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小分子抑制剂 HI-TOPK-032 改善 NK-92MI 细胞对卵巢肿瘤的浸润

英文原题:Small-molecule inhibitor HI-TOPK-032 improves NK-92MI cell infiltration into ovarian tumours.

查看英文原题

Small-molecule inhibitor HI-TOPK-032 improves NK-92MI cell infiltration into ovarian tumours.

PubMed 2024/03/19(内容时间) Basic Clin Pharmacol Toxicol Q2 · IF 3.6(JCR 2025)

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中文摘要

自然杀伤(NK)细胞过继转移在对抗实体瘤方面的有效性受到诸多挑战的限制,例如其难以从血流中穿透肿瘤,以及在没有白细胞介素-2(IL-2)支持的情况下难以维持活力。经基因修饰的 NK-92MI 细胞能够释放 IL-2 以维持自身活力,已被认为是一种有前景的替代方案。这一改造解决了全身性 IL-2 给药带来的不良后果。PSD-95/discs large/ZO-1(PDZ)结合激酶(PBK)在癌症发展中的作用已被认识,但其对免疫的影响尚未完全明了。

本研究探讨 PBK 表达如何影响 NK-92MI 细胞浸润卵巢肿瘤的能力。研究发现,包括卵巢癌(OV)在内的多种癌症中 PBK 表达水平升高,分析显示肿瘤组织中 PBK mRNA 水平高于正常组织。免疫组织化学证实 OV 组织中 PBK 表达增加。对 PBK 在免疫调节中作用的研究揭示了其与免疫细胞浸润的关联,表明 PBK 高表达的 OV 中免疫环境可能受损。抑制 PBK 的小分子抑制剂 HI-TOPK-032 可增强 NK-92MI 细胞对 OV 细胞的细胞毒性。它增加干扰素-γ和肿瘤坏死因子-α的产生,减少细胞凋亡并促进细胞增殖。机制研究表明,与经 HI-TOPK-032 处理的 OV 细胞接触后,NK-92 细胞上的 CD107a 表达上调。体内研究表明,HI-TOPK-032 可改善 NK-92MI 细胞在 OVCAR3 Luc 异种移植瘤中的抗肿瘤效果,延长生存期且无明显副作用。小鼠安全性评估证实HI-TOPK-032具有良好的安全性,凸显其作为可行抗肿瘤疗法的潜力。这些结果表明,将NK-92MI细胞与HI-TOPK-032联合使用可增强对OV的抗肿瘤效果,提示这是一种有前景、安全且有效的治疗策略,值得进一步开展临床研究。

展开英文摘要原文

The effectiveness of natural killer (NK) cells transferred adoptively in combating solid tumours is limited by challenges such as their difficulty in penetrating tumours from the bloodstream and maintaining viability without the support of interleukin-2 (IL-2).

Genetically modified NK-92MI cells, which can release IL-2 to sustain their viability, have been identified as a promising alternative. This adaptation addresses the negative consequences of systemic IL-2 administration. The role of PSD-95/discs large/ZO-1 (PDZ)-binding kinase (PBK) in cancer development is recognized, but its effects on immunity are not fully understood.

This study explores how PBK expression influences the ability of NK-92MI cells to infiltrate ovarian tumours. Elevated levels of PBK expression have been found in various cancers, including ovarian cancer (OV), with analyses showing higher PBK mRNA levels in tumour tissues compared to normal ones. Immunohistochemistry has confirmed increased PBK expression in OV tissues. Investigations into PBK's role in immune regulation reveal its association with immune cell infiltration, indicating a potentially compromised immune environment in OV with high PBK expression. The small-molecule inhibitor HI-TOPK-032, which inhibits PBK, enhances the cytotoxicity of NK-92MI cells toward OV cells.

It increases the production of interferon-γ and tumour necrosis factor-α, reduces apoptosis and encourages cell proliferation. Mechanistic studies showed that contact with OV cells treated with HI-TOPK-032 upregulates CD107a on NK-92 cells. In vivo studies demonstrated that HI-TOPK-032 improves the antitumour effects of NK-92MI cells in OVCAR3 Luc xenografts, extending survival without significant side effects.

Safety assessments in mice confirm HI-TOPK-032's favourable safety profile, highlighting its potential as a viable antitumour therapy. These results suggest that combining NK-92MI cells with HI-TOPK-032 enhances antitumour effectiveness against OV, indicating a promising, safe and effective treatment strategy that warrants further clinical investigation.

论文信息

作者
Deng M、Yang R、Sun Q、Zhang J、Miao J
单位
Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing Maternal and Child Health Care Hospital, Beijing, China.China
期刊
Basic & clinical pharmacology & toxicology2024 May
原文标识
PubMed 38501576 · DOI 10.1111/bcpt.14002