Extensive Review of Nanomedicine Strategies Targeting the Tumor Microenvironment in PDAC

被引:3
作者
Liu, Xing [1 ]
Shao, Yidan [2 ]
Li, Yunjiang [3 ]
Chen, Zuhua [3 ]
Shi, Tingting [2 ]
Tong, Qiao [2 ]
Zou, Xi [2 ]
Ju, Liping [2 ]
Pan, Jinming [2 ]
Zhuang, Rangxiao [2 ]
Pan, Xuwang [2 ]
机构
[1] Zhejiang Chinese Med Univ, Sch Pharmaceut Sci, Hangzhou 311400, Zhejiang, Peoples R China
[2] Zhejiang Chinese Med Univ, Affiliated Hangzhou Xixi Hosp, Dept Pharmaceut Preparat, 2 Hengbu Rd, Hangzhou 310023, Zhejiang, Peoples R China
[3] Zhejiang Chinese Med Univ, Affiliated Hangzhou Xixi Hosp, Radiol Dept, Hangzhou 310023, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
nanoscale; drug delivery systems; pancreatic ductal adenocarcinoma; tumor microenvironment; deep penetration; PANCREATIC-CANCER MICROENVIRONMENT; POLYMERIC MIXED MICELLES; DRUG-DELIVERY; TRANSFERRIN RECEPTOR; NANOPARTICLES; GEMCITABINE; THERAPY; CHECKPOINT; ADHESION; SYSTEM;
D O I
10.2147/IJN.S504503
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Pancreatic ductal adenocarcinoma (PDAC) is one of the deadliest cancers in the world, mainly because of its powerful proconnective tissue proliferation matrix and immunosuppressive tumor microenvironment (TME), which promote tumor progression and metastasis. In addition, the extracellular matrix leads to vascular collapse, increased interstitial fluid pressure, and obstruction of lymphatic return, thereby hindering effective drug delivery, deep penetration, and immune cell infiltration. Therefore, reshaping the TME to enhance tumor perfusion, increase deep drug penetration, and reverse immune suppression has become a key therapeutic strategy. Traditional therapies for PDAC, including surgery, radiation, and chemotherapy, face significant limitations. Surgery is challenging due to tumor location and growth, while chemotherapy and radiation are hindered by the dense extracellular matrix and immunosuppressive TME. In recent years, the advancement of nanotechnology has provided new opportunities to improve drug efficacy. Nanoscale drug delivery systems (NDDSs) provide several advantages, including improved drug stability in vivo, enhanced tumor penetration, and reduced systemic toxicity. However, the clinical translation of nanotechnology in PDAC therapy faces several challenges. These include the need for precise targeting and control over drug release, potential immune responses to the nanocarriers, and the scalability and cost-effectiveness of production. This article provides an overview of the latest nanobased methods for achieving better therapeutic outcomes and overcoming drug resistance. We pay special attention to TME-targeted therapy in the context of PDAC, discuss the advantages and limitations of current strategies, and emphasize promising new developments. By emphasizing the enormous potential of NDDSs in improving the treatment outcomes of patients with PDAC, while critically discussing the limitations of traditional therapies and the challenges faced by nanotechnology in achieving clinical breakthroughs, our review paves the way for future research in this rapidly developing field.
引用
收藏
页码:3379 / 3406
页数:28
相关论文
共 149 条
[51]   Stroma-Targeting Therapy in Pancreatic Cancer: One Coin With Two Sides? [J].
Jiang, Bolun ;
Zhou, Li ;
Lu, Jun ;
Wang, Yizhi ;
Liu, Chengxi ;
You, Lei ;
Guo, Junchao .
FRONTIERS IN ONCOLOGY, 2020, 10
[52]   Pancreatic ductal adenocarcinoma progression is restrained by stromal matrix [J].
Jiang, Honglin ;
Torphy, Robert J. ;
Steiger, Katja ;
Hongo, Henry ;
Ritchie, Alexa J. ;
Kriegsmann, Mark ;
Horst, David ;
Umetsu, Sarah E. ;
Joseph, Nancy M. ;
McGregor, Kimberly ;
Pishvaian, Michael J. ;
Blais, Edik M. ;
Lu, Brian ;
Li, Mingyu ;
Hollingsworth, Michael ;
Stashko, Connor ;
Volmar, Keith ;
Yeh, Jen Jen ;
Weaver, Valerie M. ;
Wang, Zhen J. ;
Tempero, Margaret A. ;
Weichert, Wilko ;
Collisson, Eric A. .
JOURNAL OF CLINICAL INVESTIGATION, 2020, 130 (09) :4704-4709
[53]  
Jiang S, 2022, AGING-US, V14, P7635, DOI 10.18632/aging.204310
[54]   The uPA/uPAR System Orchestrates the Inflammatory Response, Vascular Homeostasis, and Immune System in Fibrosis Progression [J].
Kanno, Yosuke .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2023, 24 (02)
[55]   CD44-Targeted Nanocarrier for Cancer Therapy [J].
Kesharwani, Prashant ;
Chadar, Rahul ;
Sheikh, Afsana ;
Rizg, Waleed Y. ;
Safhi, Awaji Y. .
FRONTIERS IN PHARMACOLOGY, 2022, 12
[56]   Arsenic trioxide and Erlotinib loaded in RGD-modified nanoliposomes for targeted combination delivery to PC3 and PANC-1 cell lines [J].
Khosravani, Fatemeh ;
Mir, Hamed ;
Mirzaei, Ali ;
Kobarfard, Farzad ;
Bardania, Hassan ;
Hosseini, Ebrahim .
BIOTECHNOLOGY AND APPLIED BIOCHEMISTRY, 2023, 70 (02) :811-823
[57]   Expression of urokinase-type plasminogen activator system in non-metastatic prostate cancer [J].
Kimura, Shoji ;
D'Andrea, David ;
Iwata, Takehiro ;
Foerster, Beat ;
Janisch, Florian ;
Parizi, Mehdi Kardoust ;
Moschini, Marco ;
Briganti, Alberto ;
Babjuk, Marko ;
Chlosta, Piotr ;
Karakiewicz, Pierre, I ;
Enikeev, Dmitry ;
Rapoport, Leonid M. ;
Seebacher, Veronica ;
Egawa, Shin ;
Abufaraj, Mohammad ;
Shariat, Shahrokh F. .
WORLD JOURNAL OF UROLOGY, 2020, 38 (10) :2501-2511
[58]   Pancreatic cancer: Stroma and its current and emerging targeted therapies [J].
Kota, Janaiah ;
Hancock, Julie ;
Kwon, Jason ;
Korc, Murray .
CANCER LETTERS, 2017, 391 :38-49
[59]   The Urokinase Plasminogen Activation System in Pancreatic Cancer: Prospective Diagnostic and Therapeutic Targets [J].
Kumar, Ashna A. ;
Buckley, Benjamin J. ;
Ranson, Marie .
BIOMOLECULES, 2022, 12 (02)
[60]   Targeted Co-delivery of the Iron Chelator Deferoxamine and a HIF1α Inhibitor Impairs Pancreatic Tumor Growth [J].
Lang, Jiayan ;
Zhao, Xiao ;
Wang, Xiuchao ;
Zhao, Ying ;
Li, Yiye ;
Zhao, Ruifang ;
Cheng, Keman ;
Li, Yao ;
Han, Xuexiang ;
Zheng, Xiaowei ;
Qin, Hao ;
Geranpayehvaghei, Marzieh ;
Shi, Jian ;
Anderson, Gregory J. ;
Hao, Jihui ;
Ren, He ;
Nie, Guangjun .
ACS NANO, 2019, 13 (02) :2176-2189