Inhibiting collagen Ⅰ production and tumor cell colonization in the lung via miR-29a-3p loading of exosome-/liposome-based nanovesiclesOA

作者：Yan Yan; Cancan Du; Xixi Duan; Xiaohan Yao; Jiajia Wan; Ziming Jiang; Zhongyu Qin; Wenqing Li; Longze Pan; Zhuoyu Gu; Fazhan Wang^*; Ming Wang^*; Zhihai Qin^*

来源：Acta Pharmaceutica Sinica B, 2022, 12(02): 939-951.

The lung is one of the most common sites for cancer metastasis. Collagens in the lung provide a permissive microenvironment that supports the colonization and outgrowth of disseminated tumor cells. Therefore, down-regulating the production of collagens may contribute to the inhibition of lung metastasis. It has been suggested that mi R-29 exhibits effective anti-fibrotic activity by negatively regulating the expression of collagens. Indeed, our clinical lung tumor data shows that mi R-29 a-3 p expression negatively correlates with collagen I expression in lung tumors and positively correlates with patients’ outcomes. However, suitable carriers need to be selected to deliver this therapeutic mi RNA to the lungs.In this study, we found that the chemotherapy drug cisplatin facilitated mi R-29 a-3 p accumulation in the exosomes of lung tumor cells, and this type of exosomes exhibited a specific lung-targeting effect and promising collagen down-regulation. To scale up the preparation and simplify the delivery system, we designed a lung-targeting liposomal nanovesicle(by adjusting the molar ratio of DOTAP/cholesterol -mi RNAs to 4:1) to carry mi R-29 a-3 p and mimic the exosomes. This liposomal nanovesicle delivery system significantly down-regulated collagen I secretion by lung fibroblasts in vivo, thus alleviating the establishment of a pro-metastatic environment for circulating lung tumor cells.

• 单位
  郑州大学