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TRIB3 Promotes Lung Adenocarcinoma Progression via an Enhanced Warburg Effect

BACKGROUND: The pseudokinase Tribbles 3 (TRIB3) is involved in many cellular processes and various cancers. In recent years, the importance of metabolic transformation in the maintenance of malignant tumors has become increasingly prominent. Abnormal metabolism of cancer cells is considered a hallma...

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Autores principales: Xing, Yutong, Luo, Peng, Hu, Rui, Wang, Duanduan, Zhou, Gang, Jiang, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7767749/
https://www.ncbi.nlm.nih.gov/pubmed/33380827
http://dx.doi.org/10.2147/CMAR.S287956
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author Xing, Yutong
Luo, Peng
Hu, Rui
Wang, Duanduan
Zhou, Gang
Jiang, Jie
author_facet Xing, Yutong
Luo, Peng
Hu, Rui
Wang, Duanduan
Zhou, Gang
Jiang, Jie
author_sort Xing, Yutong
collection PubMed
description BACKGROUND: The pseudokinase Tribbles 3 (TRIB3) is involved in many cellular processes and various cancers. In recent years, the importance of metabolic transformation in the maintenance of malignant tumors has become increasingly prominent. Abnormal metabolism of cancer cells is considered a hallmark of cancer. However, the exact role and molecular mechanism of TRIB3 in lung adenocarcinoma (LUAD) cell reprogramming is largely unknown. METHODS: The oxygen consumption rate (OCR) and extracellular acidification rate (ECAR) of cells were examined with a Seahorse XF Extracellular Flux Analyzer. In vitro and in vivo RT-qPCR, Western blotting, and functional assays were performed to explore the functional roles of TRIB3 in LUAD. RESULTS: In the present study, we demonstrated that TRIB3 is remarkably upregulated in LUAD cell lines as well as tissues. TRIB3 knockdown significantly inhibited LUAD cell growth and suppressed LUAD cell invasion, while TRIB3 overexpression conferred the opposite effects. Moreover, silencing TRIB3 suppressed the tumorigenesis and metastatic ability of LUAD cells. Mechanistically, we demonstrated that silencing TRIB3 significantly impaired aerobic glycolysis ability in LUAD cells. Furthermore, our data indicated that TRIB3 knockdown decreased hypoxia-inducible factor (HIF)1α levels and targeted the glycolytic genes regulated by HIF1α. CONCLUSION: Together, our findings revealed a previously unappreciated function of TRIB3 in cancer cell metabolism and tumor progression, illustrating that TRIB3 could be considered a valuable therapeutic target for LUAD patients.
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spelling pubmed-77677492020-12-29 TRIB3 Promotes Lung Adenocarcinoma Progression via an Enhanced Warburg Effect Xing, Yutong Luo, Peng Hu, Rui Wang, Duanduan Zhou, Gang Jiang, Jie Cancer Manag Res Original Research BACKGROUND: The pseudokinase Tribbles 3 (TRIB3) is involved in many cellular processes and various cancers. In recent years, the importance of metabolic transformation in the maintenance of malignant tumors has become increasingly prominent. Abnormal metabolism of cancer cells is considered a hallmark of cancer. However, the exact role and molecular mechanism of TRIB3 in lung adenocarcinoma (LUAD) cell reprogramming is largely unknown. METHODS: The oxygen consumption rate (OCR) and extracellular acidification rate (ECAR) of cells were examined with a Seahorse XF Extracellular Flux Analyzer. In vitro and in vivo RT-qPCR, Western blotting, and functional assays were performed to explore the functional roles of TRIB3 in LUAD. RESULTS: In the present study, we demonstrated that TRIB3 is remarkably upregulated in LUAD cell lines as well as tissues. TRIB3 knockdown significantly inhibited LUAD cell growth and suppressed LUAD cell invasion, while TRIB3 overexpression conferred the opposite effects. Moreover, silencing TRIB3 suppressed the tumorigenesis and metastatic ability of LUAD cells. Mechanistically, we demonstrated that silencing TRIB3 significantly impaired aerobic glycolysis ability in LUAD cells. Furthermore, our data indicated that TRIB3 knockdown decreased hypoxia-inducible factor (HIF)1α levels and targeted the glycolytic genes regulated by HIF1α. CONCLUSION: Together, our findings revealed a previously unappreciated function of TRIB3 in cancer cell metabolism and tumor progression, illustrating that TRIB3 could be considered a valuable therapeutic target for LUAD patients. Dove 2020-12-23 /pmc/articles/PMC7767749/ /pubmed/33380827 http://dx.doi.org/10.2147/CMAR.S287956 Text en © 2020 Xing et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Xing, Yutong
Luo, Peng
Hu, Rui
Wang, Duanduan
Zhou, Gang
Jiang, Jie
TRIB3 Promotes Lung Adenocarcinoma Progression via an Enhanced Warburg Effect
title TRIB3 Promotes Lung Adenocarcinoma Progression via an Enhanced Warburg Effect
title_full TRIB3 Promotes Lung Adenocarcinoma Progression via an Enhanced Warburg Effect
title_fullStr TRIB3 Promotes Lung Adenocarcinoma Progression via an Enhanced Warburg Effect
title_full_unstemmed TRIB3 Promotes Lung Adenocarcinoma Progression via an Enhanced Warburg Effect
title_short TRIB3 Promotes Lung Adenocarcinoma Progression via an Enhanced Warburg Effect
title_sort trib3 promotes lung adenocarcinoma progression via an enhanced warburg effect
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7767749/
https://www.ncbi.nlm.nih.gov/pubmed/33380827
http://dx.doi.org/10.2147/CMAR.S287956
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