了解 Pax5 在多西他赛耐药神经内分泌样前列腺癌发展过程中的功能。

IF 8.1 1区 生物学 Q1 CELL BIOLOGY
Sreyashi Bhattacharya, Hannah L Harris, Ridwan Islam, Sanika Bodas, Navatha Polavaram, Juhi Mishra, Dipanwita Das, Parthasarathy Seshacharyulu, Achyuth Kalluchi, Anirban Pal, Manish Kohli, Subodh M Lele, Michael Muders, Surinder K Batra, Paramita M Ghosh, Kaustubh Datta, M Jordan Rowley, Samikshan Dutta
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引用次数: 0

摘要

当前雄激素受体信号抑制剂(ARSI)疗法的抗药性导致治疗诱导的神经内分泌样前列腺癌(t-NEPC)发病率上升。这种高度侵袭性的亚型主要具有小细胞样特征,对紫杉类化疗具有耐药性,总生存期很短。t-NEPC 大多采用铂类药物与依托泊苷或紫杉类药物联合治疗,选择性较差,全身毒性大,这往往限制了其临床潜力。在t-NEPC转化过程中,腺癌会失去腔内特征,并具有神经基质特征。t-NEPC的适应性神经元特征是否是造成这种紫杉类药物耐药性的原因,目前仍是未知数。来自患者基因表达数据库的通路分析表明,t-NEPC 会上调与增强细胞网络相关的各种神经元通路。为了找出可能对促进t-NEPC中神经元特征基因表达起重要作用的转录因子(TF),我们在NE样细胞系模型中进行了ATAC-Seq、乙酰化组蛋白ChIP-seq和RNA-seq,并分析了转录活跃和显著富集的神经内分泌样(NE样)癌症特异性基因的启动子。我们的研究结果表明,Pax5 可能是神经元基因表达的一个重要转录因子,并且对 t-NEPC 具有特异性。通路分析表明,Pax5的表达参与了轴突导向、神经递质调节和神经元粘附,而这些对于强大的细胞通讯至关重要。进一步的研究结果表明,消耗 Pax5 会破坏 NE 样细胞中神经元介导的细胞通讯,降低表面生长因子受体的激活,从而使它们对多西他赛疗法敏感。此外,Pax5 启动子 CpG 岛的 t-NEPC 特异性羟甲基化有利于 Pbx1 的结合,从而诱导 Pax5 的表达。根据我们的研究,我们得出结论:持续暴露于ARSI疗法会导致t-NEPC中的表观遗传学修饰和Pax5激活,从而促进采用抗紫杉类药物的NE样癌所需基因的表达。因此,以Pax5轴为靶点可有利于恢复其对紫杉类药物的敏感性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Understanding the function of Pax5 in development of docetaxel-resistant neuroendocrine-like prostate cancers.

Understanding the function of Pax5 in development of docetaxel-resistant neuroendocrine-like prostate cancers.

Resistance to the current Androgen Receptor Signaling Inhibitor (ARSI) therapies has led to higher incidences of therapy-induced neuroendocrine-like prostate cancer (t-NEPC). This highly aggressive subtype with predominant small-cell-like characteristics is resistant to taxane chemotherapies and has a dismal overall survival. t-NEPCs are mostly treated with platinum-based drugs with a combination of etoposide or taxane and have less selectivity and high systemic toxicity, which often limit their clinical potential. During t-NEPC transformation, adenocarcinomas lose their luminal features and adopt neuro-basal characteristics. Whether the adaptive neuronal characteristics of t-NEPC are responsible for such taxane resistance remains unknown. Pathway analysis from patient gene-expression databases indicates that t-NEPC upregulates various neuronal pathways associated with enhanced cellular networks. To identify transcription factor(s) (TF) that could be important for promoting the gene expression for neuronal characters in t-NEPC, we performed ATAC-Seq, acetylated-histone ChIP-seq, and RNA-seq in our NE-like cell line models and analyzed the promoters of transcriptionally active and significantly enriched neuroendocrine-like (NE-like) cancer-specific genes. Our results indicate that Pax5 could be an important transcription factor for neuronal gene expression and specific to t-NEPC. Pathway analysis revealed that Pax5 expression is involved in axonal guidance, neurotransmitter regulation, and neuronal adhesion, which are critical for strong cellular communications. Further results suggest that depletion of Pax5 disrupts neurite-mediated cellular communication in NE-like cells and reduces surface growth factor receptor activation, thereby, sensitizing them to docetaxel therapies. Moreover, t-NEPC-specific hydroxymethylation of Pax5 promoter CpG islands favors Pbx1 binding to induce Pax5 expression. Based on our study, we concluded that continuous exposure to ARSI therapies leads to epigenetic modifications and Pax5 activation in t-NEPC, which promotes the expression of genes necessary to adopt taxane-resistant NE-like cancer. Thus, targeting the Pax5 axis can be beneficial for reverting their taxane sensitivity.

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来源期刊
Cell Death & Disease
Cell Death & Disease CELL BIOLOGY-
CiteScore
15.10
自引率
2.20%
发文量
935
审稿时长
2 months
期刊介绍: Brought to readers by the editorial team of Cell Death & Differentiation, Cell Death & Disease is an online peer-reviewed journal specializing in translational cell death research. It covers a wide range of topics in experimental and internal medicine, including cancer, immunity, neuroscience, and now cancer metabolism. Cell Death & Disease seeks to encompass the breadth of translational implications of cell death, and topics of particular concentration will include, but are not limited to, the following: Experimental medicine Cancer Immunity Internal medicine Neuroscience Cancer metabolism
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