tLyp-1-EV-shCTCF 通过调节 SALL3 抑制肝癌干细胞自我更新和免疫逃逸的治疗潜力

IF 5 2区 医学 Q2 Medicine Translational Oncology Pub Date : 2024-08-25 DOI:10.1016/j.tranon.2024.102048
Heng Zhu , Zhihui Xie
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引用次数: 0

摘要

肝细胞癌(HCC)的进展受代谢过程紊乱的影响,给预后结果带来了挑战。肝细胞癌(HCC)是癌症相关死亡的主要原因,它与肝癌干细胞(LCSCs)的代谢重编程和干细胞样特性密切相关。本研究探索了tLyP-1修饰的细胞外囊泡递送CTCF shRNA(tLyp-1-EV-shCTCF)调控线粒体DNA甲基化诱导的糖酵解代谢重编程和LCSC自我更新的潜在分子机制。通过Western印迹、纳米颗粒追踪分析和免疫荧光等一系列方法,我们证明了tLyp-1-EV在HCC细胞中的成功递送和内化。我们的研究结果发现,SALL3 是 HCC 和 LCSCs 中表达不足的关键因子,而 CTCF 则表达过高。SALL3 的过表达通过阻断 CTCF-DNMT3A 的相互作用抑制了 LCSC 的自我更新和免疫逃避,从而抑制了 DNMT3A 甲基转移酶的活性以及随后线粒体 DNA 甲基化介导的糖酵解代谢重编程。体内实验进一步支持了这些发现,实验结果表明,tLyp-1-EV-shCTCF 治疗通过上调 SALL3 的表达,从而抑制了糖酵解代谢重编程,增强了针对 HCC 细胞的免疫反应,从而显著降低了肿瘤的生长。这项研究为SALL3和线粒体DNA甲基化在HCC进展中的作用提供了新的见解,为抗击HCC及其干细胞样特性提供了潜在的治疗靶点。
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Therapeutic potential of tLyp-1-EV-shCTCF in inhibiting liver cancer stem cell self-renewal and immune escape via SALL3 modulation in hepatocellular carcinoma

The progression of hepatocellular carcinoma (HCC) is influenced by disrupted metabolic processes, presenting challenges in prognostic outcomes. Hepatocellular carcinoma (HCC), a leading cause of cancer-related mortality, is closely associated with metabolic reprogramming and stem cell-like properties in liver cancer stem cells (LCSCs). This study explored the potential molecular mechanisms by which tLyP-1-modified extracellular vesicles (EVs) delivering CTCF shRNA (tLyp-1-EV-shCTCF) regulate mitochondrial DNA methylation-induced glycolytic metabolic reprogramming and LCSC self-renewal. Through a series of methods, including Western blot, nanoparticle tracking analysis, and immunofluorescence, we demonstrated the successful delivery and internalization of tLyp-1-EV in HCC cells. Our results identified SALL3 as a critical factor underexpressed in HCC and LCSCs, while CTCF was overexpressed. Overexpression of SALL3 inhibited LCSC self-renewal and immune evasion by blocking the CTCF-DNMT3A interaction, thus repressing DNMT3A methyltransferase activity and subsequent mitochondrial DNA methylation-mediated glycolytic metabolic reprogramming. In vivo experiments further supported these findings, showing that tLyp-1-EV-shCTCF treatment significantly reduced tumor growth by upregulating SALL3 expression, thereby inhibiting glycolytic metabolic reprogramming and enhancing the immune response against HCC cells. This study provides novel insights into the role of SALL3 and mitochondrial DNA methylation in HCC progression, offering potential therapeutic targets for combating HCC and its stem cell-like properties.

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来源期刊
CiteScore
8.40
自引率
2.00%
发文量
314
审稿时长
54 days
期刊介绍: Translational Oncology publishes the results of novel research investigations which bridge the laboratory and clinical settings including risk assessment, cellular and molecular characterization, prevention, detection, diagnosis and treatment of human cancers with the overall goal of improving the clinical care of oncology patients. Translational Oncology will publish laboratory studies of novel therapeutic interventions as well as clinical trials which evaluate new treatment paradigms for cancer. Peer reviewed manuscript types include Original Reports, Reviews and Editorials.
期刊最新文献
Clinical efficacies of different neoadjuvant therapies for non-small cell lung cancer Integrated multi-omics demonstrates enhanced antitumor efficacy of donafenib combined with FADS2 inhibition in hepatocellular carcinoma Disruption of bioenergetics enhances the radio-sensitivity of patient-derived glioblastoma tumorspheres KRas plays a negative role in regulating IDO1 expression Comparative transcriptomic analysis uncovers molecular heterogeneity in hepatobiliary cancers
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