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Activation of Akt protects cancer cells from growth inhibition induced by PKM2 knockdown
BACKGROUND: PKM2 is an attractive target for cancer therapy, however, for many cancer cells, PKM2 knockdown only leads to a modest impairment of survival and proliferation. It is not known whether PKM2 knockdown rewires cell signaling pathways in these “PKM2 knockdown resistant” cells, and whether t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4108064/ https://www.ncbi.nlm.nih.gov/pubmed/24735734 http://dx.doi.org/10.1186/2045-3701-4-20 |
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author | Qin, Xiaodong Du, Yuping Chen, Xing Li, Wuyan Zhang, Jinghong Yang, Jinbo |
author_facet | Qin, Xiaodong Du, Yuping Chen, Xing Li, Wuyan Zhang, Jinghong Yang, Jinbo |
author_sort | Qin, Xiaodong |
collection | PubMed |
description | BACKGROUND: PKM2 is an attractive target for cancer therapy, however, for many cancer cells, PKM2 knockdown only leads to a modest impairment of survival and proliferation. It is not known whether PKM2 knockdown rewires cell signaling pathways in these “PKM2 knockdown resistant” cells, and whether the rewired pathways are needed for their survival. FINDINGS: In present study, we investigated the effects of PKM2 knockdown on cellular signaling pathways in “PKM2 knockdown resistant” cancer cells. We found that knockdown of PKM2 leads to activation of Akt. Furthermore, we revealed that activation of Akt in PKM2 knockdown cells is a result of glycolysis disruption. Inhibiton of PI3K-Akt signaling pathway leads to significant growth inhibition and apoptosis in PKM2 knockdown cells. CONCLUSIONS: Overall, our results indicate that activation of Akt is necessary for the survival of PKM2 knockdown cells. Combing PKM2 knockdown with PI3K or Akt inhibitors may lead to a better chance to kill tumors. Our research may provide an unexpected opportunity for the development and implementation of drugs targeting cell metabolism and aberrant Akt signaling. |
format | Online Article Text |
id | pubmed-4108064 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41080642014-07-24 Activation of Akt protects cancer cells from growth inhibition induced by PKM2 knockdown Qin, Xiaodong Du, Yuping Chen, Xing Li, Wuyan Zhang, Jinghong Yang, Jinbo Cell Biosci Short Report BACKGROUND: PKM2 is an attractive target for cancer therapy, however, for many cancer cells, PKM2 knockdown only leads to a modest impairment of survival and proliferation. It is not known whether PKM2 knockdown rewires cell signaling pathways in these “PKM2 knockdown resistant” cells, and whether the rewired pathways are needed for their survival. FINDINGS: In present study, we investigated the effects of PKM2 knockdown on cellular signaling pathways in “PKM2 knockdown resistant” cancer cells. We found that knockdown of PKM2 leads to activation of Akt. Furthermore, we revealed that activation of Akt in PKM2 knockdown cells is a result of glycolysis disruption. Inhibiton of PI3K-Akt signaling pathway leads to significant growth inhibition and apoptosis in PKM2 knockdown cells. CONCLUSIONS: Overall, our results indicate that activation of Akt is necessary for the survival of PKM2 knockdown cells. Combing PKM2 knockdown with PI3K or Akt inhibitors may lead to a better chance to kill tumors. Our research may provide an unexpected opportunity for the development and implementation of drugs targeting cell metabolism and aberrant Akt signaling. BioMed Central 2014-04-15 /pmc/articles/PMC4108064/ /pubmed/24735734 http://dx.doi.org/10.1186/2045-3701-4-20 Text en Copyright © 2014 Qin et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 | Short Report Qin, Xiaodong Du, Yuping Chen, Xing Li, Wuyan Zhang, Jinghong Yang, Jinbo Activation of Akt protects cancer cells from growth inhibition induced by PKM2 knockdown |
title | Activation of Akt protects cancer cells from growth inhibition induced by PKM2 knockdown |
title_full | Activation of Akt protects cancer cells from growth inhibition induced by PKM2 knockdown |
title_fullStr | Activation of Akt protects cancer cells from growth inhibition induced by PKM2 knockdown |
title_full_unstemmed | Activation of Akt protects cancer cells from growth inhibition induced by PKM2 knockdown |
title_short | Activation of Akt protects cancer cells from growth inhibition induced by PKM2 knockdown |
title_sort | activation of akt protects cancer cells from growth inhibition induced by pkm2 knockdown |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4108064/ https://www.ncbi.nlm.nih.gov/pubmed/24735734 http://dx.doi.org/10.1186/2045-3701-4-20 |
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