EA2679, Faculté de Médecine de Lille, Pôle Recherche, Lille, France.
Clin Pharmacol Ther. 2010 Dec;88(6):854-61. doi: 10.1038/clpt.2010.212. Epub 2010 Oct 27.
We investigated whether genetic polymorphisms in the promoter region of the proapoptotic β-2 adrenergic receptor gene (ADRB2) influence treatment-induced changes in ADRB2 expression in leukemia cells and response to chemotherapy. The ADRB2 promoter region was genotyped in germline DNA from 369 children with acute lymphoblastic leukemia (ALL). For 95 of the patients, sufficient RNA was available before and after in vivo treatment to assess treatment-induced gene expression changes in ALL cells. After treatment, the median ADRB2 mRNA expression was ninefold lower in leukemia cells of patients who ultimately relapsed as compared with patients who remained in continuous complete remission (CCR). Polymorphisms in the ADRB2 promoter were significantly linked to methotrexate (MTX)-induced upregulation in ADRB2 gene expression in ALL cells. Moreover, the ADRB2 promoter haplotype was significantly related to early treatment response in 245 children with ALL who received uniform treatment. We conclude that germline polymorphisms in ADRB2 are linked to the antileukemic effects of ALL chemotherapy.
我们研究了凋亡促进型β-2 肾上腺素能受体基因(ADRB2)启动子区域的遗传多态性是否影响白血病细胞中 ADRB2 表达的治疗诱导变化和对化疗的反应。对 369 例急性淋巴细胞白血病(ALL)患儿的种系 DNA 中的 ADRB2 启动子区域进行了基因分型。对于 95 名患者,在体内治疗前后有足够的 RNA 可用于评估 ALL 细胞的治疗诱导基因表达变化。治疗后,与持续完全缓解(CCR)的患者相比,最终复发的患者白血病细胞中 ADRB2 mRNA 的表达中位数低 9 倍。ADRB2 启动子的多态性与 ALL 细胞中 ADRB2 基因表达的甲氨蝶呤(MTX)诱导上调显著相关。此外,在接受统一治疗的 245 例 ALL 患儿中,ADRB2 启动子单倍型与早期治疗反应显著相关。我们的结论是,ADRB2 中的种系多态性与 ALL 化疗的抗白血病作用有关。