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Apoptotic Sphingolipid Ceramide in Cancer Therapy
Apoptosis, also called programmed cell death, is physiologically and pathologically involved in cellular homeostasis. Escape of apoptotic signaling is a critical strategy commonly used for cancer tumorigenesis. Ceramide, a derivative of sphingolipid breakdown products, acts as second messenger for m...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3066853/ https://www.ncbi.nlm.nih.gov/pubmed/21490804 http://dx.doi.org/10.1155/2011/565316 |
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author | Huang, Wei-Ching Chen, Chia-Ling Lin, Yee-Shin Lin, Chiou-Feng |
author_facet | Huang, Wei-Ching Chen, Chia-Ling Lin, Yee-Shin Lin, Chiou-Feng |
author_sort | Huang, Wei-Ching |
collection | PubMed |
description | Apoptosis, also called programmed cell death, is physiologically and pathologically involved in cellular homeostasis. Escape of apoptotic signaling is a critical strategy commonly used for cancer tumorigenesis. Ceramide, a derivative of sphingolipid breakdown products, acts as second messenger for multiple extracellular stimuli including growth factors, chemical agents, and environmental stresses, such as hypoxia, and heat stress as well as irradiation. Also, ceramide acts as tumor-suppressor lipid because a variety of stress stimuli cause apoptosis by increasing intracellular ceramide to initiate apoptotic signaling. Defects on ceramide generation and sphingolipid metabolism are developed for cancer cell survival and cancer therapy resistance. Alternatively, targeting ceramide metabolism to correct these defects might provide opportunities to overcome cancer therapy resistance. |
format | Text |
id | pubmed-3066853 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-30668532011-04-13 Apoptotic Sphingolipid Ceramide in Cancer Therapy Huang, Wei-Ching Chen, Chia-Ling Lin, Yee-Shin Lin, Chiou-Feng J Lipids Review Article Apoptosis, also called programmed cell death, is physiologically and pathologically involved in cellular homeostasis. Escape of apoptotic signaling is a critical strategy commonly used for cancer tumorigenesis. Ceramide, a derivative of sphingolipid breakdown products, acts as second messenger for multiple extracellular stimuli including growth factors, chemical agents, and environmental stresses, such as hypoxia, and heat stress as well as irradiation. Also, ceramide acts as tumor-suppressor lipid because a variety of stress stimuli cause apoptosis by increasing intracellular ceramide to initiate apoptotic signaling. Defects on ceramide generation and sphingolipid metabolism are developed for cancer cell survival and cancer therapy resistance. Alternatively, targeting ceramide metabolism to correct these defects might provide opportunities to overcome cancer therapy resistance. Hindawi Publishing Corporation 2011 2011-01-13 /pmc/articles/PMC3066853/ /pubmed/21490804 http://dx.doi.org/10.1155/2011/565316 Text en Copyright © 2011 Wei-Ching Huang et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Huang, Wei-Ching Chen, Chia-Ling Lin, Yee-Shin Lin, Chiou-Feng Apoptotic Sphingolipid Ceramide in Cancer Therapy |
title | Apoptotic Sphingolipid Ceramide in Cancer Therapy |
title_full | Apoptotic Sphingolipid Ceramide in Cancer Therapy |
title_fullStr | Apoptotic Sphingolipid Ceramide in Cancer Therapy |
title_full_unstemmed | Apoptotic Sphingolipid Ceramide in Cancer Therapy |
title_short | Apoptotic Sphingolipid Ceramide in Cancer Therapy |
title_sort | apoptotic sphingolipid ceramide in cancer therapy |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3066853/ https://www.ncbi.nlm.nih.gov/pubmed/21490804 http://dx.doi.org/10.1155/2011/565316 |
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