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Death Receptors: New Opportunities in Cancer Therapy.
This article offers a detailed review of the current approaches to anticancer therapy that target the death receptors of malignant cells. Here, we provide a comprehensive overview of the structure and function of death receptors and their ligands, describe the current and latest trends in the develo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
A.I. Gordeyev
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662274/ https://www.ncbi.nlm.nih.gov/pubmed/29104776 |
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author | Ukrainskaya, V.M. Stepanov, A.V. Glagoleva, I.S. Knorre, V.D. Belogurov, A.A. Jr. Gabibov, A.G. |
author_facet | Ukrainskaya, V.M. Stepanov, A.V. Glagoleva, I.S. Knorre, V.D. Belogurov, A.A. Jr. Gabibov, A.G. |
author_sort | Ukrainskaya, V.M. |
collection | PubMed |
description | This article offers a detailed review of the current approaches to anticancer therapy that target the death receptors of malignant cells. Here, we provide a comprehensive overview of the structure and function of death receptors and their ligands, describe the current and latest trends in the development of death receptor agonists, and perform their comparative analysis. In addition, we discuss the DR4 and DR5 agonistic antibodies that are being evaluated at various stages of clinical trials. Finally, we conclude by stating that death receptor agonists may be improved through increasing their stability, solubility, and elimination half-life, as well as by overcoming the resistance of tumor cells. What’s more, effective application of these antibodies requires a more detailed study of their use in combination with other anticancer agents. |
format | Online Article Text |
id | pubmed-5662274 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | A.I. Gordeyev |
record_format | MEDLINE/PubMed |
spelling | pubmed-56622742017-11-03 Death Receptors: New Opportunities in Cancer Therapy. Ukrainskaya, V.M. Stepanov, A.V. Glagoleva, I.S. Knorre, V.D. Belogurov, A.A. Jr. Gabibov, A.G. Acta Naturae Research Article This article offers a detailed review of the current approaches to anticancer therapy that target the death receptors of malignant cells. Here, we provide a comprehensive overview of the structure and function of death receptors and their ligands, describe the current and latest trends in the development of death receptor agonists, and perform their comparative analysis. In addition, we discuss the DR4 and DR5 agonistic antibodies that are being evaluated at various stages of clinical trials. Finally, we conclude by stating that death receptor agonists may be improved through increasing their stability, solubility, and elimination half-life, as well as by overcoming the resistance of tumor cells. What’s more, effective application of these antibodies requires a more detailed study of their use in combination with other anticancer agents. A.I. Gordeyev 2017 /pmc/articles/PMC5662274/ /pubmed/29104776 Text en Copyright ® 2017 Park-media Ltd. http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Ukrainskaya, V.M. Stepanov, A.V. Glagoleva, I.S. Knorre, V.D. Belogurov, A.A. Jr. Gabibov, A.G. Death Receptors: New Opportunities in Cancer Therapy. |
title | Death Receptors: New Opportunities in Cancer Therapy. |
title_full | Death Receptors: New Opportunities in Cancer Therapy. |
title_fullStr | Death Receptors: New Opportunities in Cancer Therapy. |
title_full_unstemmed | Death Receptors: New Opportunities in Cancer Therapy. |
title_short | Death Receptors: New Opportunities in Cancer Therapy. |
title_sort | death receptors: new opportunities in cancer therapy. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662274/ https://www.ncbi.nlm.nih.gov/pubmed/29104776 |
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