Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Qin, Xiaodong, Du, Yuping, Chen, Xing, Li, Wuyan, Zhang, Jinghong, Yang, Jinbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
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
_version_ 1782327703510188032
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
work_keys_str_mv AT qinxiaodong activationofaktprotectscancercellsfromgrowthinhibitioninducedbypkm2knockdown
AT duyuping activationofaktprotectscancercellsfromgrowthinhibitioninducedbypkm2knockdown
AT chenxing activationofaktprotectscancercellsfromgrowthinhibitioninducedbypkm2knockdown
AT liwuyan activationofaktprotectscancercellsfromgrowthinhibitioninducedbypkm2knockdown
AT zhangjinghong activationofaktprotectscancercellsfromgrowthinhibitioninducedbypkm2knockdown
AT yangjinbo activationofaktprotectscancercellsfromgrowthinhibitioninducedbypkm2knockdown