Bonati A, Rizzoli V, Lunghi P
Department of Clinical Sciences, University of Parma, Italy.
Curr Pharm Biotechnol. 2006 Dec;7(6):397-405. doi: 10.2174/138920106779116829.
Currently, Arsenic Trioxide (ATO) is considered the treatment of choice for patients with relapsed acute promyelocytic leukemia (APL). Recently, a durable remission with minimal toxicity by single agent ATO or ATO + ATRA in newly diagnosed APL was reported by different groups. These regimens have minimal toxicity and can be administered on an outpatient basis after remission induction, thus they could become a real, less toxic and more economic option to ATRA + anthracyclines in particular in low risk APL, or in patients that cannot undergo chemotherapy because of age or comorbid conditions and in patients that refuse chemotherapy. Significantly, these therapies are a successful attempt to cure a tumoral disease without chemotherapy. The results of clinical trials of ATO administration as single agent in multiple myeloma (MM) and myelodisplastic syndromes (MDS) were encouraging and showed clinical effects but they were not close to APL success. On the contrary, results of clinical trials to treat non-APL acute myeloid leukemia (AML) were disappointing. We suggest that a combination therapy with drugs targeting specific pro-survival molecules or capable to enhance pro-apoptotic pathways may lead to an improvement of ATO efficacy against hematological malignancies, in particular AML. Our pre-clinical studies showed that ATO is capable to induce cell death in acute leukemia cells but the apoptotic function is limited since it can induce also a mechanism of cell defense by activating pro-survival molecules such as MEK-ERK, Bcl-xL, Bcl-2. By combining ATO with specific MEK inhibitors, we demonstrated that the block of MEK-ERK phosphorylation, the induction of Bad de-phosphorylation, and activation of p53AIP1 apoptotic pathway interrupt the pro-survival mechanisms of ATO and kill the leukemic cells by apoptotic synergism. Our results provide an experimental basis for combined or sequential treatment with MEK inhibitors and ATO in AML. The renaissance of ATO as a drug in moderne medicine may be considered, together with ATRA success, a victory of empirical analysis, that had (and has) great impact on Chinese culture.
目前,三氧化二砷(ATO)被认为是复发急性早幼粒细胞白血病(APL)患者的首选治疗方法。最近,不同研究团队报告了单药ATO或ATO + 全反式维甲酸(ATRA)治疗新诊断APL患者可实现持久缓解且毒性极小。这些方案毒性极小,缓解诱导后可门诊给药,因此它们可能成为一种真正的、毒性更小且更经济的选择,尤其适用于低危APL患者,或因年龄或合并症无法接受化疗的患者以及拒绝化疗的患者。值得注意的是,这些疗法是在不进行化疗的情况下治愈肿瘤疾病的成功尝试。ATO作为单药用于多发性骨髓瘤(MM)和骨髓增生异常综合征(MDS)的临床试验结果令人鼓舞,并显示出临床疗效,但尚未达到APL治疗的成功程度。相反,治疗非APL急性髓系白血病(AML)的临床试验结果令人失望。我们认为,联合使用靶向特定促生存分子或能够增强促凋亡途径的药物进行治疗,可能会提高ATO对血液系统恶性肿瘤,尤其是AML的疗效。我们的临床前研究表明,ATO能够诱导急性白血病细胞死亡,但凋亡功能有限,因为它还可通过激活MEK-ERK、Bcl-xL、Bcl-2等促生存分子诱导细胞防御机制。通过将ATO与特定的MEK抑制剂联合使用,我们证明阻断MEK-ERK磷酸化、诱导Bad去磷酸化以及激活p53AIP1凋亡途径可中断ATO的促生存机制,并通过凋亡协同作用杀死白血病细胞。我们的研究结果为AML中MEK抑制剂与ATO联合或序贯治疗提供了实验依据。ATO作为一种药物在现代医学中的复兴,连同ATRA的成功,可被视为经验分析的胜利,这对中国文化产生了(并仍在产生)巨大影响。