基质
肿瘤微环境
结缔组织增生
胰腺癌
癌症研究
间质细胞
转移
癌细胞
化学
吉西他滨
药物输送
紫杉醇
癌症
胰腺肿瘤
纳米载体
材料科学
体内
光热治疗
生物
医学
免疫学
肿瘤细胞
内科学
免疫组织化学
有机化学
作者
Han Y. H. Chen,Wenxi Zhou,Chen Liang,Si Shi,Xianjun Yu,Qinjun Chen,Tao Sun,Yifei Lü,Yujie Zhang,Qin Guo,Chao Li,Yu Zhang,Chen Jiang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2019-05-06
卷期号:19 (6): 3527-3534
被引量:53
标识
DOI:10.1021/acs.nanolett.9b00374
摘要
Pancreatic ductal adenocarcinoma (PDAC) is considered as one of the most aggressive malignancies due to its unique microenvironment of which the cardinal histopathological feature is the remarkable desmoplasia of the stroma, taking up about 80% of the tumor mass. The desmoplastic stroma negatively affects drug diffusion and the infiltration of T cells, leading to an immunosuppressive microenvironment. However, this unique microenvironment can limit the physical spread of pancreatic cancer via a neighbor suppression effect. Here, a tumor central stroma targeting and microenvironment responsive strategy was applied to generate a nanoparticle coloading paclitaxel and phosphorylated gemcitabine. The designed nanoparticle disrupted the central stroma while preserving the external stroma, thereby promoting the antitumor effectiveness of chemotherapeutics. Additionally, the resulting nanoparticle can modulate the tumor immunosuppressive microenvironment by augmenting the number of cytotoxic T cells and restraining the percentage of T regulatory cells. The relatively intact external stroma can effectively maintain the neighbor suppression effect and prevent tumor metastasis. Combining stroma targeting with the delivery of stimuli-responsive polymeric nanoparticles embodies an effective tumor-tailored drug delivery system.
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