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c-myc和c-myb的抑制与IL6或LIF诱导的终末分化紧密相关,而非与髓系白血病细胞的生长抑制相关。

Suppression of c-myc and c-myb is tightly linked to terminal differentiation induced by IL6 or LIF and not growth inhibition in myeloid leukemia cells.

作者信息

Hoffman-Liebermann B, Liebermann D A

机构信息

Department of Biochemistry and Biophysics, University of Pennsylvania School of Medicine, Philadelphia 19104.

出版信息

Oncogene. 1991 Jun;6(6):903-9.

PMID:1906157
Abstract

Cell proliferation and differentiation are intimately related processes where the proto-oncogenes c-myc and c-myb have been implicated to play a role. Previously, we have shown that both c-myc and c-myb were induced in normal myeloid precursors when the cells were stimulated for growth, were expressed in the autonomously proliferating myeloid leukemic M1 cell line and were rapidly suppressed in both normal and M1 cells following induction of terminal differentiation associated with growth arrest. In order to distinguish molecular events associated with terminal differentiation versus those due to growth inhibition, as well as to increase our understanding of the role of the proto-oncogenes c-myc and c-myb in both of these cellular processes, in this work we have studied the expression of c-myc and c-myb in M1 cells induced for growth inhibition associated with terminal differentiation (via treatment with the physiological inducers IL6 or leukemia inhibitory factor mean value of LIF), partial differentiation (using IL1 or LPS) or no detectable differentiation properties (using IFN beta or IFN gamma). We show that, for all the treatments used in this study, down regulation of the proto-oncogenes c-myc and c-myb occurred only when M1 cells were stimulated to undergo terminal differentiation. In addition, we transfected the M1 cell line with a vector containing the c-myc gene under control of the beta-actin promoter, so that c-myc was no longer down regulated by IL6 or LIF. Previously, we have shown that in the presence of the myeloid differentiation inducers IL6 or LIF, these M1myc cells were blocked at an intermediate stage of myeloid differentiation and continued to proliferate. In sharp contrast to their altered response to IL6 or LIF, M1myc cells were as responsive as the parental M1 cells to growth suppression by the different antiproliferative compounds which do not induce terminal differentiation. Thus, continued expression of c-myc had no effect on growth suppression induced by IL1, IFN beta, IFN gamma and LPS. Taken together, these results indicate that c-myc and c-myb down regulation is not necessary for growth suppression, but down regulation of c-myc is, and c-myb may be, essential for terminal differentiation.

摘要

细胞增殖和分化是密切相关的过程,原癌基因c-myc和c-myb被认为在其中发挥作用。此前,我们已经表明,当正常髓系前体细胞受到生长刺激时,c-myc和c-myb都会被诱导表达,它们在自主增殖的髓系白血病M1细胞系中表达,并且在与生长停滞相关的终末分化诱导后,在正常细胞和M1细胞中都会迅速被抑制。为了区分与终末分化相关的分子事件和那些由于生长抑制引起的分子事件,以及增进我们对原癌基因c-myc和c-myb在这两个细胞过程中作用的理解,在这项工作中,我们研究了c-myc和c-myb在因与终末分化相关的生长抑制(通过用生理诱导剂IL6或白血病抑制因子LIF处理)、部分分化(使用IL1或LPS)或无明显分化特性(使用IFNβ或IFNγ)而被诱导的M1细胞中的表达。我们表明,对于本研究中使用的所有处理,只有当M1细胞被刺激进行终末分化时,原癌基因c-myc和c-myb才会下调。此外,我们用一个含有在β-肌动蛋白启动子控制下的c-myc基因的载体转染M1细胞系,使得c-myc不再被IL6或LIF下调。此前,我们已经表明,在存在髓系分化诱导剂IL6或LIF的情况下,这些M1myc细胞在髓系分化的中间阶段被阻断并继续增殖。与它们对IL6或LIF的改变的反应形成鲜明对比的是,M1myc细胞对不同的不诱导终末分化的抗增殖化合物的生长抑制反应与亲代M1细胞一样。因此,c-myc的持续表达对IL1、IFNβ、IFNγ和LPS诱导的生长抑制没有影响。综上所述,这些结果表明,c-myc和c-myb的下调对于生长抑制不是必需的,但c-myc的下调是终末分化所必需的,而c-myb可能也是必需的。

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