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

Abstract
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.
AuthorsRuiguan Wang, Jiangbo Li, Changjian Zhang, Xin Guan, Boyu Qin, Rui Jin, Lingmei Qin, Shanrong Xu, Xiaona Zhang, Rong Liu, Qinong Ye, Long Cheng
JournalFrontiers in oncology (Front Oncol) Vol. 12 Pg. 821620 ( 2022) ISSN: 2234-943X [Print] Switzerland
PMID35669414 (Publication Type: Journal Article)
CopyrightCopyright © 2022 Wang, Li, Zhang, Guan, Qin, Jin, Qin, Xu, Zhang, Liu, Ye and Cheng.

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