TNF‐derived peptides inhibit tumour growth and metastasis through cytolytic effects on tumour lymphatics

<p style="text-align:justify;"> TNF is a multifunctional cytokine with profound and diverse effects on physiology and pathology. Identifying the molecular determinants underlying the functions and pathogenic effects of TNF is key to understanding its mechanisms of action and identif...

Full description

Bibliographic Details
Main Authors: Lu, W, Wang, Y, Zhang, Q, Owen, S, Green, M, Ni, T, Edwards, M, Li, Y, Zhang, L, Harris, A, Li, J, Jackson, D, Jiang, S
Format: Journal article
Language:English
Published: Wiley 2019
_version_ 1826293189596676096
author Lu, W
Wang, Y
Zhang, Q
Owen, S
Green, M
Ni, T
Edwards, M
Li, Y
Zhang, L
Harris, A
Li, J
Jackson, D
Jiang, S
author_facet Lu, W
Wang, Y
Zhang, Q
Owen, S
Green, M
Ni, T
Edwards, M
Li, Y
Zhang, L
Harris, A
Li, J
Jackson, D
Jiang, S
author_sort Lu, W
collection OXFORD
description <p style="text-align:justify;"> TNF is a multifunctional cytokine with profound and diverse effects on physiology and pathology. Identifying the molecular determinants underlying the functions and pathogenic effects of TNF is key to understanding its mechanisms of action and identifying new therapeutic opportunities based on this important molecule. Previously, we showed that some evolutionarily‐conserved peptides derived from TNF could induce cell death (e.g. apoptosis and/or necrosis), a feature of immune defence mechanisms shared by many vertebrates. In this study, we demonstrated that necrosis‐inducing peptide P16 kills human glioblastoma cancer cells and primary human hepatoma or renal cancer cells isolated from patients who had not responded to standard treatments. Importantly we show that the necrosis‐inducing peptide P1516 significantly improves survival by inhibiting tumour metastasis in a 4T1 breast cancer syngeneic graft mouse model. As the lymphatic system is an important metastatic route in many cancers, we also tested the effect of TNF‐derived peptides on monolayers of primary human lymphatic endothelial cells (hDLEC) and found that they increased junctional permeability by inducing cytoskeletal reorganisation, gap junction formation and cell death. TEM imaging evidence, structural analysis and in vitro liposome leakage experiments strongly suggest that this killing is due to the cytolytic nature of these peptides. P1516 provides another example of a pro‐cytotoxic TNF peptide that likely functions as a cryptic necrotic factor released by TNF degradation. Its ability to inhibit tumour metastasis and improve survival may form the basis of a novel approach to cancer therapy.</p>
first_indexed 2024-03-07T03:26:16Z
format Journal article
id oxford-uuid:b9245601-afe7-41c5-a215-8cdcfa2019f2
institution University of Oxford
language English
last_indexed 2024-03-07T03:26:16Z
publishDate 2019
publisher Wiley
record_format dspace
spelling oxford-uuid:b9245601-afe7-41c5-a215-8cdcfa2019f22022-03-27T05:01:01ZTNF‐derived peptides inhibit tumour growth and metastasis through cytolytic effects on tumour lymphaticsJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:b9245601-afe7-41c5-a215-8cdcfa2019f2EnglishSymplectic Elements at OxfordWiley2019Lu, WWang, YZhang, QOwen, SGreen, MNi, TEdwards, MLi, YZhang, LHarris, ALi, JJackson, DJiang, S <p style="text-align:justify;"> TNF is a multifunctional cytokine with profound and diverse effects on physiology and pathology. Identifying the molecular determinants underlying the functions and pathogenic effects of TNF is key to understanding its mechanisms of action and identifying new therapeutic opportunities based on this important molecule. Previously, we showed that some evolutionarily‐conserved peptides derived from TNF could induce cell death (e.g. apoptosis and/or necrosis), a feature of immune defence mechanisms shared by many vertebrates. In this study, we demonstrated that necrosis‐inducing peptide P16 kills human glioblastoma cancer cells and primary human hepatoma or renal cancer cells isolated from patients who had not responded to standard treatments. Importantly we show that the necrosis‐inducing peptide P1516 significantly improves survival by inhibiting tumour metastasis in a 4T1 breast cancer syngeneic graft mouse model. As the lymphatic system is an important metastatic route in many cancers, we also tested the effect of TNF‐derived peptides on monolayers of primary human lymphatic endothelial cells (hDLEC) and found that they increased junctional permeability by inducing cytoskeletal reorganisation, gap junction formation and cell death. TEM imaging evidence, structural analysis and in vitro liposome leakage experiments strongly suggest that this killing is due to the cytolytic nature of these peptides. P1516 provides another example of a pro‐cytotoxic TNF peptide that likely functions as a cryptic necrotic factor released by TNF degradation. Its ability to inhibit tumour metastasis and improve survival may form the basis of a novel approach to cancer therapy.</p>
spellingShingle Lu, W
Wang, Y
Zhang, Q
Owen, S
Green, M
Ni, T
Edwards, M
Li, Y
Zhang, L
Harris, A
Li, J
Jackson, D
Jiang, S
TNF‐derived peptides inhibit tumour growth and metastasis through cytolytic effects on tumour lymphatics
title TNF‐derived peptides inhibit tumour growth and metastasis through cytolytic effects on tumour lymphatics
title_full TNF‐derived peptides inhibit tumour growth and metastasis through cytolytic effects on tumour lymphatics
title_fullStr TNF‐derived peptides inhibit tumour growth and metastasis through cytolytic effects on tumour lymphatics
title_full_unstemmed TNF‐derived peptides inhibit tumour growth and metastasis through cytolytic effects on tumour lymphatics
title_short TNF‐derived peptides inhibit tumour growth and metastasis through cytolytic effects on tumour lymphatics
title_sort tnf derived peptides inhibit tumour growth and metastasis through cytolytic effects on tumour lymphatics
work_keys_str_mv AT luw tnfderivedpeptidesinhibittumourgrowthandmetastasisthroughcytolyticeffectsontumourlymphatics
AT wangy tnfderivedpeptidesinhibittumourgrowthandmetastasisthroughcytolyticeffectsontumourlymphatics
AT zhangq tnfderivedpeptidesinhibittumourgrowthandmetastasisthroughcytolyticeffectsontumourlymphatics
AT owens tnfderivedpeptidesinhibittumourgrowthandmetastasisthroughcytolyticeffectsontumourlymphatics
AT greenm tnfderivedpeptidesinhibittumourgrowthandmetastasisthroughcytolyticeffectsontumourlymphatics
AT nit tnfderivedpeptidesinhibittumourgrowthandmetastasisthroughcytolyticeffectsontumourlymphatics
AT edwardsm tnfderivedpeptidesinhibittumourgrowthandmetastasisthroughcytolyticeffectsontumourlymphatics
AT liy tnfderivedpeptidesinhibittumourgrowthandmetastasisthroughcytolyticeffectsontumourlymphatics
AT zhangl tnfderivedpeptidesinhibittumourgrowthandmetastasisthroughcytolyticeffectsontumourlymphatics
AT harrisa tnfderivedpeptidesinhibittumourgrowthandmetastasisthroughcytolyticeffectsontumourlymphatics
AT lij tnfderivedpeptidesinhibittumourgrowthandmetastasisthroughcytolyticeffectsontumourlymphatics
AT jacksond tnfderivedpeptidesinhibittumourgrowthandmetastasisthroughcytolyticeffectsontumourlymphatics
AT jiangs tnfderivedpeptidesinhibittumourgrowthandmetastasisthroughcytolyticeffectsontumourlymphatics