AMP-activated protein kinase regulates the expression of human telomerase reverse transcriptase.

The expression of hTERT in tumor cells contributes to oncogenic transformation by promoting immortalization. For this reason, hTERT is one of the major targets for cancer therapy, and an efficient method to downregulate hTERT expression is required for treatment of hTERT-positive cancer. In this rep...

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Main Authors: Daum Jo, Rackhyun Park, Hyunju Kim, Minsu Jang, Eun-Ju Lee, Ik-Soon Jang, Junsoo Park
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC6257937?pdf=render
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spelling doaj-67cba7610a4f43a584eeb6ea0bc491782020-11-24T22:18:40ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-011311e020786410.1371/journal.pone.0207864AMP-activated protein kinase regulates the expression of human telomerase reverse transcriptase.Daum JoRackhyun ParkHyunju KimMinsu JangEun-Ju LeeIk-Soon JangJunsoo ParkThe expression of hTERT in tumor cells contributes to oncogenic transformation by promoting immortalization. For this reason, hTERT is one of the major targets for cancer therapy, and an efficient method to downregulate hTERT expression is required for treatment of hTERT-positive cancer. In this report, we demonstrated that inhibition of AMP-activated protein kinase (AMPK) downregulates the expression of hTERT. We screened cell signaling pathways in AMPK α1 knockout cells and found that AMPKα1 is required for activity of the hTERT promoter. AMPKα1 knockout cells showed decreased expression of hTERT mRNA and protein. We also demonstrated that compound C, a reversible AMPK inhibitor, suppressed the expression of hTERT. However, AMPK activators, including AICAR and metformin, did not increase the level of hTERT protein. Finally, we showed that tumor cells stably expressing hTERT are resistant to compound C treatment. These results indicate that AMPK activity is required for tumor progression.http://europepmc.org/articles/PMC6257937?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Daum Jo
Rackhyun Park
Hyunju Kim
Minsu Jang
Eun-Ju Lee
Ik-Soon Jang
Junsoo Park
spellingShingle Daum Jo
Rackhyun Park
Hyunju Kim
Minsu Jang
Eun-Ju Lee
Ik-Soon Jang
Junsoo Park
AMP-activated protein kinase regulates the expression of human telomerase reverse transcriptase.
PLoS ONE
author_facet Daum Jo
Rackhyun Park
Hyunju Kim
Minsu Jang
Eun-Ju Lee
Ik-Soon Jang
Junsoo Park
author_sort Daum Jo
title AMP-activated protein kinase regulates the expression of human telomerase reverse transcriptase.
title_short AMP-activated protein kinase regulates the expression of human telomerase reverse transcriptase.
title_full AMP-activated protein kinase regulates the expression of human telomerase reverse transcriptase.
title_fullStr AMP-activated protein kinase regulates the expression of human telomerase reverse transcriptase.
title_full_unstemmed AMP-activated protein kinase regulates the expression of human telomerase reverse transcriptase.
title_sort amp-activated protein kinase regulates the expression of human telomerase reverse transcriptase.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2018-01-01
description The expression of hTERT in tumor cells contributes to oncogenic transformation by promoting immortalization. For this reason, hTERT is one of the major targets for cancer therapy, and an efficient method to downregulate hTERT expression is required for treatment of hTERT-positive cancer. In this report, we demonstrated that inhibition of AMP-activated protein kinase (AMPK) downregulates the expression of hTERT. We screened cell signaling pathways in AMPK α1 knockout cells and found that AMPKα1 is required for activity of the hTERT promoter. AMPKα1 knockout cells showed decreased expression of hTERT mRNA and protein. We also demonstrated that compound C, a reversible AMPK inhibitor, suppressed the expression of hTERT. However, AMPK activators, including AICAR and metformin, did not increase the level of hTERT protein. Finally, we showed that tumor cells stably expressing hTERT are resistant to compound C treatment. These results indicate that AMPK activity is required for tumor progression.
url http://europepmc.org/articles/PMC6257937?pdf=render
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