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木犀草素作为佐剂可有效增强过继性肿瘤特异性细胞毒性T淋巴细胞(CTLs)疗法的疗效。

Luteolin as an adjuvant effectively enhanced the efficacy of adoptive tumor-specific CTLs therapy.

作者信息

Lai Zhiheng, Pang Yanyang, Zhou Yujing, Chen Leiyuan, Zheng Kai, Yuan Shiguo, Wang Wu

机构信息

Department of Anorectal Surgery, Hainan Traditional Chinese Medicine Hospital, Hainan Medical University, Haikou, China.

Department of Anorectal Surgery, Hainan Hospital, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou University of Chinese Medicine, Guangzhou, China.

出版信息

BMC Cancer. 2025 Mar 6;25(1):411. doi: 10.1186/s12885-025-13831-8.

Abstract

BACKGROUND

Luteolin, a natural flavonoid compound, has demonstrated anti-inflammatory, antioxidant, and broad anti-tumor properties. Recent studies suggest that its anti-tumor effects are linked to enhanced CTL function-including proliferation, survival, and cytotoxicity-via inhibition of the YAP/Wnt signaling pathway in tumor cells. Consequently, luteolin has potential as an adjuvant in combination therapies with adoptive immunotherapy.

METHODS

This study first assessed luteolin's tumor-inhibitory effects in vitro and in vivo using cytotoxicity assays, Transwell invasion tests, wound healing assays, and analyses of post-treatment tumor growth and survival time. Additionally, we explored whether luteolin combined with a DC/tumor fusion vaccine could synergistically enhance overall antitumor efficacy by boosting activation, proliferation, cytokines secretion, and cytotoxicity of effector T cells.

RESULTS

Our findings indicate that luteolin, as a standalone agent, can inhibit the proliferation and invasion of colon and lung cancer cells both in vitro and in vivo to a certain extent. When combined with activated CTLs, it upregulated the expression of CD25 and CD69 in effector cells and resulted in higher levels of IL-2, TNF-α, and IFN-γ secretion in vitro. In vivo, this combination significantly curtailed subcutaneous tumor growth and extended the mean survival time of tumor-bearing mice (HCT116, A549), outperforming luteolin monotherapy. Furthermore, the efficacy of this combination therapy may be attributable to enhanced apoptosis in tumor cells, reduced proliferation, and decreased YAP expression.

CONCLUSION

The combination of luteolin and DC/tumor fusion vaccine-activated CTLs presents a novel approach for cancer treatment. As an adjuvant, luteolin downregulates YAP expression in tumor cells, enhancing CTL proliferation, cytotoxicity, and survival, thus improving tumor recognition and selective targeting. This strategy is promising for safe and effective tumor treatment.

摘要

背景

木犀草素是一种天然黄酮类化合物,已显示出抗炎、抗氧化和广泛的抗肿瘤特性。最近的研究表明,其抗肿瘤作用与通过抑制肿瘤细胞中的YAP/ Wnt信号通路增强CTL功能(包括增殖、存活和细胞毒性)有关。因此,木犀草素在与过继性免疫疗法的联合治疗中具有作为佐剂的潜力。

方法

本研究首先使用细胞毒性试验、Transwell侵袭试验、伤口愈合试验以及治疗后肿瘤生长和存活时间分析,在体外和体内评估木犀草素的肿瘤抑制作用。此外,我们探讨了木犀草素与DC/肿瘤融合疫苗联合使用是否可以通过增强效应T细胞的激活、增殖、细胞因子分泌和细胞毒性来协同提高整体抗肿瘤疗效。

结果

我们的研究结果表明,木犀草素作为单一药物,在体外和体内均可在一定程度上抑制结肠和肺癌细胞的增殖和侵袭。与活化的CTL联合使用时,它上调了效应细胞中CD25和CD69的表达,并导致体外IL-2、TNF-α和IFN-γ分泌水平升高。在体内,这种联合显著抑制了皮下肿瘤生长,并延长了荷瘤小鼠(HCT116、A549)的平均存活时间,优于木犀草素单药治疗。此外,这种联合治疗的疗效可能归因于肿瘤细胞凋亡增加、增殖减少和YAP表达降低。

结论

木犀草素与DC/肿瘤融合疫苗激活的CTL联合使用为癌症治疗提供了一种新方法。作为佐剂,木犀草素下调肿瘤细胞中的YAP表达,增强CTL增殖、细胞毒性和存活,从而改善肿瘤识别和选择性靶向。这种策略有望实现安全有效的肿瘤治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0d0/11887225/a1e3ff9a58d0/12885_2025_13831_Fig1_HTML.jpg

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