基于 DNA 超分子水凝胶的保护性 NK 细胞储库用于增强三阴性乳腺癌治疗
Protective NK Cell Reservoir Based on DNA Supramolecular Hydrogel for Enhanced Triple-Negative Breast Cancer Therapy.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Combination of oxymatrine (Om) and astragaloside IV (As) enhances the infiltration and function of TILs in triple-negative breast cancer (TNBC).
Combination of oxymatrine (Om) and astragaloside IV (As) enhances the infiltration and function of TILs in triple-negative breast cancer (TNBC).
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三阴性乳腺癌(TNBC)是最具侵袭性的亚型,由于免疫抑制微环境而对治疗反应不佳。中药有效成分如氧化苦参碱(Om)和黄芪甲苷IV(As)通过提供抗纤维化和免疫增强作用,在癌症治疗中显示出前景。
然而,Om和As对TNBC的潜在联合效应及其机制仍不确定。本研究聚焦于探索Om和As对改善TNBC免疫抑制微环境的影响,并揭示其背后的潜在机制。
在本研究中,利用T细胞的跨癌相关成纤维细胞(CAFs)浸润系统来研究Om的潜在益处,同时在肿瘤细胞共培养系统中检测As对T细胞线粒体形态和数量的影响。为进一步研究Om和As对肿瘤抑制和免疫抑制微环境改善的联合效应,本研究建立了4 T1-luc原位TNBC小鼠模型。在体外,我们的发现表明Om可通过下调FAP和α-SMA的表达有效抑制CAFs的活化,并促进T细胞跨CAFs浸润。
研究发现,通过增加线粒体数量和嵴的数量,可改善T细胞的线粒体活性。在体内,发现Om和As的最佳比例(2:1)可增加共培养系统中肿瘤细胞的凋亡率,并增强CD4 + 和CD8 + T细胞的浸润,流式细胞术结果证实了这一点。
我们的研究表明,Om和As可能通过改善TILs的浸润和增强其抗肿瘤功能,来增强免疫系统治疗TNBC的能力。这一干预措施可能为TNBC的治疗带来一个有前景的治疗方向。
Triple-negative breast cancer (TNBC) is the most aggressive subtype and has a poor response to treatment due to an immunosuppressive microenvironment. Chinese Medicine effective constituents such as oxymatrine (Om) and astragaloside IV (As) have shown promise in cancer treatment by providing anti-fibrosis and immune-enhancing effects.
However, the potential combined effect of Om and As on TNBC and its mechanism is still uncertain.
This study focuses on exploring the impact of Om and As on enhancing the immunosuppressive microenvironment of TNBC and uncovering the potential mechanism behind it. In this study, a trans-Cancer associated fibroblasts (CAFs) infiltration system of T cells was utilized to investigate the potential benefits of Om, while the impact of As on the morphology and quantity of mitochondria in T cells was examined in a co-culture system with tumor cells.
Further to investigate the combined effects of Om and As on tumor suppression and immunosuppressive microenvironment improvement, this study established an in situ TNBC mouse model with 4 T1-luc. In vitro, our findings indicate that Om can effectively suppress the activation of CAFs by downregulating the expression of FAP and α-SMA, and also promoting the infiltration of T cells trans CAFs.
It was discovered that the mitochondrial activity of T cells could be improved by increasing the number of mitochondria and cristae. In vivo, the optimal ratio of Om and As (2:1) was found to increase the apoptosis rate of tumor cells in a co-culture system and enhance the infiltration of CD4 + and CD8 + T cells, as confirmed by Flow Cytometry results.
Our study suggests that Om and As could enhance the immune system's ability to treat TNBC by improving the infiltration and increasing the anti-tumor function of TILs. This intervention may lead to a promising therapeutic direction for the treatment of TNBC.
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