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ZMIZ1 乳酸化通过增加 Nanog 的转录活性影响细胞干性和胆固醇摄取,从而诱导乳腺癌对他莫昔芬耐药。

ZMIZ1 lactylation induces tamoxifen resistance in breast cancer through increasing transcriptional activity of Nanog to impact cell stemness and cholesterol uptake.

作者信息

Liu Yue, Chen Jingyu, Ma Li, Zhao Shu, Hui Xue, Xiong Wenjing, Cheng Shaoqiang, Zhang Yue

机构信息

Breast cancer Diagnosis and Treatment Center, Harbin Medical University Cancer Hospital, Harbin, China.

Department of Oncology, The Fourth Affiliated Hospital of Harbin Medical University, Harbin, China.

出版信息

Cell Biol Toxicol. 2025 Jul 16;41(1):117. doi: 10.1007/s10565-025-10068-w.

Abstract

Tamoxifen is a critical drug for the treatment of oestrogen receptor (ER)-positive breast cancer (BC), which represents the majority of BC subtypes. However, many BC tumours that initially respond eventually develop acquired Tamoxifen resistance. Bioinformatics analysis was conducted on genes affected by Tamoxifen and upregulated in Tamoxifen-resistant cells to identify the biological processes associated with Tamoxifen resistance. Metabolomics analysis was conducted to identify the metabolites that were altered in BC with tamoxifen resistance. Resistance to Tamoxifen was evaluated by cell viability, proliferation, invasion, and colony formation in vitro, and by tumour growth in vivo. Metabolomic profiling and the detection of relevant enzymes and metabolites corroborated the metabolic reprogramming towards glycolysis in tamoxifen - resistant BC. The produced lactic acid induced the lactylation of ZMIZ1. This post-translational modification at K843 (but not K537) increased protein stability by suppressing SUMOylation and ubiquitination. The elevated total level of ZMIZ1 increased the enrichment of ZMIZ1 binding to Nanog, resulting in increased transcriptional activity of Nanog, including in OCT4 and NPC2 genes. Therefore, it leads to increased stemness and cholesterol accumulation in Tamoxifen-resistant BC. Knockdown of ZMIZ1 impaired Tamoxifen resistance, but this effect was reversed by Nanog overexpression. In summary, this study identified an important mechanism underlying Tamoxifen resistance and revealed a potential association of glucose glycolysis with cholesterol metabolism through the ZMIZ1/Nanog/NPC2 axis.

摘要

他莫昔芬是治疗雌激素受体(ER)阳性乳腺癌(BC)的关键药物,ER阳性乳腺癌占大多数BC亚型。然而,许多最初有反应的BC肿瘤最终会产生获得性他莫昔芬耐药性。对受他莫昔芬影响并在他莫昔芬耐药细胞中上调的基因进行了生物信息学分析,以确定与他莫昔芬耐药相关的生物学过程。进行了代谢组学分析,以确定在对他莫昔芬耐药的BC中发生改变的代谢物。通过体外细胞活力、增殖、侵袭和集落形成以及体内肿瘤生长来评估对他莫昔芬的耐药性。代谢组学分析以及相关酶和代谢物的检测证实了对他莫昔芬耐药的BC中向糖酵解的代谢重编程。产生的乳酸诱导ZMIZ1的乳酰化。K843(而非K537)处的这种翻译后修饰通过抑制SUMO化和泛素化增加了蛋白质稳定性。ZMIZ1总水平的升高增加了ZMIZ1与Nanog结合的富集,导致Nanog转录活性增加,包括在OCT4和NPC2基因中。因此,它导致对他莫昔芬耐药的BC中干性增加和胆固醇积累。敲低ZMIZ1会损害他莫昔芬耐药性,但这种作用会被Nanog过表达逆转。总之,本研究确定了他莫昔芬耐药的一个重要机制,并揭示了通过ZMIZ1/Nanog/NPC2轴葡萄糖糖酵解与胆固醇代谢之间的潜在关联。

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