Bhatla Teena, Jones Courtney L, Meyer Julia A, Vitanza Nicholas A, Raetz Elizabeth A, Carroll William L
Division of Pediatric Hematology-Oncology, New York University Cancer Institute, New York University Langone Medical Center, New York, NY.
J Pediatr Hematol Oncol. 2014 Aug;36(6):413-8. doi: 10.1097/MPH.0000000000000179.
Although great strides have been made in the improvement of outcome for newly diagnosed pediatric acute lymphoblastic leukemia because of refinements in risk stratification and selective intensification of therapy, the prognosis for relapsed leukemia has lagged behind significantly. Understanding the underlying biological pathways responsible for drug resistance is essential to develop novel approaches for the prevention of recurrence and treatment of relapsed disease. High throughput genomic technologies have the potential to revolutionize cancer care in this era of personalized medicine. Using such advanced technologies, we and others have shown that a diverse assortment of cooperative genetic and epigenetic events drive the resistant phenotype. Herein, we summarize results using a variety of genomic technologies to highlight the power of this methodology in providing insight into the biological mechanisms that impart resistant disease.
尽管由于风险分层的细化和治疗的选择性强化,新诊断的小儿急性淋巴细胞白血病的治疗结果有了很大进展,但复发性白血病的预后仍显著滞后。了解导致耐药性的潜在生物学途径对于开发预防复发和治疗复发性疾病的新方法至关重要。在这个个性化医疗时代,高通量基因组技术有潜力彻底改变癌症治疗。利用这些先进技术,我们和其他人已经表明,各种各样的协同基因和表观遗传事件驱动了耐药表型。在此,我们总结使用各种基因组技术的结果,以突出这种方法在深入了解赋予耐药疾病的生物学机制方面的作用。