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Survivin as a Preferential Target for Cancer Therapy
Cancer is typically a consequence of imbalance between cell death and proliferation in a way favorable to cell proliferation and survival. Most conventional cancer therapies are based on targeting rapidly growing cancerous cells to block growth or enhance cell death, thereby, restoring the balance b...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3958864/ https://www.ncbi.nlm.nih.gov/pubmed/24531137 http://dx.doi.org/10.3390/ijms15022494 |
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author | Mobahat, Mahsa Narendran, Aru Riabowol, Karl |
author_facet | Mobahat, Mahsa Narendran, Aru Riabowol, Karl |
author_sort | Mobahat, Mahsa |
collection | PubMed |
description | Cancer is typically a consequence of imbalance between cell death and proliferation in a way favorable to cell proliferation and survival. Most conventional cancer therapies are based on targeting rapidly growing cancerous cells to block growth or enhance cell death, thereby, restoring the balance between these processes. In many instances, malignancies that develop resistance to current treatment modalities, such as chemotherapy, immunotherapy, and radiotherapy often present the greatest challenge in subsequent management of the patient. Studies have shown that under normal circumstances, cells utilize different death mechanisms, such as apoptosis (programmed cell death), autophagy, mitotic catastrophe, and necrosis to maintain homeostasis and physiological integrity of the organism, but these processes often appear to be altered in cancer. Thus, in recent years developing various strategies for administration of cytotoxic chemotherapeutics in combination with apoptosis-sensitizing reagents is receiving more emphasis. Here, we review the properties of the anti-apoptotic protein, survivin, a member of the inhibitor of apoptosis protein (IAP) family and the clinical feasibility and anti-cancer potential of drugs targeting this protein. We also discuss some key points and concerns that should be taken into consideration while developing drugs that target apoptotic proteins, such as survivin. |
format | Online Article Text |
id | pubmed-3958864 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-39588642014-03-20 Survivin as a Preferential Target for Cancer Therapy Mobahat, Mahsa Narendran, Aru Riabowol, Karl Int J Mol Sci Review Cancer is typically a consequence of imbalance between cell death and proliferation in a way favorable to cell proliferation and survival. Most conventional cancer therapies are based on targeting rapidly growing cancerous cells to block growth or enhance cell death, thereby, restoring the balance between these processes. In many instances, malignancies that develop resistance to current treatment modalities, such as chemotherapy, immunotherapy, and radiotherapy often present the greatest challenge in subsequent management of the patient. Studies have shown that under normal circumstances, cells utilize different death mechanisms, such as apoptosis (programmed cell death), autophagy, mitotic catastrophe, and necrosis to maintain homeostasis and physiological integrity of the organism, but these processes often appear to be altered in cancer. Thus, in recent years developing various strategies for administration of cytotoxic chemotherapeutics in combination with apoptosis-sensitizing reagents is receiving more emphasis. Here, we review the properties of the anti-apoptotic protein, survivin, a member of the inhibitor of apoptosis protein (IAP) family and the clinical feasibility and anti-cancer potential of drugs targeting this protein. We also discuss some key points and concerns that should be taken into consideration while developing drugs that target apoptotic proteins, such as survivin. Molecular Diversity Preservation International (MDPI) 2014-02-13 /pmc/articles/PMC3958864/ /pubmed/24531137 http://dx.doi.org/10.3390/ijms15022494 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Mobahat, Mahsa Narendran, Aru Riabowol, Karl Survivin as a Preferential Target for Cancer Therapy |
title | Survivin as a Preferential Target for Cancer Therapy |
title_full | Survivin as a Preferential Target for Cancer Therapy |
title_fullStr | Survivin as a Preferential Target for Cancer Therapy |
title_full_unstemmed | Survivin as a Preferential Target for Cancer Therapy |
title_short | Survivin as a Preferential Target for Cancer Therapy |
title_sort | survivin as a preferential target for cancer therapy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3958864/ https://www.ncbi.nlm.nih.gov/pubmed/24531137 http://dx.doi.org/10.3390/ijms15022494 |
work_keys_str_mv | AT mobahatmahsa survivinasapreferentialtargetforcancertherapy AT narendranaru survivinasapreferentialtargetforcancertherapy AT riabowolkarl survivinasapreferentialtargetforcancertherapy |