疗疗效产生积极影响。1在儿童急性淋巴细胞白血病(ALL)的情况下,出现了矛盾的结果。 [2,3] Stanulla等[4]最近显示,相对于GSTM1或GSTT1的存在,复发风险分别降低了2倍和2.8倍。这些发现鼓励评估GST基因型对预期参加同一方案治疗的更大,特征明确的所有ALL患者群体中治疗结果的贡献

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