Перейти к основному содержанию
AkademIndex

Продукты

Для разработчиков

AkademBaseОткрытый API экосистемы
Статья

Reprogramming Tumor Immune Microenvironment (TIME) and Metabolism via Biomimetic Targeting Codelivery of Shikonin/JQ1

Hairui WangInstitute of Tropical Medical, Guangzhou University of Chinese Medicine, 12 Jichang Road, Guangzhou 510450, ChinaYisi TangInstitute of Tropical Medical, Guangzhou University of Chinese Medicine, 12 Jichang Road, Guangzhou 510450, ChinaYuefei FangInstitute of Tropical Medical, Guangzhou University of Chinese Medicine, 12 Jichang Road, Guangzhou 510450, ChinaMeng ZhangState Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 501 Haike Road, Shanghai 201203, ChinaHuiyuan WangInstitute of Tropical Medical, Guangzhou University of Chinese Medicine, 12 Jichang Road, Guangzhou 510450, ChinaZhidi HeState Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 501 Haike Road, Shanghai 201203, ChinaBing WangState Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 501 Haike Road, Shanghai 201203, ChinaQin XuInstitute of Tropical Medical, Guangzhou University of Chinese Medicine, 12 Jichang Road, Guangzhou 510450, ChinaYongzhuo HuangState Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 501 Haike Road, Shanghai 201203, China
2019en
ABI

Аннотация

Remodeling tumor immune microenvironment (TIME) is an important strategy to lift the immunosuppression and achieve immune normalization. In this work, a mannosylated lactoferrin nanoparticulate system (Man-LF NPs) is developed for dual-targeting biomimetic codelivery of shikonin and JQ1 via the mannose receptor and LRP-1 that are overexpressed in both cancer cells and tumor-associated macrophages. The Man-LF NPs can serve as multitarget therapy for inducing immune cell death in the cancer cells, repressing glucose metabolism and repolarizing tumor-associated macrophages, and consequently, lead to remodeling the TIME (e.g., promotion of dendritic cell maturation and CD8+ T cell infiltration, as well as suppression of Treg). Moreover, JQ1 is a suppressor of PD-L1, and the Man-LF NPs can also work on PD-L1 checkpoint blockage. The results reveal the synergistic combination of shikonin and JQ1 and the treatment potency of the Man-LF NPs. Importantly, it is demonstrated that the interaction between the tumor metabolism and immunity plays an essential role in immunotherapy, and the developed drug combination and nanoformulation can target the multiple components in the complicated network of TIME, providing a potential therapeutic strategy.

Перевод пока недоступен

Идентификаторы

Цитирования и источники

Цитирований: 4Использованных источников: 0