TNF-derived peptides inhibit tumour growth and metastasis through cytolytic effects on tumour lymphatics
Autor: | Lina Zhang, Mark H. Edwards, Yuming Li, Qing Zhang, Sophie I Owen, Tao Ni, Adrian L. Harris, Shisong Jiang, Ying-Jie Wang, Lu Wenshu, Ji-Liang Li, David A. Jackson, Marcus Green |
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Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
Programmed cell death Necrosis medicine.medical_treatment Immunology Biology Metastasis Jurkat Cells 03 medical and health sciences 0302 clinical medicine Neoplasms Human Umbilical Vein Endothelial Cells medicine Humans Immunology and Allergy Neoplasm Metastasis Cytotoxins Tumor Necrosis Factor-alpha Endothelial Cells Original Articles medicine.disease 030104 developmental biology Lymphatic system Cytokine Apoptosis Cancer cell Cancer research Tumor necrosis factor alpha medicine.symptom Peptides 030215 immunology |
Zdroj: | Clin Exp Immunol |
ISSN: | 1365-2249 0009-9104 |
Popis: | Summary Tumour necrosis factor (TNF) is a multi-functional 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. Because 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 reorganization, gap junction formation and cell death. Transmission electron microscopy 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 probably 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. |
Databáze: | OpenAIRE |
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