Expression of c-fos correlates with IFN-alpha responsiveness in Philadelphia chromosome positive chronic myelogenous leukemia.

Cytokines and molecular therapy Pub Date : 1995-03-01
B Eibl, E Greiter, K Grünewald, G Gastl, K Weyrer, J Thaler, W Aulitzky, F Herrmann, U Rapp, C Huber
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Abstract

This study evaluates (i) constitutive levels of oncogene and p53 transcripts in chronic phase CML patients and (ii) their modulations subsequent to in vivo therapy with rIFN-alpha 2c. Peripheral blood mononuclear cells (pbmc) and bone marrow cells of 26 patients were examined for c-fos, c-myc, p53 and the hybrid bcr/abl mRNA levels. Results indicated that (i) constitutive c-fos transcript levels are significantly higher in patients subsequently responding to IFN-alpha therapy (p < 0.01) and positively correlated with the proportion of lymphocytes (r = 0.6895, p < 0.01) and negatively with the proportion of immature cells (r = -0.568, p < 0.01) contained in the pbmc preparations tested, (ii) constitutive mRNA levels of the hybrid bcr/abl, c-myc and p53 are positively correlated with each other, but failed to relate to disease parameters, and (iii) acute and chronic in vivo exposure to IFN-alpha is accompanied by upregulation of c-fos and downregulation of c-myc mRNA levels in responder patients.

在费城染色体阳性的慢性粒细胞白血病中c-fos的表达与ifn - α反应性相关。
本研究评估了(1)慢性期CML患者的癌基因和p53转录本的组成水平,以及(2)在体内用rifn - α 2c治疗后它们的调节。检测26例患者外周血单个核细胞(pbmc)和骨髓细胞c-fos、c-myc、p53和bcr/abl杂交mRNA水平。结果表明:(1)ifn - α治疗后患者的c-fos组成转录物水平显著升高(p < 0.01),与淋巴细胞比例呈正相关(r = 0.6895, p < 0.01),与pbmc制剂中未成熟细胞比例呈负相关(r = -0.568, p < 0.01); (2) bcr/abl、c-myc和p53的组成mRNA水平呈正相关。但未能与疾病参数相关,并且(iii)急性和慢性体内暴露于ifn - α时,应答患者伴有c-fos的上调和c-myc mRNA水平的下调。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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