Molecular Oncology Research Institute and Division of Hematology/Oncology, Tufts Medical Center, 800 Washington Street, Box 5609, Boston, MA 02111, USA.
Curr Hematol Malig Rep. 2013 Mar;8(1):71-80. doi: 10.1007/s11899-012-0150-1.
The chronic leukemias, including chronic myeloid leukemia (CML), the Philadelphia-negative myeloproliferative neoplasms (MPNs), and chronic lymphocytic leukemia (CLL), have been characterized extensively for abnormalities of cellular signaling pathways. This effort has led to the elucidation of the central role of dysregulated tyrosine kinase signaling in the chronic myeloid neoplasms and of constitutive B-cell receptor signaling in CLL. This, in turn, has stimulated the development of small molecule inhibitors of these signaling pathways for therapy of chronic leukemia. Although the field is still in its infancy, the clinical results with these agents have ranged from encouraging (CLL) to spectacular (CML). In this review, we summarize recent studies that have helped to define the signaling pathways critical to the pathogenesis of the chronic leukemias. We also discuss correlative studies emerging from clinical trials of drugs targeting these pathways.
慢性白血病,包括慢性髓性白血病(CML)、费城阴性骨髓增殖性肿瘤(MPN)和慢性淋巴细胞白血病(CLL),其细胞信号通路异常已得到广泛研究。这一努力揭示了酪氨酸激酶信号的失调在慢性髓性白血病中的核心作用,以及 B 细胞受体信号在 CLL 中的组成性作用。这反过来又刺激了这些信号通路的小分子抑制剂的开发,用于治疗慢性白血病。尽管该领域仍处于起步阶段,但这些药物的临床结果从令人鼓舞(CLL)到惊人(CML)不等。在这篇综述中,我们总结了最近的研究,这些研究有助于确定对慢性白血病发病机制至关重要的信号通路。我们还讨论了这些通路药物临床试验中出现的相关研究。