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Anti-angiogenic and anti-tumor effects of metronomic use of novel liposomal zoledronic acid depletes tumor-associated macrophages in triple negative breast cancer

机译:新型脂质体唑来膦酸的基因组使用的抗血管生成和抗肿瘤作用可消除三阴性乳腺癌中与肿瘤相关的巨噬细胞

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摘要

Zoledronic acid (ZOL) has been used as an adjuvant therapy for breast cancer. It is suggested that ZOL might be associated with inhibition of macrophages, which in turn reduces tumor growth, metastasis and tumor angiogenesis. Moreover, metronomic therapy can inhibit tumor angiogenesis and tumor immune cells. Previously we developed ZOL based cationic liposomes that allowed a higher intratumor delivery of drug compared with free ZOL in vivo. Therefore, in this study, Asn-Gly-Arg (NGR) and PEG2000 were used as ligands to modify the surface of liposomes (NGR-PEG-LP-ZOL) in metronomic therapy to clear the tumor-associated macrophages (TAMs) and inhibit the formation of tumor angiogenesis, achieving the purpose of anti-tumor growth.Our data showed that NGR-PEG-LP-ZOL metronomic therapy has the strongest inhibitory effect on tumor growth. Further, NGR-PEG-LP-ZOL metronomic therapy could significantly impair TAMs by inhibiting the expression of CD206 antibody in tumor tissues, decreasing the expression of cytokine related gene expression of TAMs, as well as reducing the percentage of TAMs in tumor tissues. In addition, NGR-PEG-LP-ZOL metronomic therapy could significantly inhibit the expression of tumor neovascular specific antibody CD31 and reduce the microvessel density. In conclusion, our study demonstrated that NGR-PEG-LP-ZOL metronomic therapy could impair TAMs by inhibiting tumor angiogenesis and enhance the antitumor effect of ZOL.
机译:唑来膦酸(ZOL)已被用作乳腺癌的辅助疗法。提示ZOL可能与巨噬细胞的抑制有关,这反过来减少了肿瘤的生长,转移和肿瘤的血管生成。此外,节拍疗法可以抑制肿瘤血管生成和肿瘤免疫细胞。以前,我们开发了基于ZOL的阳离子脂质体,与游离ZOL体内相比,该脂质体可实现更高的肿瘤内药物递送。因此,在这项研究中,Asn-Gly-Arg(NGR)和PEG2000被用作配体,以在基因组治疗中修饰脂质体(NGR-PEG-LP-ZOL)的表面,以清除肿瘤相关的巨噬细胞(TAM)并抑制我们的数据表明,NGR-PEG-LP-ZOL节律疗法对肿瘤的生长具有最强的抑制作用。此外,NGR-PEG-LP-ZOL节律疗法可通过抑制肿瘤组织中CD206抗体的表达,降低TAMs的细胞因子相关基因表达以及减少肿瘤组织中TAM的百分比来显着损害TAM。此外,NGR-PEG-LP-ZOL节律疗法可显着抑制肿瘤新血管特异性抗体CD31的表达并降低微血管密度。总之,我们的研究表明NGR-PEG-LP-ZOL节律疗法可通过抑制肿瘤血管生成并增强ZOL的抗肿瘤作用来损害TAM。

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