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pp32 降低诱导 TSU-Pr1 细胞分化。

pp32 reduction induces differentiation of TSU-Pr1 cells.

作者信息

Brody Jonathan R, Kadkol Shrihari S, Hauer M Claire, Rajaii Fatemeh, Lee Jessica, Pasternack Gary R

机构信息

Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21231, USA.

出版信息

Am J Pathol. 2004 Jan;164(1):273-83. doi: 10.1016/S0002-9440(10)63117-3.

DOI:10.1016/S0002-9440(10)63117-3
PMID:14695340
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1602226/
Abstract

pp32 (ANP32A) is a nuclear phosphoprotein expressed as a nonmutated form in self-renewing cell populations and neoplastic cells. Mechanistically, pp32 may regulate pathways important in the process of differentiation as part of separate complexes inhibiting histone acetylation and regulating immediate-early and cytokine mRNA stability. Prostatic adenocarcinomas express pp32 in a differentiation related manner-well-differentiated tumors express lower levels of pp32 than poorly differentiated tumors. In benign prostate, pp32 is expressed in basal cells but not in terminally differentiated glandular cells. Based on these observations, we hypothesized that reduction of pp32 expression might be an important differentiation signal. We used anti-sense pp32 and RNAi transfection to study the effects of reduced pp32 expression in the TSU-Pr1 carcinoma cell line. pp32 reduction induced TSU-Pr1 cells to differentiate into neuronal-like cells with associated inhibition of growth. Reduction of pp32 and consequent differentiation were accompanied by a marked reduction in expression of SET, which complexes with pp32, by a marked change in acetylation status of histone H4, and by further differential expression of genes in differentiation pathways. Thus, reduction of pp32 in the undifferentiated TSU-Pr1 neoplastic cell line induces differentiation and thus may be an element of a differentiation control pathway in both normal and neoplastic cells.

摘要

pp32(ANP32A)是一种核磷蛋白,在自我更新细胞群体和肿瘤细胞中以非突变形式表达。从机制上讲,pp32可能作为抑制组蛋白乙酰化以及调节即刻早期基因和细胞因子mRNA稳定性的独立复合物的一部分,调节分化过程中重要的信号通路。前列腺腺癌以与分化相关的方式表达pp32——高分化肿瘤表达的pp32水平低于低分化肿瘤。在良性前列腺组织中,pp32在基底细胞中表达,但在终末分化的腺细胞中不表达。基于这些观察结果,我们推测pp32表达的降低可能是一个重要的分化信号。我们使用反义pp32和RNAi转染来研究降低pp32表达对TSU-Pr1癌细胞系的影响。pp32表达降低诱导TSU-Pr1细胞分化为神经元样细胞,并伴有生长抑制。pp32表达降低及随之而来的分化伴随着与pp32结合的SET表达显著降低、组蛋白H4乙酰化状态的明显改变以及分化信号通路中基因的进一步差异表达。因此,未分化的TSU-Pr1肿瘤细胞系中pp32表达的降低诱导了分化,因此可能是正常细胞和肿瘤细胞中分化控制信号通路的一个组成部分。

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本文引用的文献

1
Neuroendocrine expression in node positive prostate cancer: correlation with systemic progression and patient survival.淋巴结阳性前列腺癌中的神经内分泌表达:与全身进展和患者生存的相关性。
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Analysis of the adenovirus E1B-55K-anchored proteome reveals its link to ubiquitination machinery.腺病毒E1B - 55K锚定蛋白质组分析揭示其与泛素化机制的联系。
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3
The oncoprotein Set/TAF-1beta, an inhibitor of histone acetyltransferase, inhibits active demethylation of DNA, integrating DNA methylation and transcriptional silencing.癌蛋白Set/TAF-1β是组蛋白乙酰转移酶的抑制剂,可抑制DNA的主动去甲基化,从而整合DNA甲基化与转录沉默。
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Histone deacetylases and cancer: causes and therapies.组蛋白去乙酰化酶与癌症:病因与疗法
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5
Regulation of histone acetylation and transcription by nuclear protein pp32, a subunit of the INHAT complex.核蛋白pp32(INHAT复合物的一个亚基)对组蛋白乙酰化和转录的调控
J Biol Chem. 2002 Apr 19;277(16):14005-10. doi: 10.1074/jbc.M112455200. Epub 2002 Feb 5.
6
Neuroendocrine differentiation in human prostate cancer. Morphogenesis, proliferation and androgen receptor status.人类前列腺癌中的神经内分泌分化。形态发生、增殖与雄激素受体状态。
Ann Oncol. 2001;12 Suppl 2:S141-4. doi: 10.1093/annonc/12.suppl_2.s141.
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The histone deacetylase inhibitor suberoylanilide hydroxamic acid induces differentiation of human breast cancer cells.组蛋白去乙酰化酶抑制剂辛二酰苯胺异羟肟酸可诱导人乳腺癌细胞分化。
Cancer Res. 2001 Dec 1;61(23):8492-7.
8
Interleukin-6- and cyclic AMP-mediated signaling potentiates neuroendocrine differentiation of LNCaP prostate tumor cells.白细胞介素-6和环磷酸腺苷介导的信号传导增强LNCaP前列腺肿瘤细胞的神经内分泌分化。
Mol Cell Biol. 2001 Dec;21(24):8471-82. doi: 10.1128/MCB.21.24.8471-8482.2001.
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Histone deacetylase inhibitors induce remission in transgenic models of therapy-resistant acute promyelocytic leukemia.组蛋白去乙酰化酶抑制剂可诱导治疗耐药性急性早幼粒细胞白血病转基因模型缓解。
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TSU-Pr1 and JCA-1 cells are derivatives of T24 bladder carcinoma cells and are not of prostatic origin.TSU-Pr1细胞和JCA-1细胞是T24膀胱癌细胞的衍生物,并非来源于前列腺。
Cancer Res. 2001 Sep 1;61(17):6340-4.