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CD56 and RUNX1 isoforms in AML prognosis and their therapeutic potential

机译:CD56和RUNX1亚型在AML预后中的治疗潜力

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Neural cell adhesion molecule (NCAM/CD56) expression in acute myeloid leukemia (AML) has been associated with extramedullary leukemia, multidrug resistance, shorter remission and survival. Recently, Bloomfield et al. published a succinct review of issues surrounding the AML prognostication and current therapeutics. However, we want to reiterate the prognostic value and therapeutic potential of CD56 that is frequently expressed in AML as was also reported by their own group earlier. In addition, novel RUNX1 isoforms contribute in controlling CD56 expression in AML cells. Anti-CD56 antibody therapy deserves exploration as an arsenal against AML patients expressing CD56. Relevantly, targeting RNA splicing machinery or RUNX1 isoform-specific siRNA may also become part of future therapeutic strategies for AML with CD56 overexpression.
机译:急性髓细胞性白血病(AML)中神经细胞粘附分子(NCAM / CD56)的表达与髓外白血病,多药耐药性,缓解期和生存期短有关。最近,Bloomfield等人。发表了有关AML预后和当前治疗方法的简要综述。但是,我们想重申CD56在AML中经常表达的预后价值和治疗潜力,正如他们自己的研究小组先前所报道的那样。此外,新型RUNX1亚型有助于控制AML细胞中的CD56表达。抗CD56抗体疗法作为针对表达CD56的AML患者的武器库值得探索。与此相关,靶向RNA剪接机制或RUNX1亚型特异性siRNA也可能成为CD56过表达的AML未来治疗策略的一部分。

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