Takenokuchi M, Saigo K, Nakamachi Y, Kawano S, Hashimoto M, Fujioka T, Koizumi T, Tatsumi E, Kumagai S
Department of Clinical Laboratory, Kobe University Hospital, Kobe, Japan.
Acta Haematol. 2006;116(1):30-40. doi: 10.1159/000092345.
Peroxisome proliferator-activated receptor-gamma (PPARgamma), a member of the nuclear receptor superfamily, has been detected in several human leukemia cells. Recent studies reported that PPARgamma ligands inhibit cell proliferation and induce apoptosis in both normal and malignant B-lineage cells. We investigated the expression of PPARgamma and the effects of PPARgamma ligands on UTree-O2, Bay91 and 380, three B-cell acute lymphoblastic leukemia (B-ALL) cell lines with t(14;18), which show a poor prognosis, accompanying c-myc abnormality. Western blot analysis identified expression of PPARgamma protein and real-time PCR that of PPARgamma mRNA on the three cell lines. Troglitazone (TGZ), a synthetic PPARgamma ligand, inhibited cell growth in these cell lines in a dose-dependent manner, which was associated with G(1) cell cycle arrest and apoptosis. We also found this effect PPARgamma independent since PPARgamma antagonists failed to reverse this effect. We assessed the expression of c-myc, an apoptosis-regulatory gene, since c-myc abnormality was detected in most B-ALL cells with t(14;18). TGZ was found to dose-dependently downregulate the expression of c-myc mRNA and c-myc protein in the three cell lines. These results suggest that TGZ inhibits cell growth via induction of G(1) cell cycle arrest and apoptosis in these cell lines and that TGZ-induced apoptosis, at least in part, may be related to the downregulation of c-myc expression. Moreover, the downregulation of c-myc expression by TGZ may depend on a PPARgamma-independent mechanism. Further studies indicate that PPARgamma ligands may serve as a therapeutic agent in B-ALL with t(14;18).
过氧化物酶体增殖物激活受体γ(PPARγ)是核受体超家族的成员之一,已在多种人类白血病细胞中被检测到。最近的研究报道,PPARγ配体可抑制正常和恶性B淋巴细胞系细胞的增殖并诱导其凋亡。我们研究了PPARγ在伴有c-myc异常且预后较差的三种t(14;18) B细胞急性淋巴细胞白血病(B-ALL)细胞系UTree-O2、Bay91和380中的表达情况,以及PPARγ配体对它们的影响。蛋白质免疫印迹分析确定了这三种细胞系中PPARγ蛋白的表达,实时定量PCR确定了PPARγ mRNA的表达。合成的PPARγ配体曲格列酮(TGZ)以剂量依赖的方式抑制这些细胞系的生长,这与G(1)期细胞周期停滞和凋亡有关。我们还发现这种效应不依赖于PPARγ,因为PPARγ拮抗剂无法逆转这种效应。由于在大多数t(14;18)的B-ALL细胞中检测到c-myc异常,我们评估了凋亡调节基因c-myc的表达。结果发现,TGZ可使这三种细胞系中c-myc mRNA和c-myc蛋白的表达呈剂量依赖性下调。这些结果表明,TGZ通过诱导这些细胞系G(1)期细胞周期停滞和凋亡来抑制细胞生长,并且TGZ诱导的凋亡至少部分可能与c-myc表达下调有关。此外,TGZ对c-myc表达的下调可能依赖于一种不依赖PPARγ的机制。进一步的研究表明,PPARγ配体可能作为治疗t(14;18) B-ALL的一种治疗药物。