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TRAIL in the Treatment of Cancer: From Soluble Cytokine to Nanosystems.

作者信息

Alizadeh Zeinabad Hojjat, Szegezdi Eva

机构信息

Apoptosis Research Centre, Biomedical Sciences Building, School of Biological and Chemical Sciences, University of Galway, H91 W2TY Galway, Ireland.

Science Foundation Ireland (SFI) Centre for Research in Medical Devices (CÚRAM), Biomedical Sciences Building, University of Galway, H91 W2TY Galway, Ireland.

出版信息

Cancers (Basel). 2022 Oct 19;14(20):5125. doi: 10.3390/cancers14205125.


DOI:10.3390/cancers14205125
PMID:36291908
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9600485/
Abstract

The death ligand tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL), a member of the TNF cytokine superfamily, has long been recognized for its potential as a cancer therapeutic due to its low toxicity against normal cells. However, its translation into a therapeutic molecule has not been successful to date, due to its short in vivo half-life associated with insufficient tumor accumulation and resistance of tumor cells to TRAIL-induced killing. Nanotechnology has the capacity to offer solutions to these limitations. This review provides a perspective and a critical assessment of the most promising approaches to realize TRAIL's potential as an anticancer therapeutic, including the development of fusion constructs, encapsulation, nanoparticle functionalization and tumor-targeting, and discusses the current challenges and future perspectives.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6470/9600485/3eb6d25fe6dd/cancers-14-05125-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6470/9600485/d4e9a7634d93/cancers-14-05125-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6470/9600485/c9cf73c2ab92/cancers-14-05125-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6470/9600485/3eb6d25fe6dd/cancers-14-05125-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6470/9600485/d4e9a7634d93/cancers-14-05125-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6470/9600485/c9cf73c2ab92/cancers-14-05125-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6470/9600485/3eb6d25fe6dd/cancers-14-05125-g003.jpg

相似文献

[1]
TRAIL in the Treatment of Cancer: From Soluble Cytokine to Nanosystems.

Cancers (Basel). 2022-10-19

[2]
Nano-TRAIL: a promising path to cancer therapy.

Cancer Drug Resist. 2023-2-1

[3]
Tumor necrosis factor-related apoptosis-inducing ligand-mediated apoptosis in established and primary glioma cell lines.

Neurosurg Focus. 2002-9-15

[4]
TRAILblazing Strategies for Cancer Treatment.

Cancers (Basel). 2019-3-30

[5]
The Role of TRAIL Signaling in Cancer: Searching for New Therapeutic Strategies.

Biology (Basel). 2024-7-15

[6]
Traditional Chinese medicines and their active ingredients sensitize cancer cells to TRAIL-induced apoptosis.

J Zhejiang Univ Sci B. 2021-3-15

[7]
Down-regulation of protein kinase Ceta potentiates the cytotoxic effects of exogenous tumor necrosis factor-related apoptosis-inducing ligand in PC-3 prostate cancer cells.

Mol Cancer Ther. 2004-7

[8]
Fn14•TRAIL effectively inhibits hepatocellular carcinoma growth.

PLoS One. 2013-10-10

[9]
Fused hydrophobic elastin-like-peptides (ELP) enhance biological activity of tumor necrosis factor-related apoptosis-inducing ligand (TRAIL).

Protein Pept Lett. 2015

[10]
Interactions of Tumor Necrosis Factor-Related Apoptosis-Inducing Ligand (TRAIL) with the Immune System: Implications for Inflammation and Cancer.

Cancers (Basel). 2019-8-13

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World J Clin Oncol. 2025-8-24

[2]
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[3]
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Biomater Res. 2025-6-10

[4]
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[5]
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[6]
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Transl Androl Urol. 2024-7-31

[7]
The Multifaceted Functionality of Plasmacytoid Dendritic Cells in Gastrointestinal Cancers: A Potential Therapeutic Target?

Cancers (Basel). 2024-6-13

[8]
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[9]
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Sci Rep. 2024-2-6

[10]
An Antidepressant Drug Increased TRAIL Receptor-2 Expression and Sensitized Lung Cancer Cells to TRAIL-induced Apoptosis.

Anticancer Agents Med Chem. 2023

本文引用的文献

[1]
TRAIL-modified, doxorubicin-embedded periodic mesoporous organosilica nanoparticles for targeted drug delivery and efficient antitumor immunotherapy.

Acta Biomater. 2022-4-15

[2]
Distinct binding kinetics of E-, P- and L-selectins to CD44.

FEBS J. 2022-5

[3]
An engineered construct of cFLIP provides insight into DED1 structure and interactions.

Structure. 2022-2-3

[4]
Extracellular vesicles in pancreatic cancer progression and therapies.

Cell Death Dis. 2021-10-20

[5]
Recent Strategies to Develop Innovative Photosensitizers for Enhanced Photodynamic Therapy.

Chem Rev. 2021-11-10

[6]
Diagnostic and drug release systems based on microneedle arrays in breast cancer therapy.

J Control Release. 2021-10-10

[7]
TRAIL-overexpressing Adipose Tissue-derived Mesenchymal Stem Cells Efficiently Inhibit Tumor Growth in an H460 Xenograft Model.

Cancer Genomics Proteomics. 2021

[8]
Recent progress in targeted delivery vectors based on biomimetic nanoparticles.

Signal Transduct Target Ther. 2021-6-7

[9]
Recent advances in cell membrane coated metal-organic frameworks (MOFs) for tumor therapy.

J Mater Chem B. 2021-6-2

[10]
Splicing reprogramming of TRAIL/DISC-components sensitizes lung cancer cells to TRAIL-mediated apoptosis.

Cell Death Dis. 2021-3-17

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