Literature DB >> 24387131

The significance of transferrin receptors in oncology: the development of functional nano-based drug delivery systems.

Stephanie Tortorella, Tom C Karagiannis1.   

Abstract

Anticancer therapeutic research aims to improve clinical management of the disease through the development of strategies that involve currently-relevant treatment options and targeted delivery. Tumour-specific and -targeted delivery of compounds to the site of malignancy allows for enhanced cellular uptake, increased therapeutic benefit with high intratumoural drug concentrations, and decreased systemic exposure. Due to the upregulation of transferrin receptor expression in a wide variety of cancers, its function and its highly efficient recycling pathway, strategies involving the selective targeting of the receptor are well documented. Direct conjugation and immunotoxin studies using the transferrin peptide or anti-transferrin receptor antibodies as the targeting moiety have established the capacity to enhance cellular uptake, cross the blood brain barrier, limit systemic toxicity and reverse multi-drug resistance. Limitations in direct conjugation, including the difficulty in linking an adequate amount of therapeutic compound to the ligand or antibody have identified the requirement to develop novel delivery methods. The application of nanoparticulate theory in the development of functional drug delivery systems has proven to be most promising, with the ability to selectively modify size-dependent properties and surface chemistry. The transferrin modification on a range of nanoparticle formulations enhances selective cellular uptake through transferrin-mediated processes, and increases therapeutic benefit through the ability to encapsulate high concentrations of relevant drug to the tumour site. Although ineffective in crossing the blood brain barrier in its free form, chemotherapeutic compounds including doxorubicin, may be loaded into transferrin-conjugated nanocarriers and impart cytotoxic effects in glioma cells in vitro and in vivo. Additionally, transferrin-targeted nanoparticles may be used in selective diagnostic applications with enhanced selectivity and sensitivity. Four transferrin-modified nano-based drug delivery systems are currently in early phases of human clinical trials. Despite the collective promise, inconsistencies in some studies have exposed some limitations in current formulations and the difficulty in translating preliminary studies into clinically-relevant therapeutic options. The main objective of this review is to investigate the development of transferrin targeted nano-based drug delivery systems in order to establish the use of transferrin as a cancer-targeted moiety, and to ultimately evaluate the progression of cancer therapeutic strategies for future research.

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Year:  2014        PMID: 24387131     DOI: 10.2174/1567201810666140106115436

Source DB:  PubMed          Journal:  Curr Drug Deliv        ISSN: 1567-2018            Impact factor:   2.565


  14 in total

1.  A critical evaluation of drug delivery from ligand modified nanoparticles: Confounding small molecule distribution and efficacy in the central nervous system.

Authors:  Rebecca L Cook; Kyle T Householder; Eugene P Chung; Alesia V Prakapenka; Danielle M DiPerna; Rachael W Sirianni
Journal:  J Control Release       Date:  2015-10-22       Impact factor: 9.776

Review 2.  Crossing the barrier: treatment of brain tumors using nanochain particles.

Authors:  Efstathios Karathanasis; Ketan B Ghaghada
Journal:  Wiley Interdiscip Rev Nanomed Nanobiotechnol       Date:  2016-01-09

3.  Transferrin Receptor Targeted Cellular Delivery of Doxorubicin Via a Reduction-Responsive Peptide-Drug Conjugate.

Authors:  Songtao Li; Hongling Zhao; Xiaoxia Mao; Yanfang Fan; Xiujun Liang; Ruxing Wang; Lijun Xiao; Jianping Wang; Qi Liu; Guiqin Zhao
Journal:  Pharm Res       Date:  2019-10-25       Impact factor: 4.200

4.  Albumin-assisted exfoliated ultrathin rhenium disulfide nanosheets as a tumor targeting and dual-stimuli-responsive drug delivery system for a combination chemo-photothermal treatment.

Authors:  Qunlian Huang; Shurong Wang; Jie Zhou; Xiaoyan Zhong; Yilan Huang
Journal:  RSC Adv       Date:  2018-01-25       Impact factor: 4.036

5.  Plasmid pORF-hTRAIL targeting to glioma using transferrin-modified polyamidoamine dendrimer.

Authors:  Song Gao; Jianfeng Li; Chen Jiang; Bo Hong; Bing Hao
Journal:  Drug Des Devel Ther       Date:  2015-12-17       Impact factor: 4.162

6.  PLGA-PLL-PEG-Tf-based targeted nanoparticles drug delivery system enhance antitumor efficacy via intrinsic apoptosis pathway.

Authors:  Wen Bao; Ran Liu; Yonglu Wang; Fei Wang; Guohua Xia; Haijun Zhang; Xueming Li; Haixiang Yin; Baoan Chen
Journal:  Int J Nanomedicine       Date:  2015-01-12

7.  Global view of a drug-sensitivity gene network.

Authors:  Haixiu Yang; Yunpeng Zhang; Jiasheng Wang; Tan Wu; Siyao Liu; Yanjun Xu; Desi Shang
Journal:  Oncotarget       Date:  2017-12-14

Review 8.  Glioma: experimental models and reality.

Authors:  Krissie Lenting; Roel Verhaak; Mark Ter Laan; Pieter Wesseling; William Leenders
Journal:  Acta Neuropathol       Date:  2017-01-10       Impact factor: 17.088

9.  Fabrication and evaluation of a γ-PGA-based self-assembly transferrin receptor-targeting anticancer drug carrier.

Authors:  Li Zhang; Xiaoyu Zhu; Shijia Wu; Yazhou Chen; Shiming Tan; Yingjie Liu; Wenzheng Jiang; Jing Huang
Journal:  Int J Nanomedicine       Date:  2018-11-22

10.  Blood-brain barrier amenable gold nanoparticles biofabrication in aged cell culture medium.

Authors:  F U Rehman; J Bao; P Muhammad; W He; S Hanif; M A Rauf
Journal:  Mater Today Bio       Date:  2020-08-07
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