Nanomedicine Strategies to Enhance Tumor Drug Penetration in Pancreatic Cancer

被引:14
作者
Lu, Tao [1 ]
Prakash, Jai [1 ]
机构
[1] Univ Twente, Engineered Therapeut Grp, Dept Biomat Sci & Technol, Enschede, Netherlands
关键词
pancreatic ductal adenocarcinoma; cancer-associated fibroblasts; tumor stroma; tumor vasculature; drug perfusion; drug penetration; STELLATE CELLS; MILD HYPERTHERMIA; NAB-PACLITAXEL; GROWTH-FACTOR; MOUSE MODEL; CYCLOOXYGENASE-2; EXPRESSION; DUCTAL ADENOCARCINOMA; CONTROLLED-RELEASE; BREAST-CANCER; LIPOXIN A(4);
D O I
10.2147/IJN.S279192
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Pancreatic cancer is one of the most malignant tumors with one of the worst survival rates due to its insidious onset and resistance to therapies. Most therapeutics show a desired anticancer effect in vitro; however, very poor efficacy in vivo because of the limited drug delivery and penetration into pancreatic tumors attributed to the abundance of the tumor stroma, ie, the fibrotic tumor microenvironment surrounding the cancer cells. For a better understanding of the challenges posed by the pancreatic tumor stroma, we outline the key features of the tumor microenvironment. Then we highlight major strategies used to tackle the challenges to improve drug penetration into the tumor and achieve enhanced efficacy (pre)clinically. Furthermore, we describe nanomedicine strategies to modulate the tumor stroma, degrade the extracellular matrix, and co-deliver multi-functional drugs, to improve the chemotherapeutics delivery and penetration into pancreatic tumors.
引用
收藏
页码:6313 / 6328
页数:16
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