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生长分化因子 3 诱导癌症干细胞模型中与分化相关基因的表达,并保护它们免受维甲酸诱导的细胞凋亡。

Growth and differentiation factor 3 induces expression of genes related to differentiation in a model of cancer stem cells and protects them from retinoic acid-induced apoptosis.

机构信息

Institute of Medical Biotechnology, Department of Biotechnology, Technische Universität Berlin, Berlin, Germany.

出版信息

PLoS One. 2013 Aug 12;8(8):e70612. doi: 10.1371/journal.pone.0070612. eCollection 2013.

Abstract

Misexpression of growth factors, particularly those related to stem cell-like phenotype, is often observed in several cancer types. It has been found to influence parameters of disease progression like cell proliferation, differentiation, maintenance of undifferentiated phenotype and modulation of the immune system. GDF3 is a TGFB family member associated with pluripotency and differentiation during embryonic development that has been previously reported to be re-expressed in a number of cancer types. However, its role in tumor development and progression has not been clarified yet. In this study we decipher the role of GDF3 in an in vitro model of cancer stem cells, NCCIT cells. By classical approach to study protein function combined with high-throughput technique for transcriptome analysis and differentiation assays we evaluated GDF3 as a potential therapeutic target. We observed that GDF3 robustly induces a panel of genes related to differentiation, including several potent tumor suppressors, without impacting the proliferative capacity. Moreover, we report for the first time the protective effect of GDF3 against retinoic acid-induced apoptosis in cells with stem cell-like properties. Our study implies that blocking of GDF3 combined with retinoic acid-treatment of solid cancers is a compelling direction for further investigations, which can lead to re-design of cancer differentiation therapies.

摘要

生长因子的异常表达,特别是那些与干细胞样表型相关的生长因子,在几种癌症类型中经常观察到。它被发现影响疾病进展的参数,如细胞增殖、分化、未分化表型的维持和免疫系统的调节。GDF3 是 TGFB 家族的一员,与胚胎发育过程中的多能性和分化有关,先前有报道称它在多种癌症类型中重新表达。然而,它在肿瘤发展和进展中的作用尚未阐明。在这项研究中,我们在 NCCIT 细胞这一癌症干细胞体外模型中解析了 GDF3 的作用。通过研究蛋白质功能的经典方法结合高通量技术进行转录组分析和分化实验,我们评估了 GDF3 作为一种潜在的治疗靶点的可能性。我们观察到,GDF3 强烈诱导一组与分化相关的基因,包括几种有效的肿瘤抑制因子,而不影响增殖能力。此外,我们首次报道了 GDF3 对具有干细胞样特性的细胞中维甲酸诱导的细胞凋亡的保护作用。我们的研究表明,阻断 GDF3 与维甲酸联合治疗实体瘤是进一步研究的一个有吸引力的方向,这可能导致癌症分化治疗的重新设计。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80e5/3741270/7bbafd20c3fe/pone.0070612.g001.jpg

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