School of Medicine, Deakin University, Pigdon Road, Waurn Ponds, Geelong, Victoria 3217, Australia.
Br J Haematol. 2011 Oct;155(1):3-13. doi: 10.1111/j.1365-2141.2011.08807.x. Epub 2011 Aug 2.
Haematological malignancies result from a heterogeneous mix of genetic mutations and chromosome aberrations and translocations. Targeted therapies, such as the anti-CD20 antibody rituximab, or the BCR-ABL1 inhibitor imatinib, have proven to be effective treatments in the management of some of these malignancies, though relapsing or refractory disease is still common. Nucleic acid-based therapies have also entered the clinical arena, providing an alternative, complementary approach. The forerunner of these therapies were the antisense oligonucleotides, but their scope has expanded to include short-interfering RNA (siRNA), microRNA, decoy oligonucleotides and aptamers. These can be used either as mono-therapeutics, in conjunction with current chemotherapy regimens, or in combination with each other to improve therapeutic efficacy. Not only can these nucleic acid-based therapies silence target genes, they also have the potential of restoring gene function. While challenges remain in delivering effective doses of nucleic acid in vivo, these are steadily being met, suggesting an optimistic future in the treatment of haematological malignancies. This review summarizes the application of nucleic acid-based therapeutics, particularly aptamers, in the diagnosis and treatment of haematological malignancies.
血液系统恶性肿瘤是由遗传突变和染色体异常及易位引起的异质性混合。靶向治疗,如抗 CD20 抗体利妥昔单抗或 BCR-ABL1 抑制剂伊马替尼,已被证明对这些恶性肿瘤的某些治疗有效,尽管复发或难治性疾病仍很常见。核酸治疗也已进入临床领域,提供了一种替代的、互补的方法。这些治疗方法的先驱是反义寡核苷酸,但它们的范围已经扩大到包括小干扰 RNA(siRNA)、microRNA、诱饵寡核苷酸和适体。这些可以单独用作单一疗法,与当前的化疗方案联合使用,也可以与其他疗法联合使用以提高治疗效果。这些核酸治疗不仅可以沉默靶基因,还有可能恢复基因功能。虽然在体内有效递送核酸方面仍存在挑战,但这些挑战正在得到解决,这表明在血液系统恶性肿瘤的治疗方面有着乐观的未来。本综述总结了核酸治疗,特别是适体,在血液系统恶性肿瘤的诊断和治疗中的应用。