紫杉醇
卵巢癌
脂解
体内
癌症研究
细胞
癌细胞
癌症
药物输送
体外
细胞生长
肿瘤微环境
脂肪组织
生物
医学
药理学
化学
内科学
生物化学
生物技术
有机化学
作者
Pacome K. Andele,Stefano Palazzolo,Giuseppe Corona,Isabella Caligiuri,Urška Kamenšek,Maja Čemažar,Vincenzo Canzonieri,Flavio Rizzolio
标识
DOI:10.1002/adhm.202304206
摘要
Primary human omental adipocytes and ovarian cancer(OC) cells establish a bidirectional communication in which tumor driven lipolysis is induced in adipocytes and the resulting fatty acids are delivered to cancer cells within the tumor microenvironment. Despite meaningful improvement in the treatment of OC, its efficacy is still limited by hydrophobicity and untargeted effects related to chemotherapeutics. Herein, omental adipocytes are firstly used as a reservoir for paclitaxel, named Living Paclitaxel Bullets (LPB) and secondly benefit from the established dialogue between adipocytes and cancer cells to engineer a drug delivery process that target specifically cancer cells. These results show that mature omental adipocytes can successfully uptake paclitaxel and deliver it to OC cells in a transwell coculture based in vitro model. In addition, the efficacy of this proof-of-concept has been demonstrated in vivo and induces a significant inhibition of tumor growth on a xenograft tumor model. The use of mature adipocytes can be suitable for clinical prospection in a cell-based therapy system, due to their mature and differentiated state, to avoid risks related to uncontrolled cell de novo proliferation capacity after the delivery of the antineoplastic drug as observed with other cell types when employed as drug carriers.
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