Targeted downregulation of HIF-1α for restraining circulating tumor microemboli mediated metastasis

下调和上调 转移 癌症研究 循环肿瘤细胞 缺氧(环境) 医学 血小板 肿瘤缺氧 体内 缺氧诱导因子 免疫系统 免疫学 癌症 化学 生物 内科学 氧气 放射治疗 生物技术 有机化学 基因 生物化学
作者
Junjie Du,Cong Wang,Yijun Chen,Lingyu Zhong,Xuwentai Liu,Lingjing Xue,Ying Zhang,Yanyi Li,Xiaoyu Li,Chunming Tang,Zhigui Su,Can Zhang
出处
期刊:Journal of Controlled Release [Elsevier BV]
卷期号:343: 457-468 被引量:11
标识
DOI:10.1016/j.jconrel.2022.01.051
摘要

Tumor metastasis is directly correlated to poor prognosis and high mortality. Circulating tumor cells (CTCs) play a pivotal role in metastatic cascades, of which CTC clusters is highly metastatic compared to single CTCs. Although platelets and neutrophils within the bloodstream could further exacerbate the pro-metastatic effect of single CTCs, the influence of platelets and neutrophils on CTC clusters mediated metastasis remains unclear. In this study, a pro-metastatic complex composed of CTC clusters, platelets and neutrophils, namely circulating tumor microemboli (CTM), was identified in vivo among different metastatic tumor, which was demonstrated with highly upregulation of hypoxia-inducible factor-1α (HIF-1α). While knock-out of HIF-1α or therapeutically downregulating of HIF-1α via HIF-1α inhibitor (BAY87-2243)-loaded neutrophil cyto-pharmaceuticals (PNEs) could efficiently restrain CTM mediated lung metastasis. The underlying mechanism of metastasis inhibition was attributed to the downregulation of HIF-1α-associated PD-L1, which would enhance immune response for inhibiting metastatic cells. Thus, our work here illustrates that hypoxia was an essential factor in promoting CTM colonization in lung. More importantly, we provide a promising strategy by targeted downregulation of HIF-1α in CTM via neutrophil cyto-pharmaceuticals for treatment of CTM mediated metastasis.
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