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Lactate Dehydrogenase B Is Required for Pancreatic Cancer Cell Immortalization Through Activation of Telomerase Activity

Telomerase activity is elevated in most cancer cells and is required for telomere length maintenance and immortalization of cancer cells. Glucose metabolic reprogramming is a hallmark of cancer and accompanied with increased expression of key metabolic enzymes. Whether these enzymes influence telome...

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Autores principales: Wang, Ruiguan, Li, Jiangbo, Zhang, Changjian, Guan, Xin, Qin, Boyu, Jin, Rui, Qin, Lingmei, Xu, Shanrong, Zhang, Xiaona, Liu, Rong, Ye, Qinong, Cheng, Long
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9163669/
https://www.ncbi.nlm.nih.gov/pubmed/35669414
http://dx.doi.org/10.3389/fonc.2022.821620
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author Wang, Ruiguan
Li, Jiangbo
Zhang, Changjian
Guan, Xin
Qin, Boyu
Jin, Rui
Qin, Lingmei
Xu, Shanrong
Zhang, Xiaona
Liu, Rong
Ye, Qinong
Cheng, Long
author_facet Wang, Ruiguan
Li, Jiangbo
Zhang, Changjian
Guan, Xin
Qin, Boyu
Jin, Rui
Qin, Lingmei
Xu, Shanrong
Zhang, Xiaona
Liu, Rong
Ye, Qinong
Cheng, Long
author_sort Wang, Ruiguan
collection PubMed
description Telomerase activity is elevated in most cancer cells and is required for telomere length maintenance and immortalization of cancer cells. Glucose metabolic reprogramming is a hallmark of cancer and accompanied with increased expression of key metabolic enzymes. Whether these enzymes influence telomerase activity and cell immortalization remains unclear. In the current study, we screened metabolic enzymes using telomerase activity assay and identified lactate dehydrogenase B (LDHB) as a regulator of telomerase activity. Sodium lactate and sodium pyruvate did not influence telomerase activity, indicating LDHB regulates telomerase activity independent of its metabolism regulating function. Further studies revealed that LDHB directly interacted with TERT and regulated the interaction between TERT and TERC. Additionally, long-term knockdown of LDHB inhibited cancer cell growth and induced cell senescence in vitro and in vivo. Higher LDHB expression was detected in pancreatic cancer tissues compared with that in adjacent normal tissues and expression of LDHB correlated negatively with prognosis. Thus, we identified LDHB as the first glucose metabolic enzyme contributing to telomerase activity and pancreatic cancer cell immortalization.
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spelling pubmed-91636692022-06-05 Lactate Dehydrogenase B Is Required for Pancreatic Cancer Cell Immortalization Through Activation of Telomerase Activity Wang, Ruiguan Li, Jiangbo Zhang, Changjian Guan, Xin Qin, Boyu Jin, Rui Qin, Lingmei Xu, Shanrong Zhang, Xiaona Liu, Rong Ye, Qinong Cheng, Long Front Oncol Oncology Telomerase activity is elevated in most cancer cells and is required for telomere length maintenance and immortalization of cancer cells. Glucose metabolic reprogramming is a hallmark of cancer and accompanied with increased expression of key metabolic enzymes. Whether these enzymes influence telomerase activity and cell immortalization remains unclear. In the current study, we screened metabolic enzymes using telomerase activity assay and identified lactate dehydrogenase B (LDHB) as a regulator of telomerase activity. Sodium lactate and sodium pyruvate did not influence telomerase activity, indicating LDHB regulates telomerase activity independent of its metabolism regulating function. Further studies revealed that LDHB directly interacted with TERT and regulated the interaction between TERT and TERC. Additionally, long-term knockdown of LDHB inhibited cancer cell growth and induced cell senescence in vitro and in vivo. Higher LDHB expression was detected in pancreatic cancer tissues compared with that in adjacent normal tissues and expression of LDHB correlated negatively with prognosis. Thus, we identified LDHB as the first glucose metabolic enzyme contributing to telomerase activity and pancreatic cancer cell immortalization. Frontiers Media S.A. 2022-05-20 /pmc/articles/PMC9163669/ /pubmed/35669414 http://dx.doi.org/10.3389/fonc.2022.821620 Text en Copyright © 2022 Wang, Li, Zhang, Guan, Qin, Jin, Qin, Xu, Zhang, Liu, Ye and Cheng https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Wang, Ruiguan
Li, Jiangbo
Zhang, Changjian
Guan, Xin
Qin, Boyu
Jin, Rui
Qin, Lingmei
Xu, Shanrong
Zhang, Xiaona
Liu, Rong
Ye, Qinong
Cheng, Long
Lactate Dehydrogenase B Is Required for Pancreatic Cancer Cell Immortalization Through Activation of Telomerase Activity
title Lactate Dehydrogenase B Is Required for Pancreatic Cancer Cell Immortalization Through Activation of Telomerase Activity
title_full Lactate Dehydrogenase B Is Required for Pancreatic Cancer Cell Immortalization Through Activation of Telomerase Activity
title_fullStr Lactate Dehydrogenase B Is Required for Pancreatic Cancer Cell Immortalization Through Activation of Telomerase Activity
title_full_unstemmed Lactate Dehydrogenase B Is Required for Pancreatic Cancer Cell Immortalization Through Activation of Telomerase Activity
title_short Lactate Dehydrogenase B Is Required for Pancreatic Cancer Cell Immortalization Through Activation of Telomerase Activity
title_sort lactate dehydrogenase b is required for pancreatic cancer cell immortalization through activation of telomerase activity
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9163669/
https://www.ncbi.nlm.nih.gov/pubmed/35669414
http://dx.doi.org/10.3389/fonc.2022.821620
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