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The expression of cellular retinoid binding proteins in non-APL leukemic cells and its association with retinoid sensitivity.

机译:细胞类视黄醇结合蛋白在非APL白血病细胞中的表达及其与类视黄醇敏感性的关系。

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摘要

Retinoic acid (RA) has important effects on cell differentiation and cell growth and on normal embryonic development. Intracellular retinoid signaling induced by endogenous or exogenous RA is regulated by retinoid binding proteins such as CRBPI, CRABPI and CRABPII and there are data suggesting that the expression of these proteins can influence the sensitivity to the growth inhibitory effects of ATRA. In this study, we investigated the basal and ATRA-induced expression of CRBPI and CRABPI and II in leukemic cell lines and in cells from patients with acute myeloid leukemia (AML). CRBPI as well as CRABPI and II were expressed in all tested cell lines and in leukemic cells from all 18 AML-patients. CRABPII mRNA expression was more abundant than CRBPI and CRABPI in both the cell lines and the patient cells but the levels compared the house keeping gene was lower in the patient cells. In all cell lines and in 69% of the patient samples, ATRA did upregulate CRABPII whereas CRBPI exhibited a varying response and CRABPI was more commonly downregulated. The sensitivity to the growth inhibitory effects of ATRA did not correlate with the basal expression of any of these proteins. However, ATRA-induced upregulation of CRABPII did significantly correlate with the ATRA sensitivity (p < 0.005) as well as with ATRA-induced upregulation of the retinoid receptor RARbeta (p < 0.05). We conclude that the retinoid binding proteins CRBPI and CRABPI and II are expressed in myeloid leukemic cells of non-M3 type but that the level of expression does not affect ATRA sensitivity.
机译:维甲酸(RA)对细胞分化和细胞生长以及正常胚胎发育有重要影响。内源性或外源性RA诱导的细胞内类维生素A信号传导受类维生素A结合蛋白(例如CRBPI,CRABPI和CRABPII)调控,并且有数据表明这些蛋白的表达可以影响对ATRA的生长抑制作用的敏感性。在这项研究中,我们调查了白血病细胞系和急性髓细胞性白血病(AML)患者细胞中基础和ATRA诱导的CRBPI和CRABPI和II的表达。 CRBPI以及CRABPI和II在所有测试的细胞系和所有18位AML患者的白血病细胞中表达。在细胞系和患者细胞中,CRABPII mRNA的表达均比CRBPI和CRABPI丰富,但是与之相比,持家基因的水平在患者细胞中较低。在所有细胞系和69%的患者样品中,ATRA确实上调了CRABPII,而CRBPI则显示出变化的应答,而CRABPI更常见地被下调。对ATRA的生长抑制作用的敏感性与任何这些蛋白的基础表达均不相关。然而,ATRA诱导的CRABPII上调与ATRA敏感性(p <0.005)以及ATRA诱导的类维生素A受体RARbeta的上调(p <0.05)显着相关。我们得出结论,类视黄醇结合蛋白CRBPI和CRABPI和II在非M3型髓样白血病细胞中表达,但表达水平不影响ATRA敏感性。

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