Tyr352 as a Predominant Phosphosite in the Understudied Kinase and Molecular Target, HIPK1: Implications for Cancer Therapy.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
ACS Applied Bio Materials Pub Date : 2024-03-01 Epub Date: 2024-03-18 DOI:10.1089/omi.2023.0244
Diya Sanjeev, Mejo George, Levin John, Athira Perunelly Gopalakrishnan, Pahal Priyanka, Spoorthi Mendon, Tanuja Yandigeri, Mahammad Nisar, Muhammad Nisar, Saptami Kanekar, Rex Devasahayam Arokia Balaya, Rajesh Raju
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引用次数: 0

Abstract

Homeodomain-interacting protein kinase 1 (HIPK1) is majorly found in the nucleoplasm. HIPK1 is associated with cell proliferation, tumor necrosis factor-mediated cellular apoptosis, transcription regulation, and DNA damage response, and thought to play significant roles in health and common diseases such as cancer. Despite this, HIPK1 remains an understudied molecular target. In the present study, based on a systematic screening and mapping approach, we assembled 424 qualitative and 44 quantitative phosphoproteome datasets with 15 phosphosites in HIPK1 reported across multiple studies. These HIPK1 phosphosites were not currently attributed to any functions. Among them, Tyr352 within the kinase domain was identified as the predominant phosphosite modulated in 22 differential datasets. To analyze the functional association of HIPK1 Tyr352, we first employed a stringent criterion to derive its positively and negatively correlated protein phosphosites. Subsequently, we categorized the correlated phosphosites in known interactors, known/predicted kinases, and substrates of HIPK1, for their prioritized validation. Bioinformatics analysis identified their significant association with biological processes such as the regulation of RNA splicing, DNA-templated transcription, and cellular metabolic processes. HIPK1 Tyr352 was also identified to be upregulated in Her2+ cell lines and a subset of pancreatic and cholangiocarcinoma tissues. These data and the systems biology approach undertaken in the present study serve as a platform to explore the functional role of other phosphosites in HIPK1, and by extension, inform cancer drug discovery and oncotherapy innovation. In all, this study highlights the comprehensive phosphosite map of HIPK1 kinase and the first of its kind phosphosite-centric analysis of HIPK1 kinase based on global-level phosphoproteomics datasets derived from human cellular differential experiments across distinct experimental conditions.

Tyr352 作为未充分研究的激酶和分子靶标 HIPK1 的主要磷酸化位点:对癌症治疗的意义
Homeodomain-interacting protein kinase 1(HIPK1)主要存在于核质中。HIPK1 与细胞增殖、肿瘤坏死因子介导的细胞凋亡、转录调控和 DNA 损伤反应有关,被认为在健康和癌症等常见疾病中发挥着重要作用。尽管如此,HIPK1 仍是一个未被充分研究的分子靶点。在本研究中,我们基于系统筛选和制图方法,收集了424个定性和44个定量磷酸化蛋白质组数据集,其中有15个磷酸位点在HIPK1中被多个研究报道。这些 HIPK1 磷酸化位点目前没有任何功能。其中,激酶结构域内的 Tyr352 被确定为 22 个差异数据集中主要的被调控磷酸化位点。为了分析 HIPK1 Tyr352 的功能关联,我们首先采用了一个严格的标准来得出其正相关和负相关的蛋白质磷酸化位点。随后,我们对已知相互作用者、已知/预测激酶和 HIPK1 底物中的相关磷酸位点进行了分类,以便对其进行优先验证。生物信息学分析确定了这些磷酸位点与 RNA 剪接调控、DNA 促转录和细胞代谢过程等生物过程的重要关联。还发现 HIPK1 Tyr352 在 Her2+ 细胞系以及胰腺癌和胆管癌组织亚群中上调。这些数据和本研究中采用的系统生物学方法为探索 HIPK1 中其他磷酸位点的功能作用提供了一个平台,进而为癌症药物发现和肿瘤治疗创新提供了信息。总之,本研究展示了 HIPK1 激酶的全面磷酸化位点图,并首次基于不同实验条件下人体细胞差异实验所获得的全局水平磷酸化蛋白质组学数据集,对 HIPK1 激酶进行了以磷酸化位点为中心的分析。
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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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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