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Anti-tumor activities and apoptotic mechanism of ribosome-inactivating proteins
Ribosome-inactivating proteins (RIPs) belong to a family of enzymes that attack eukaryotic ribosomes and potently inhibit cellular protein synthesis. RIPs possess several biomedical properties, including anti-viral and anti-tumor activities. Multiple RIPs are known to inhibit tumor cell proliferatio...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4593346/ https://www.ncbi.nlm.nih.gov/pubmed/26184404 http://dx.doi.org/10.1186/s40880-015-0030-x |
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author | Zeng, Meiqi Zheng, Manyin Lu, Desheng Wang, Jun Jiang, Wenqi Sha, Ou |
author_facet | Zeng, Meiqi Zheng, Manyin Lu, Desheng Wang, Jun Jiang, Wenqi Sha, Ou |
author_sort | Zeng, Meiqi |
collection | PubMed |
description | Ribosome-inactivating proteins (RIPs) belong to a family of enzymes that attack eukaryotic ribosomes and potently inhibit cellular protein synthesis. RIPs possess several biomedical properties, including anti-viral and anti-tumor activities. Multiple RIPs are known to inhibit tumor cell proliferation through inducing apoptosis in a variety of cancers, such as breast cancer, leukemia/lymphoma, and hepatoma. This review focuses on the anti-tumor activities of RIPs and their apoptotic effects through three closely related pathways: mitochondrial, death receptor, and endoplasmic reticulum pathways. |
format | Online Article Text |
id | pubmed-4593346 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45933462015-10-06 Anti-tumor activities and apoptotic mechanism of ribosome-inactivating proteins Zeng, Meiqi Zheng, Manyin Lu, Desheng Wang, Jun Jiang, Wenqi Sha, Ou Chin J Cancer Review Ribosome-inactivating proteins (RIPs) belong to a family of enzymes that attack eukaryotic ribosomes and potently inhibit cellular protein synthesis. RIPs possess several biomedical properties, including anti-viral and anti-tumor activities. Multiple RIPs are known to inhibit tumor cell proliferation through inducing apoptosis in a variety of cancers, such as breast cancer, leukemia/lymphoma, and hepatoma. This review focuses on the anti-tumor activities of RIPs and their apoptotic effects through three closely related pathways: mitochondrial, death receptor, and endoplasmic reticulum pathways. BioMed Central 2015-07-17 /pmc/articles/PMC4593346/ /pubmed/26184404 http://dx.doi.org/10.1186/s40880-015-0030-x Text en © Zeng et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Zeng, Meiqi Zheng, Manyin Lu, Desheng Wang, Jun Jiang, Wenqi Sha, Ou Anti-tumor activities and apoptotic mechanism of ribosome-inactivating proteins |
title | Anti-tumor activities and apoptotic mechanism of ribosome-inactivating proteins |
title_full | Anti-tumor activities and apoptotic mechanism of ribosome-inactivating proteins |
title_fullStr | Anti-tumor activities and apoptotic mechanism of ribosome-inactivating proteins |
title_full_unstemmed | Anti-tumor activities and apoptotic mechanism of ribosome-inactivating proteins |
title_short | Anti-tumor activities and apoptotic mechanism of ribosome-inactivating proteins |
title_sort | anti-tumor activities and apoptotic mechanism of ribosome-inactivating proteins |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4593346/ https://www.ncbi.nlm.nih.gov/pubmed/26184404 http://dx.doi.org/10.1186/s40880-015-0030-x |
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