Nanomedicine approaches for treatment of hematologic and oncologic malignancies

被引:3
作者
Nteli, Polyxeni [1 ]
Bajwa, Danae Efremia [1 ]
Politakis, Dimitrios [1 ]
Michalopoulos, Charalampos [1 ]
Kefala-Narin, Anastasia [1 ]
Efstathopoulos, Efstathios P. [2 ]
Gazouli, Maria [1 ,3 ]
机构
[1] Natl & Kapodistrian Univ Athens, Med Sch, Dept Basic Med Sci, Athens 11527, Greece
[2] Natl & Kapodistrian Univ Athens, Gen Univ Hosp Attikon, Med Sch, Dept Radiol 2, Athens 12462, Greece
[3] Natl & Kapodistrian Univ Athens, Med Sch, Dept Basic Med Sci, Michalakopoulou 176, Athens 11527, Greece
关键词
Nanomedicine; Cancer; Immunotherapy; Gene; Cell therapy; CHEMICAL-MODIFICATIONS; NANOPARTICLE DELIVERY; PD-L1; EXPRESSION; CANCER; IMMUNOTHERAPY; RNA; FUTURE; PEMBROLIZUMAB; STRATEGIES; HALLMARKS;
D O I
10.5306/wjco.v13.i7.553
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer is a leading cause of death worldwide. Nowadays, the therapies are inadequate and spur demand for improved technologies. Rapid growth in nanotechnology and novel nanomedicine products represents an opportunity to achieve sophisticated targeting strategies and multi-functionality. Nanomedicine is increasingly used to develop new cancer diagnosis and treatment methods since this technology can modulate the biodistribution and the target site accumulation of chemotherapeutic drugs, thereby reducing their toxicity. Cancer nanotechnology and cancer immunotherapy are two parallel themes that have emerged over the last few decades while searching for a cure for cancer. Immunotherapy is revolutionizing cancer treatment, as it can achieve unprecedented responses in advanced-stage patients, including complete cures and long-term survival. A deeper understanding of the human immune system allows the establishment of combination regimens in which immunotherapy is combined with other treatment modalities (as in the case of the nanodrug Ferumoxytol). Furthermore, the combination of gene therapy approaches with nanotechnology that aims to silence or express cancer-relevant genes via one-time treatment is gradually progressing from bench to bedside. The most common example includes lipid-based nanoparticles that target VEGF-& UAlpha; and KRAS pathways. This review focuses on nanoparticle-based platforms utilized in recent advances aiming to increase the efficacy of currently available cancer therapies. The insights provided and the evidence obtained in this paper indicate a bright future ahead for immuno-oncology applications of engineering nanomedicines.
引用
收藏
页码:553 / 566
页数:14
相关论文
共 131 条
[1]   Advances in engineering local drug delivery systems for cancer immunotherapy [J].
Abdou, Peter ;
Wang, Zejun ;
Chen, Qian ;
Chan, Amanda ;
Zhou, Daojia R. ;
Gunadhi, Vivienne ;
Gu, Zhen .
WILEY INTERDISCIPLINARY REVIEWS-NANOMEDICINE AND NANOBIOTECHNOLOGY, 2020, 12 (05)
[2]   Nanomedicine and Onco-Immunotherapy: From the Bench to Bedside to Biomarkers [J].
Acebes-Fernandez, Vanessa ;
Landeira-Vinuela, Alicia ;
Juanes-Velasco, Pablo ;
Hernandez, Angela-Patricia ;
Otazo-Perez, Andrea ;
Manzano-Roman, Raul ;
Gongora, Rafael ;
Fuentes, Manuel .
NANOMATERIALS, 2020, 10 (07) :1-72
[3]   Nanoparticles and cancer therapy: Perspectives for application of nanoparticles in the treatment of cancers [J].
Aghebati-Maleki, Ali ;
Dolati, Sanam ;
Ahmadi, Majid ;
Baghbanzhadeh, Amir ;
Asadi, Milad ;
Fotouhi, Ali ;
Yousefi, Mehdi ;
Aghebati-Maleki, Leili .
JOURNAL OF CELLULAR PHYSIOLOGY, 2020, 235 (03) :1962-1972
[4]   Peptide-Drug Conjugates with Different Linkers for Cancer Therapy [J].
Alas, Mona ;
Saghaeidehkordi, Azam ;
Kaur, Kamaljit .
JOURNAL OF MEDICINAL CHEMISTRY, 2021, 64 (01) :216-232
[5]  
Anassi Enock, 2011, P T, V36, P197
[6]   Genome editing with CRISPR-Cas nucleases, base editors, transposases and prime editors [J].
Anzalone, Andrew V. ;
Koblan, Luke W. ;
Liu, David R. .
NATURE BIOTECHNOLOGY, 2020, 38 (07) :824-844
[7]  
Atlihan-Gundogdu E, 2020, J PHARM INVEST, V50, P349
[8]   Modeling the process of human tumorigenesis [J].
Balani, Sneha ;
Nguyen, Long V. ;
Eaves, Connie J. .
NATURE COMMUNICATIONS, 2017, 8
[9]   Coinhibitory Pathways in Immunotherapy for Cancer [J].
Baumeister, Susanne H. ;
Freeman, Gordon J. ;
Dranoff, Glenn ;
Sharpe, Arlene H. .
ANNUAL REVIEW OF IMMUNOLOGY, VOL 34, 2016, 34 :539-573
[10]   Advances in the development of personalized neoantigen-based therapeutic cancer vaccines [J].
Blass, Eryn ;
Ott, Patrick A. .
NATURE REVIEWS CLINICAL ONCOLOGY, 2021, 18 (04) :215-229