慢性淋巴细胞白血病
癌症研究
氟达拉滨
贾纳斯激酶
JAK-STAT信号通路
STAT1
细胞凋亡
斯达
医学
白血病
STAT蛋白
车站3
酪氨酸激酶
信号转导
免疫学
生物
内科学
受体
干扰素
细胞生物学
化疗
环磷酰胺
生物化学
作者
Luis Martínez‐Lostao,Javier Briones,Ignasi Forné,Mónica Martínez‐Gallo,Beatriz Ferrer,Jordi Sierra,J. L. Rodríguez-Sánchez,C. Juárez
标识
DOI:10.1080/10428190400018398
摘要
AbstractSignal transducers and activators of transcription (STAT) proteins comprise a family of transcription factors that have been implicated in tumoral transformation, especially in hematological malignancies. Because of this, the JAK/STAT pathway is attractive as a therapeutic target in these tumors. In the present study, we analyzed the ability of fludarabine and two JAK kinase inhibitors, AG490 and WHI-P131, to block STAT1 activation and induce apoptosis on B-cell chronic lymphocytic leukemia (B-CLL) cells. All drugs were able to induce a high percentage of apoptosis on B-CLL cells from all patients studied. However, only AG490 and WHI-P131 were able to strongly suppress the STAT1 activation of B-CLL cells. In conclusion, our data show that JAK kinase inhibitors, such as AG490 and WHI-P131 are able to inhibit the STAT1 pathway on B-CLL cells and are strong inductors of apoptosis on these cells.KeywordsSTAT1B-CLLapoptosisfludarabineAG490WHI-P131
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