通过表没食子儿茶素-3-没食子酸酯协同增强奥西替尼对非小细胞肺癌细胞的疗效:YAP/TEAD/CTGF轴抑制的机制

IF 4.1 Q2 PHARMACOLOGY & PHARMACY
Advanced pharmaceutical bulletin Pub Date : 2025-03-23 eCollection Date: 2025-07-01 DOI:10.34172/apb.43809
Ashwini Somayaji, Chakrakodi Shashidhara Shastry
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引用次数: 0

摘要

目的:联合治疗对于治疗晚期非小细胞肺癌(NSCLC)至关重要,特别是克服对第三代表皮生长因子受体(EGFR)如奥西替尼(OSI)的耐药。Hippo信号通路是细胞增殖、凋亡和肿瘤进展的关键调节因子,在非小细胞肺癌中经常失调,并有助于化疗耐药。本研究研究了绿茶多酚表没食子儿茶素-3-没食子酸酯(EGCG)通过调节Hippo信号通路,特别是通过抑制YAP-1 (es相关蛋白)-TEAD (tea结构域转录因子)-CTGF(结缔组织生长因子)轴来克服OSI抗性的潜力。方法:采用逐步剂量递增的方法,从EGFR t790m突变的H460细胞中培养抗osi (OR)克隆。评估EGCG的抗增殖作用,并使用组合指数(CI)值和中位效应概念分析OSI和EGCG之间的协同相互作用。机制研究评估了联合治疗对Hippo信号通路的影响,重点是对YAP/TEAD/CTGF信号轴的抑制。结果:OR克隆的OSI IC50值(25.12 ~ 28.48µM)明显高于亲本H460细胞(2.74±0.2µM)。EGCG处理以浓度依赖性方式降低细胞活力,H460细胞的IC50值为102.54±0.23μM, OR克隆的IC50值为225.79 ~ 237.36µM。OSI和EGCG联合处理在1:2摩尔比下表现出很强的协同作用,CI值表明在IC50至IC95范围内的协同作用。在机制上,共处理抑制了YAP/TEAD/CTGF轴的过表达,恢复了Hippo通路活性,逆转了OSI抗性。结论:本研究提供了EGCG有效靶向Hippo信号通路克服非小细胞肺癌OSI耐药的证据。将EGCG纳入联合治疗有望成为对抗治疗耐药和改善egfr突变NSCLC患者预后的新方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Synergistic Enhancement of Osimertinib Efficacy in Non-small Cell Lung Cancer Cells Through Epigallocatechin-3-Gallate: Mechanistic Insights Into YAP/TEAD/CTGF Axis Inhibition.

Synergistic Enhancement of Osimertinib Efficacy in Non-small Cell Lung Cancer Cells Through Epigallocatechin-3-Gallate: Mechanistic Insights Into YAP/TEAD/CTGF Axis Inhibition.

Synergistic Enhancement of Osimertinib Efficacy in Non-small Cell Lung Cancer Cells Through Epigallocatechin-3-Gallate: Mechanistic Insights Into YAP/TEAD/CTGF Axis Inhibition.

Synergistic Enhancement of Osimertinib Efficacy in Non-small Cell Lung Cancer Cells Through Epigallocatechin-3-Gallate: Mechanistic Insights Into YAP/TEAD/CTGF Axis Inhibition.

Purpose: Combinatorial therapies are essential for treating advanced non-small cell lung cancer (NSCLC), particularly overcoming resistance to third-generation epidermal growth factor receptor (EGFR) like osimertinib (OSI). The Hippo signaling pathway, a critical regulator of cell proliferation, apoptosis, and tumor progression, is often dysregulated in NSCLC and contributes to chemo-resistance. This study investigated the potential of epigallocatechin-3-gallate (EGCG), a green tea polyphenol, to overcome OSI resistance by modulating the Hippo signaling pathway, specifically through inhibition of the YAP-1 (Yes-associated protein)-TEAD (TEA domain transcription factor)-CTGF (connective tissue growth factor) axis.

Methods: Using stepwise dose escalation, OSI-resistant (OR) clones were developed from EGFR T790M-mutated H460 cells. The anti-proliferative effects of EGCG were assessed, and synergistic interactions between OSI and EGCG were analysed using combination index (CI) values and the median effect concept. Mechanistic studies evaluated the co-treatment's impact on the Hippo signaling pathway, focusing on the inhibition of the YAP/TEAD/CTGF signaling axis.

Results: The OR clones exhibited significantly higher IC50 values for OSI (25.12-28.48 µM) compared to parental H460 cells (2.74±0.2µM). EGCG treatment reduced cell viability in a concentration-dependent manner, with IC50 values of 102.54±0.23μM for H460 cells and 225.79-237.36 µM for OR clones. Combination treatment of OSI and EGCG showed strong synergy at a 1:2 molar ratio, with CI values indicating synergism across a range from IC50 to IC95. Mechanistically, co-treatment suppressed the overexpression of the YAP/TEAD/CTGF axis, restoring Hippo pathway activity and reversing OSI resistance.

Conclusion: This study provides evidence that EGCG effectively targets the Hippo signaling pathway to overcome OSI resistance in NSCLC. The inclusion of EGCG in combinatorial therapies holds promise as a novel approach to combat therapeutic resistance and improve outcomes for patients with EGFR-mutated NSCLC.

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来源期刊
Advanced pharmaceutical bulletin
Advanced pharmaceutical bulletin PHARMACOLOGY & PHARMACY-
CiteScore
6.80
自引率
2.80%
发文量
51
审稿时长
12 weeks
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