Department of Veterinary Internal Medicine, Graduate School of Agricultural and Life Sciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-8657, Japan
Anticancer Res. 2013 Dec;33(12):5317-23.
One of the major causes of failure in chemotherapy for patients with acute lymphoblastic leukemia (ALL) is the acquisition of multidrug resistance (MDR). Predominant mechanisms for MDR acquisition include the overexpression of efflux pumps. In the present study, the regulation of the expression of two genes that encode efflux pumps, ATP-binding cassette, sub-family B, member 1 (ABCB1) and ABCG2, through mitogen-activated protein kinase (MAPK) pathways was examined.
ABCB1 and ABCG2 mRNAs were quantified in a T-ALL cell line, CCRF-HSB-2 and a B-ALL cell line, YAMN90 using real-time RT-PCR. Changes in the mRNA amounts of these genes were examined after activation or inhibition of MAPK/extracellular signal-regulated kinase (ERK) pathway and c-Jun NH2-terminal kinase (JNK) pathway.
Activation of MAPK/ERK pathway up-regulated ABCB1 expression but down-regulated ABCG2 expression. Activation of JNK pathway up-regulated ABCG2 gene expression.
The expressions of ABCB1 and ABCG2 genes were regulated through MAPK/ERK and JNK pathways in the human ALL cell lines.
急性淋巴细胞白血病(ALL)患者化疗失败的主要原因之一是获得多药耐药(MDR)。获得 MDR 的主要机制包括外排泵的过度表达。在本研究中,通过丝裂原活化蛋白激酶(MAPK)通路研究了编码两种外排泵的基因 ABCB1 和 ABCG2 的表达调控。
使用实时 RT-PCR 定量测定 T-ALL 细胞系 CCRF-HSB-2 和 B-ALL 细胞系 YAMN90 中的 ABCB1 和 ABCG2 mRNA。在激活或抑制 MAPK/细胞外信号调节激酶(ERK)通路和 c-Jun NH2-末端激酶(JNK)通路后,检查这些基因的 mRNA 量的变化。
MAPK/ERK 通路的激活上调了 ABCB1 的表达,但下调了 ABCG2 的表达。JNK 通路的激活上调了 ABCG2 基因的表达。
在人 ALL 细胞系中,ABCB1 和 ABCG2 基因的表达通过 MAPK/ERK 和 JNK 通路进行调节。