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Inhibition of abl Oncogene Tyrosine Kinase Induces Erythroid Differentiation of Human Myelogenous Leukemia K562 Cells

机译:抑制abl癌基因酪氨酸激酶诱导人骨髓性白血病K562细胞的类红细胞分化

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摘要

The human chronic myelogenous leukemia cell line K562 expresses a structurally altered c‐abl protein with tyrosine kinase activity. Erythroid differentiation of K562 cells was induced by tyrosine kinase inhibitors, but not by other kinase inhibitors. Treatment of K562 cells with 5'd(TACTGGCCGCTG‐AAGGGC)3′, complementary to the second exon (codons 2 to 7) of c‐abl mRNA, inhibited cell growth and induced benzidine‐positive cells in a dose‐dependent manner. However, exposure to the sense oligomer did not induce erythroid differentiation of the cells. These results suggest that inhibition of abl tyrosine kinase activity is closely related to induction of erythroid differentiation of K562 cells. A multidrug‐resistant subline (K562R) was induced to undergo erythroid differentiation by tyrosine kinase inhibitors such as genistein or herbimycin A as effectively as the parent K562 cells were. Therefore, tyrosine kinase inhibitors might be useful as cancer chemotherapeutic agents against some multidrug‐resistant leukemias having abnormally high activity of oncogene tyrosine kinase(s).
机译:人类慢性粒细胞白血病细胞株K562表达具有酪氨酸激酶活性的结构改变的c-abl蛋白。酪氨酸激酶抑制剂可诱导K562细胞的类红细胞分化,但其他激酶抑制剂则不会。用5'd(TACTGGCCGCTG-AAGGGC)3'与c-abl mRNA的第二个外显子(第2至7个密码子)互补来治疗K562细胞,以剂量依赖的方式抑制细胞生长并诱导联苯胺阳性细胞。但是,暴露于有义寡聚物不会诱导细胞的类红细胞分化。这些结果表明,抑制abl酪氨酸激酶活性与诱导K562细胞的类红细胞分化密切相关。酪氨酸激酶抑制剂(如染料木黄酮或除草素A)可诱导多药耐药亚系(K562R)分化为类红细胞,与亲本K562细胞一样有效。因此,酪氨酸激酶抑制剂可作为抗癌药物,用于治疗某些癌基因酪氨酸激酶活性异常高的多药耐药性白血病。

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